A Förster Resonance Energy Transfer (FRET)-based System Provides Insight into the Ordered Assembly of Yeast Septin Hetero-octamers*

Background: Septins self-assemble into hetero-octameric rods and higher order structures and recruit other proteins. Results: A spectroscopic method (FRET) to measure septin interactions and binding of associated proteins was developed. Conclusion: End to end polymerization of Cdc11-capped rods, heterotypic end to end junctions between Cdc11-capped rods and Shs1-capped rods, and binding of an associated protein were demonstrated. Significance: This spectroscopic assay provides new insights about these polymeric proteins.


Prior studies in both budding yeast (Saccharomyces cerevisiae) and in human cells have established that septin protomers
assemble into linear hetero-octameric rods with 2-fold rotational symmetry. In mitotically growing yeast cells, five septin subunits are expressed (Cdc3, Cdc10, Cdc11, Cdc12, and Shs1) and assemble into two types of rods that differ only in their terminal subunit: Cdc11-Cdc12-Cdc3-Cdc10-Cdc10-Cdc3-Cdc12-Cdc11 and Shs1-Cdc12-Cdc3-Cdc10-Cdc10-Cdc3-Cdc12-Shs1. EM analysis has shown that, under low salt conditions, the Cdc11-capped rods polymerize end to end to form long paired filaments, whereas Shs1-capped rods form arcs, spirals, and rings. To develop a facile method to study septin polymerization in vitro, we exploited our previous work in which we generated septin complexes in which all endogenous cysteine (Cys) residues were eliminated by site-directed mutagenesis, except an introduced E294C mutation in Cdc11 in these experiments. Mixing samples of a preparation of such single-Cys containing Cdc11-capped rods that have been separately derivatized with organic dyes that serve as donor and acceptor, respectively, for FRET provided a spectroscopic method to monitor filament assembly mediated by Cdc11-Cdc11 interaction and to measure its affinity under specified conditions. Modifications of this same FRET scheme also allow us to assess whether Shs1-capped rods are capable of end to end association either with themselves or with Cdc11-capped rods. This FRET approach also was used to follow the binding to septin filaments of a septin-interacting protein, the type II myosin-binding protein Bni5.
Septins are a family of GTP-binding proteins found in all eukaryotes (except plants) (1,2) and have roles in cytokinesis, cell compartmentation, and membrane remodeling (3)(4)(5). The Saccharomyces cerevisiae genome encodes five septins that are expressed in mitotically growing cells: Cdc3, Cdc10, Cdc11, Cdc12, and Shs1 (6,7). Four of these proteins were first identified because the corresponding loci were among the temperature-sensitive cell division cycle (cdc) mutations isolated by Hartwell et al. (8,9) and specifically exhibited failure of cytokinesis at the restrictive temperature. The fifth member was identified later by other means and recognized as a gene product homologous to the other four (10,11).
During initial characterization of the cdc mutants by EM, it was noted that, after incubation of cells at the restrictive temperature, the cdc3, cdc10, cdc11, and cdc12 mutants uniquely lost filament-like striations found at the bud neck in control cells (12). These striations were 10 nm wide and ϳ28 nm apart. Indirect immunofluorescence with anti-septin antibodies (13)(14)(15) and, later, fusion of septins to fluorescent proteins (16,17) demonstrated that septins are located at and likely constituents of the filamentous bud neck structure. Subsequently, purification of septins from yeast (18) and as recombinant proteins from bacteria (19 -21) showed that Cdc3, Cdc10, Cdc11, and Cdc12 were sufficient to form long paired filaments in vitro (22) that closely resemble those seen by EM at bud neck in vivo (12,23,24).
Ensuing work showed that the five mitotic septins of yeast form two types of linear, apolar hetero-octameric complexes of a defined order, which differ only with respect to the terminal subunit present: Cdc11-Cdc12-Cdc3-Cdc10-Cdc10-Cdc3-Cdc12-Cdc11 and Shs1-Cdc12-Cdc3-Cdc10-Cdc10-Cdc3-Cdc12-Shs1 (22,25). These two types of rods are very stable, even in high salt (Ն250 mM) buffers. When the salt concentration is reduced (Ͻ100 mM), Cdc11-capped rods polymerize end to end into long paired filaments, as visualized in vitro by EM (22) and by super-resolution fluorescence microscopy (26). By contrast, Shs1-capped rods associate laterally in a staggered manner generating bundles that interact to form arcs, spirals, and rings (25). The septin collar at the bud neck appears to have three primary functions: (i) it establishes a cortical diffusion barrier (27,28); (ii) it serves as a scaffold to recruit other proteins (29,30); and (iii) it promotes membrane curvature either directly by deforming the membrane and/or indirectly by recruiting other proteins that can remodel membranes (31)(32)(33).
As for yeast, members of the family of 13 human septins also form linear hetero-octameric rods, the most abundant of which has the composition Sept9-Sept7-Sept6-Sept2-Sept2-Sept6-Sept7-Sept9 (34,35). Moreover, crystal structures of individual human septins (36,37) or septins from other animal cells (38) and of a human hetero-hexameric complex (39,40) revealed the nature of the two alternating interfaces that mediate linear assembly of the protomers into the hetero-oligomeric rod. The G interface between two subunits is an en face interaction that involves residues in and around the GTP-binding pockets of each protomer, and at the opposing surface (180°away from the G interface), is the NC interface wherein two subunits associate via contacts provided by residues in and around the N-and C-terminal segments of each protomer (39). Biochemical analysis (19,41) and structural studies (38,40) have shown how GTP binding, and, in the case of certain septin subunits, GTP hydrolysis, influences subunit conformation and interaction. In the yeast hetero-octamer, the Cdc11-Cdc12 interface is a G interface, the Cdc12-Cdc3 interface is an NC interface, and so forth (see Fig. 1A). Aside from their globular GTP-binding fold, the yeast mitotic septins have N-terminal extensions of variable length, with Cdc11 the shortest (12 residues) and Cdc3 the longest (110 residues), and, with the exception of Cdc10, also possess a long (Ն100 residue) flexible C-terminal extension (CTE) 5 that contains a segment (ϳ40 residues) with a strongly predicted propensity for coiled-coil formation (20,42).
To date, septin function in vivo has been studied primarily using genetic methods, and septin properties in vitro have been studied largely by examining static structures under the EM. Fluorescence microscopy has been used to visualize septin polymerization, but because of the large dimensions of the fluorophores used, either antibodies for immunostaining (20) or fusions to GFP (43) or to the SNAP tag (44), and the diffraction limit of light, such approaches cannot address the molecular details of the mechanism of septin assembly. Furthermore, given the dimensions of the yeast septin hetero-octamer (4 ϫ 32 nm), even super-resolution fluorescence microscopy applied to yeast septin filaments has merely confirmed what is already known about the order of subunits in the hetero-octamer (26).
To understand other self-assembling biopolymers, such as formation of microtubules from tubulin (45,46) and of F-actin from G-actin (47,48), and the interaction of these cytoskeletal elements with other proteins that bind to them, it has been exceedingly valuable to have spectroscopic assays to monitor the state of assembly in real time under conditions that can be readily manipulated. For the purposes of interrogating interactions at the protein-protein level, FRET is especially well suited. FRET allows for rapid measurements and is sensitive to the distance between the donor and acceptor fluorophores at the Յ10 nanometer scale, and the donor-acceptor/quencher interaction provides an unambiguous indication of how two elements within the system under study are associating. Given the hetero-oligomeric nature of septin complexes, we felt that FRET could provide a robust and sensitive means to investigate under a wide range of experimental conditions important and heretofore inaccessible mechanistic details about the dynamics and affinities of the protein-protein interactions involved in assembly and organization of septin structures.
Here we describe our development of a reliable FRET-based system for studying the polymerization of septin complexes into filaments, the effects of ionic strength on septin filament assembly, the interplay between Cdc11-and Shs1-capped hetero-octamers, the effects of mutational perturbation of important structural elements in the protomers on their ability to assemble, and the binding of a septin-associated protein. Our findings have important implications for understanding the physiological roles of alternate septin subunits and how septins behave as a polymeric system.

Experimental Procedures
Expression and Purification of Septin Complexes-Septin subunits were co-expressed from two DUET TM vectors (EMD Millipore) with compatible origins of replication essentially as described previously (20), except that Escherichia coli NiCo21 (DE3) (New England Biolabs) was used as the production strain because it has been engineered to prevent recovery of GlmS and several other endogenous E. coli Ni 2ϩ bead-binding proteins that are normally major contaminants in purifications utilizing IMAC (49). Prior work from this laboratory demonstrated that the Cys-less septins Cdc3(C124V,C253V,C279V), Cdc10(C266S), Cdc11(C43F,C137A,C138A), (His) 6 -Cdc12(C40A,C278S), and Shs1(C29V,C148S) supported yeast cell viability and formed recombinant hetero-octameric complexes that were indistinguishable in their in vitro assembly properties from those produced from their wild-type counterparts (50). Using a combination of standard site-directed mutagenesis (51) and sequence-and ligation-independent cloning (52), derivatives of each of the Cys-less septins were constructed in which a single Cys was reinstalled at a selected position. A pACYC plasmid expressing Cdc3(C124V,C253V,C279V) and Cdc11(C42F,C137A,C138A, E294C,⌬303-415) (50) was repaired to restore an intact CTE (residues 303-415) to the CDC11 ORF. A pACYC plasmid that expresses Cdc3(C124V,C253V,C279V) and Shs1(C29V, C148S,E344C) was constructed for production and purification of Shs1-capped hetero-octamers. Bacterial cultures were grown to an A 600 nm ϭ 0.8 -1.0, induced with isopropyl-␤-D-thiogalactoside (final concentration, 0.5 mM) overnight at 16°C, collected by centrifugation, and resuspended in ice-cold lysis buffer ( Fractions containing the bulk of the purified septin complexes were combined, and the resulting pool (typically 5-6 ml) was passed over chitin-agarose beads (New England BioLabs) to remove three other endogenous E. coli gene products (ArnA, SlyD, and Can) that are other known contaminants in IMAC-based purifications (because, in E. coli NiCo21 (DE3), each of these gene products has been tagged with a chitin-binding domain). The septin complexes in the flow-through from the chitin-agarose were loaded using the 10-ml loop of an AKTA FPLC system (GE Healthcare) onto a Superdex 200 HiLoad 16/60 column (16 mm ϫ 60 cm) (GE Healthcare) and subjected to size exclusion chromatography in septin buffer (300 mM KCl, 50 mM Tris-HCl (final pH 8.0)). Fractions were collected, and the proteins present in each were resolved by SDS-PAGE and visualized by staining with Coomassie Blue dye. The peak fractions containing the highest concentrations of stoichiometric septin complexes were pooled and used immediately for labeling by maleimide chemistry. Expression and Purification of Bni5-Using the sequenceand ligation-independent cloning procedure, the yeast BNI5 ORF was inserted in-frame with an N-terminal His 8 tag followed by a human rhinovirus 3C protease cleavage site in the bacterial expression vector pH3c-LIC, in which transcription is driven by the phage T7 promoter and regulated in an isopropyl ␤-D-thiogalactopyranoside-dependent manner by a lacO element. This vector was introduced into E. coli NiCo21 (DE3), and the cells were induced and lysed, and the Bni5 protein was purified by IMAC, chitin-agarose, and size exclusion chromatography, essentially as described above for the bacterially expressed septin complexes.
Maleimide Labeling-The protein concentration of the purified septin complexes (or Bni5) was determined using the bicinchoninic acid method (Pierce BCA protein assay kit; Life Technologies, Inc.) (53). Samples (typically, 2-4 g) were incubated with a 10-fold molar excess of reducing agent tris-(2-carboxyethyl)phosphine for 10 min at room temperature, desalted by passage through Sephadex G25 (8.3 ml; PD-10 column; GE Healthcare) in labeling buffer (300 mM KCl, 50 mM Tris (final pH 7.0)) to remove the tris-(2-carboxyethyl)phosphine, and labeled overnight at 4°C with a 5-fold molar excess of the desired maleimide dye (AF488, AF555, and AF647; Life Technologies, Inc.). Excess dye was reacted with a 10-fold molar excess of DTT at room temperature for 10 min and removed by recapturing the (His) 6 -Cdc12-containing septin complex by IMAC chromatography on a HisTrap HP column (GE Healthcare) (wash buffer: 300 mM KCl, 20 mM imidazole, 50 mM Tris-HCl (final pH 8.0); elution buffer: 300 mM KCl, 500 mM imidazole, 50 mM Tris-HCl (final pH 8.0)). The dye-labeled protein was dialyzed overnight against septin buffer (300 mM KCl, 50 mM Tris-HCl (final pH 8.0)) in a Slide-A-Lyzer dialysis cassette (Life Technologies, Inc.) with a 10-kDa molecular weight cutoff. The BCA assay (corrected for the contribution of the dye) and measurement of fluorescence using a P-330 Nanophotometer (Implen) were used to determine the molar concentration of protein and dye, respectively, in the final sample. In these complexes, in which only a single protomer type, e.g. Cdc11, contains the sole Cys present, the efficiency of labeling was 0.7-0.8 dye molecules per this subunit. Labeling of only the proper protomer was verified by resolving the subunits by SDS-PAGE and analyzing them by imaging with a Typhoon Trio Variable Mode Imager equipped for fluorescence (GE Healthcare) to detect the dye and by staining with Coomassie Blue dye and examining with an Odyssey scanner (Licor Biosciences) to detect the protein. Using the same criteria, the labeling efficiency for Bni5, which contains three native cysteines, was 2.7 dye molecules per protein.
Spectroscopy and Data Analysis-Absorbance spectra of 25 nM donor dye (AF555)-labeled septin hetero-octamers alone, serial dilutions of 100 nM acceptor dye (AF647)-labeled septin hetero-octamers alone (unless otherwise specified), and mixtures of the two were measured, in triplicate, at room temperature after equilibration for 1 h in a cuvette (3-mm path length, 270-l maximum volume) using a Cary Eclipse fluorescence spectrophotometer (Agilent). Unless specified otherwise, the final buffer conditions were 45 mM KCl, 50 mM Tris-HCl (pH 8.0). FRET values were obtained by subtracting the buffer-only background and correcting the emission of the acceptor at 671 nm for the contributions of both the donor and acceptor excited at 555 nM. The values reported represent the averages (ϮS.E.) of the triplicate samples. PCA (54) and subsequent data fitting was done using Matlab (The Mathworks) and its toolboxes for curve fitting and statistics. Alternately, semiquantitative sensitized emission techniques were used to obtain corrected FRET values, as previously described (55)(56)(57).
Fluorescence Microscopy-Microscope slides (3 inch ϫ 1 inch ϫ 1 mm) and coverslips (#1.5, 22 mm ϫ 22 mm) were bathed in 2 M HCl for 30 min, rinsed five times in double distilled H 2 O (15 min per wash), rinsed once in ethanol, and airdried. To coat the coverslip, 300 l of 1 mg/ml poly-L-lysine was pipetted onto its surface, and after incubation for 30 -60 min, it was rinsed twice with double distilled H 2 O, and air-dried. Purified septin complexes labeled with AF488 and AF555, respectively, were mixed and diluted to final concentration of 20 nM in 45 mM KCl, 50 mM Tris-HCl (pH 8.0) and incubated for 1 h at room temperature while protected from light. Samples (30 l) of the resulting septin filament-containing solution were pipetted onto the coverslip and followed immediately by 200 l of the same buffer to help disperse the protein more uniformly. The filaments were allowed to adhere to the poly-L-lysine surface for 30 min and then mounted on slides for imaging. The samples were viewed at room temperature using an Olympus IX81 microscope equipped with a 100X PlanApo Oil objective (numerical aperture 1.4, ∞/0.17) and an ORCA-ER CCD camera (Hamamatsu Photonics) (64.5 nm effective pixel size) controlled by MetaMorph (Molecular Devices). For AF488-labeled septins, an HQ 480/40 nm excitation filter and Q 505 long pass and HQ 535/50 nm emission filters were used (Chroma Technology Corp.). For AF555-labeled septins, an HQ 565-nm long pass and HQ 620/60-nm emission filters (Chroma Technology Corp.) were used. Unless otherwise specified, in all micrographs the scale bar represents 10 m.

Results
End to End Assembly of Donor-and Acceptor-labeled Cdc11capped Septin Hetero-octamers-Cdc11 is known to be the terminal subunit at each end of yeast septin hetero-octamers (22), which we have modeled on the basis of available crystal structures of mammalian septin complexes (37,39,40) using Phyre2 (58) (Fig. 1A). Prior work (18,22,59) has demonstrated that, in low salt buffer, native septin hetero-octamers assemble end on end via formation of an NC interface between Cdc11 subunits at the ends of adjacent rods to form a long filament (Fig. 1B). During their assembly, such individual filaments pair laterally in a highly cooperative manner. This arrangement seemed highly favorable for assessing the Cdc11-Cdc11 interaction via FRET because when donor dye-labeled Cdc11-capped rods are mixed with an equimolar amount of acceptor dye-labeled Cdc11-capped rods, on average, 50% of the resulting Cdc11-Cdc11 junctions should represent donor-acceptor pairs (Fig.  1B).
We selected as the donor-acceptor dye pair AF555 and AF647, two well characterized fluorophores, quite similar to Cy3 and Cy5, a well known FRET pair (60). As required for efficient FRET, the emission of the donor (AF555) shows good spectral overlap with the absorbance of the acceptor (AF647), with only a very modest tailing into the emission of the acceptor (Fig.  1C). Moreover, according to the manufacturer (Life Technologies, Inc.), the distance for 50% energy transfer (R 0 ) between these two dyes is 5.1 nm, and, based on our modeling, at the Cdc11-Cdc11 NC interface, dye attached to E294C in the CTE of one Cdc11 protomer should approach the dye attached to E294C in the CTE of the other Cdc11 protomer at a distance of ϳ3 nm. To test these predictions, a preparation of otherwise Cys-less septin complexes containing Cdc11(E294C) was labeled with AF555 ( Fig. 1D, upper panels), and another sample of the same complexes was labeled with AF647 ( Fig. 1D, lower panels). Indeed, when increasing amounts of the acceptor dye-labeled rods were mixed with a fixed concentration of donorlabeled rods and excited only at the absorbance of the donor, the characteristic spectral features of FRET were clearly observed: a diminution of the donor emission with a concomitant and corresponding increase in emission from the acceptor (Fig. 1E), as also confirmed by PCA analysis (Fig.  1E, inset). The fact that only one principal component could be detected in the FRET spectrum (unless otherwise noted, this principal component accounted for Ͼ98% of the variability in our system) indicates that the FRET observed arises from the predicted bimolecular interaction of donor dyelabeled Cdc11 and acceptor dye-labeled Cdc11 at the Cdc11-Cdc11 junctions between rods and not from dye-dye interactions across the individual strands in paired filaments or other possible modalities, which would be expected to generate additional principal components.
Aside from revealing FRET arising from the expected close approach of donor-labeled Cdc11 and acceptor-labeled Cdc11 at the ends of the hetero-octamers, such titration experiments yield binding curves when replotted as the maximal corrected FRET observed at each of the known concentrations of acceptor dye-labeled rods that were added to the fixed known concentration of donor dye-labeled rods (Fig. 1F). Indeed, the expected approach to saturation was observed because the probability of formation of a FRET-competent Cdc11-Cdc11 junction between a donor dye-labeled rod and an acceptor dyelabeled rod should increase as the ratio of acceptor dye-labeled rods to donor dye-labeled rods increases. In addition, this very reproducible behavior indicates, contrary to indirect experiments suggesting the opposite (61), that, once assembled, a hetero-octamer is remarkably stable, i.e. subunits in different rods do not dissociate, intermix, and reassemble, at least over the time scale of our experiments. Moreover, assuming stochastic polymerization of donor-and acceptor-labeled rods, we could estimate the fraction of donor dye-labeled Cdc11-capped rods in end to end association with acceptor dye-labeled Cdc11-capped rods as the ratio of the concentration of the acceptor complexes divided by the total septin present (donor and acceptor complexes). In this way, such saturation curves (Fig. 1F) (Table 1). Furthermore, assuming an "ideal" model, namely one Cdc11 binding to one Cdc11 (AB max ϭ 1) and a K d ϭ 25 nM for that interaction, generated a binding isotherm nearly identical to the observed saturation curve (Fig.  1F), fully consistent with the FRET arising purely from end to end assembly of donor-and acceptor-labeled Cdc11-capped septin hetero-octamers.
Linear Organization of Septin Hetero-octamers-FRET can be used not only as a read-out for close association of a donorand an acceptor-labeled molecule, but can also serve as a "molecular ruler" because the FRET efficiency (E) is strongly dependent on the distance between the donor and the acceptor (r), as well as on the 50% transfer distance (R 0 ) for the dye pair used, where F DA is the fluorescence intensity of the donor with the acceptor present, and F D is the fluorescence intensity of the donor alone (Equation 1) (62).
Given the fixed order of subunits in yeast septin hetero-octamers demonstrated both in vitro (22) and in vivo (63), the observed FRET between any given donor dye-labeled septin subunit and another acceptor-dye labeled protomer should be reproducibly sensitive to its position within the rod (Fig. 2B).
Again, to test the reliability of our system to exhibit this expected behavior, a preparation of otherwise Cys-less heterooctamers containing Cdc11(E294C) labeled with the donor AF555 was titrated with preparations of otherwise Cys-less hetero-octamers containing, respectively, Cdc11(E294C), Cdc12(L310C), Cdc3(S407C), or Cdc10(R298C) that were labeled with the acceptor AF647 (Fig. 2C). As anticipated, we observed that FRET efficiency between Cdc11-Cdc11 donoracceptor pairs was higher than for Cdc11-Cdc12, Cdc11-Cdc3, and Cdc11-Cdc10 donor acceptor pairs. The observed FRET efficiencies were used to calculate experimentally derived distances and plotted against those values (Fig. 2D). Although no crystal structure yet exists for S. cerevisiae septin complexes, our homology model (Fig. 1A) and the known diameter (4 nm) of the globular GTP-binding domain of yeast septin subunits estimated from EM (22) allowed us to predict, based on end to end assembly, the approximate distance between the positions of the fluorophores in the different septin pairs: Cdc11-Cdc11, ϳ2.6 nm; Cdc11-Cdc12, ϳ8.3 nm; Cdc11-Cdc3, ϳ10.8 nm; and Cdc10, ϳ16.7 nm. The experimentally derived values certainly follow the same trend as these predicted distances.
Especially noteworthy in this regard, however, was our finding that the calculated Cdc11-Cdc12 (5.02 nm) and Cdc11-Cdc3 (5.08 nm) distances were very similar. In the labeled Cdc12 and Cdc3 hetero-octamers, the acceptor dye is located near the base of the predicted ␣6 helix of the CTEs of these subunits, and ample evidence both in vitro and in vivo indicates that the CTEs of Cdc3 and Cdc12 are entwined in a coiled-coil interaction (22,42,59,64). Given the position at which these acceptor dyes were installed, the fact that the measured distance between the Cdc11-Cdc12 and Cdc11-Cdc3 fluorophores was so similar suggests that, relative to the donor dye in Cdc11, the acceptor dyes in Cdc12 and Cdc3 are located in very close proximity to each other. This observation is consistent with and provides additional physical evidence for the presence of an intimate coiled-coil interaction between the CTEs of Cdc12 and Cdc3. As expected, there was a marked decrease in FRET between the terminal subunit (Cdc11) and the protomer (Cdc10) situated at the greatest distance away at the center of the rod (Fig. 2D).
Although the observed FRET values displayed a clear distance sensitivity, the experimentally calculated lengths deviated significantly from those predicted from our modeling. However, the "expected" distances were based on modeling against a rather low resolution (ϳ4 Å) crystal structure of mammalian septins (39). Also, our measurements were made using pairs of donor and acceptor fluorophores located at the very end of the ␣6 helix, which terminates the GTP-binding domain, at its junction with the long flexible CTE; thus, this position may have a significantly greater range of mobility than predicted. Finally, in vivo, septin rods assemble into filament-like structures on the cytosolic surface of the plasma membrane; however, when the septin rods assemble into filament-like structures in solution, they have a tendency to bundle laterally upon prolonged incubation or at a sufficiently high concentration (22,44,59). In principle, this bundling could contribute to the differences seen between the "expected" distances predicted by our modeling and the length values derived from our FRET measurements, if, for example, some filaments in such bundles were staggered (i.e. out of perfect register). Our fluorescence micrographs indicate that bundling occurs under our polymerization conditions (see supplemental Figs. S1-S4).
Effect of Ionic Strength on the Cdc11-Cdc11 NC Interface-There is ample evidence that septin filaments disassemble at high ionic strength into their constituent hetero-octamers (18,20,21) and, conversely, that polymerization of Cdc11-capped hetero-octamers into long paired filaments is favored at low ionic strength (22,59). Thus, if our FRET system is reliably reporting filament assembly, the observed energy transfer between our donor dye-labeled Cdc11-capped rods and acceptor dye-labeled Cdc11-capped rods should be greatly diminished when the ionic strength is raised above the threshold required to disrupt the Cdc11-Cdc11 interaction. Indeed, when our standard titrations of donor-labeled rods with acceptorlabeled rods were conducted in buffers of increasing salt (KCl) concentration (Fig. 3A), the maximum observed FRET was progressively diminished, displaying a rather sharp transition with an EC 50 of ϳ180 mM KCl (Fig. 3B), exhibiting an apparent Hill coefficient above 5 ( Table 2) and raising the K d app from 20 to 30 nM to a value so weak and irreproducible (Ͼ Ͼ100 nM) that it was not possible to measure accurately (Fig. 3C).
Novel Insights about the Behavior of Shs1-capped Heterooctamers-Aside from Cdc3, Cdc10, Cdc11, and Cdc12, mitotically growing yeast cells express a fifth septin, Shs1 (551 residues), that is most closely related to but 33% larger than Cdc11 (415 residues). Prior work has demonstrated that Shs1 can replace Cdc11 and thus serve as an alternative terminal subunit in yeast septin hetero-octamers (25). Indeed, like Cdc11capped hetero-octamers (Fig. 4A, lower panels), we were able to prepare stable, otherwise Cys-less septin complexes containing Shs1(E344C) that we could efficiently label with either the donor AF555 or acceptor AF647 dyes (Fig. 4A, upper panels). These reagents allowed us to address several previously unresolved questions about the properties of such Shs1-capped rods.
First, EM imaging indicates that, in low salt buffers, Shs1capped hetero-octamers bundle and form rather thick arcs, rings, spirals, and bird's nest-like arrangements (25). Given the density of these structures, it has not been possible to discern definitively whether or not Shs1-capped hetero-octamers have any capacity to join end on end via an Shs1-Shs1 NC interface. To address this question, a fixed concentration of donor dyelabeled Shs1(E344C)-containing rods was titrated with increasing concentrations of acceptor dye-labeled Shs1(E344C)-containing rods. Unlike the robust FRET observed for the such donor-acceptor titrations with Cdc11-capped rods (Fig. 1E), no detectable FRET occurred in the Shs1-Shs1 donor-acceptor mixtures, as evidenced by the fact that there was no internally consistent decrease in the emission of the donor and no corresponding enhancement in the emission of the acceptor above the background contribution of its increasing concentration (Fig. 4B). Thus, as judged by this criterion, Shs1-capped hetero-octamers are unable to engage in any persistent end on end association. Moreover, PCA of the spectral data showed two distinct principal components (Fig. 4B, inset), suggesting that the spectra recorded arise from at least two classes of weak fluorophore interactions, consistent with the complex structures formed by Shs1-capped hetero-octamers on EM grids (25). Indeed, even at the macroscopic level of the fluorescence microscope, fluorescently tagged Shs1-capped complexes formed curved structures and even some rings (supplemental Fig. S1, left panel).
Second, it has been shown biochemically that purified Shs1 can associate with purified Cdc11 in vitro (20) and, as viewed in the EM, that titering a solution of Shs1-capped hetero-octamers with increasing amounts of Cdc11-capped hetero-octamers widens the diameter and thins out the edges of the rings formed from Shs1-capped complexes, suggesting that Cdc11-capped rods can intercalate in some fashion into structures composed of Shs1-capped rods and alter their supramolecular organization (25). These findings suggest that Cdc11-capped complexes and Shs1-capped complexes might be able to form heterotypic NC junctions. Consistent with this conclusion, we recently provided genetic evidence that such heterotypic NC junctions likely occur in the cell (65). However, there previously has been no direct and incisive means to confirm that Shs1-capped hetero-octamers are able to form heterotypic NC junctions with Cdc11-capped hetero-octamers. To test this possibility directly, we titrated several fixed concentrations of donor dyelabeled Shs1-capped rods with increasing concentrations of acceptor dye-labeled Cdc11-capped rods. In marked contrast to the Shs1-Shs1 donor-acceptor mixtures, the Shs1 donor-Cdc11 acceptor mixtures exhibited robust FRET (Fig. 4C), equivalent to that displayed by Cdc11-Cdc11 donor-acceptor mixtures (Figs. 1F and 2A). The average K d app value for the Shs1-Cdc11 interaction derived from these binding curves was ϳ20 nM Ϯ 10 nM (range) (Table 1), a slightly higher affinity than measured for the Cdc11-Cdc11 NC interaction. Likewise, the effect of increasing salt concentration on the stability of the Shs1-Cdc11 association displayed a somewhat broader transition and a somewhat higher EC 50 of ϳ200 mM KCl than for the Cdc11-Cdc11 interaction (Table 2), again consistent with the Shs1-Cdc11 interaction being somewhat tighter than the Cdc11-Cdc11 interaction. Thus, we conclude that Shs1-capped  hetero-octamers are indeed able to engage in a heterotypic end on end interaction with Cdc11-capped hetero-octamers. Interestingly, at the macroscopic level, in 1:1 mixtures of fluorescently tagged Shs1-capped septin complexes and Cdc11-capped septin complexes, the two dyes are clearly incorporated into the same structures (supplemental Figs. S2A and S4 A); however, the Shs1-containing regions are discontinuous and appear embedded within a more continuous matrix of Cdc11-containing regions (supplemental Figs. S2A and S4A, white arrowheads). This organization could reflect the demonstrated capacity of Shs1-capped hetero-octamers for lateral bundling (25), such that even if an Shs1-capped rod is incorporated into these structures via its end to end association with Cdc11-capped rods, it could still nucleate lateral binding of additional Shs1-capped rods at the same location, resulting in the observed puncta. Presumably, the properties of such mixed assemblies give septin-based structures the flexibility and plasticity necessary to form the lattice-and gauze-like arrangements, and other supramolecular architectures, that have been observed in cells by freeze-fracture (66), cryo-electron tomography (23), and other EM methods (24).

Analysis of the Role of Conserved Structural Elements in Septin-Septin
Interaction-In the original x-ray structure of the human Sept7-Sept6-Sept2-Sept2-Sept6-Sept7 hetero-hexamer, each subunit was truncated to remove its CTE to promote crystallization (39), so no information about the disposition of those structural elements (Fig. 1A, arrows) was provided. Subsequently, the isolated CTEs of these same septins have been studied as purified recombinant proteins in solution, and it has been reported that the CTEs of Sept6 and Sept7 (equivalent to yeast Cdc3 and Cdc12, respectively) are able to form an elongated heterodimer with high ␣-helical content (presumably, a coiled coil) with a K d of 15.8 nM (67). This value is in the same range as the Cdc11-Cdc11 and Shs1-Cdc11 interactions shown here. Moreover, although cells in which either cdc11(⌬CTE) or shs1(⌬CTE) mutants are expressed as sole source of these septins are viable, their growth and morphology are not normal (20,64). Hence, we sought to assess the contributions of the corresponding CTEs of Cdc11 and Shs1 to Cdc11-Cdc11 homotypic and Shs1-Cdc11 heterotypic association. Cdc11 and Shs1 contain CTEs that are similar, apart from a 45-residue insert (residues 401-446) found in Shs1. Removal of the CTE (residues 306 -415) from Cdc11 or of the CTE (residues 349 -551) from Shs1 did not affect the engineered Cys in ␣6 (E294C in Cdc11 and E344C in Shs1, respectively) that we used for maleimide labeling and do not affect the formation of stable hetero-octameric complexes (25,50). Hence, we prepared, labeled and analyzed otherwise Cys-less complexes containing either Cdc11(E294C ⌬CTE) or Shs1(E344C ⌬CTE) (Fig.  5A). We found that absence of the CTE from Cdc11 in the acceptor dye-labeled rods or from both the donor dye-labeled rods and the acceptor dye-labeled rods did not have a significant effect on the FRET observed (Fig. 5B) or on the K d app value for the Cdc11-Cdc11 interaction derived from such binding curves (Table 3). Likewise, we found that removal of the CTE from Shs1 or from Cdc11 or from both did not have a significant effect on the FRET observed (Fig. 5C) or on the K d app value for the Shs11-Cdc11 interaction derived from such binding  (Table 3). Likewise, at the macroscopic level, fluorescently tagged hetero-octamers capped with Cdc11(⌬CTE) formed polymerized structures with either Cdc11-capped hetero-octamers or Cdc11(⌬CTE)-capped hetero-octamers with equal efficiency (supplemental Fig. S3, B and C). Similarly, the presence or absence of the CTE on Shs1 or Cdc11, or both, did not prevent the formation of colocalized polymerized structures closely resembling those formed between intact Shs1-capped and intact Cdc11-capped septin complexes (supplemental Fig. S2, B-D). These results are consistent with our recent genetic evidence that, unlike heterodimeric coiled coil formation by the CTEs of Cdc3 and Cdc12 that contributes to the strength of their interaction (20,22,59), the CTEs of Cdc11 and Shs1 do not make a major contribution to either Cdc11-Cdc11 or Shs1-Cdc11 interaction but rather contribute to the efficiency of recruitment in vivo of at least one septinassociated protein to the septin-containing structures at the bud neck (65).
Another helical element, ␣0, observed in the crystal structure of a human Sept2-Sept2 NC dimer (39), contributes some residues to the buried surface at this interface (39) and has been implicated previously in the strength of septin-septin interaction both in vitro (22) and in vivo (63). However, a tract of basic residues found within ␣0 also appears to be sufficiently surfaceexposed so as to contribute to the association of septin complexes with phosphatidylinositol 4,5-bisphosphate in the plasma membrane (59,64,68). Sequence alignments and modeling indicate that all of the yeast mitotic septins have an ␣0. The apparent ␣0 in Cdc11 and Shs1 corresponds to residues 6 -19 and 7-20, respectively. As analyzed by deposition onto carbon-coated grids and examination in the EM, septin heterooctamers capped with Cdc11(⌬2-18), which removes essentially the entire ␣0 hence, termed Cdc11(⌬␣0), were unable to polymerize in solution into filaments (22). In marked contrast, hetero-octamers capped with Cdc11(⌬␣0) were able to assemble end on end to form filaments when polymerized on the surface of a PtdIns4, 5P 2 -containing lipid monolayer (59), indicating some significant residual capacity of the Cdc11(⌬␣0)capped rods to associate via the Cdc11-Cdc11 NC interface.
To explore this question further, we prepared, labeled, and analyzed otherwise Cys-less complexes containing either Cdc11(⌬␣0 E294C) or Shs1(⌬2-18/⌬␣0 E344C) (Fig. 6A). Titrating Cdc11-capped donor dye-labeled rods with Cdc11(⌬␣0) acceptor dye-labeled rods yielded FRET behavior and an apparent affinity for Cdc11-Cdc11 interaction that was indistinguishable from that observed with wild-type Cdc11 acceptor dye-labeled rods ( Fig. 6B and Table 4); however, when ␣0 was absent from the Cdc11 in both the donor dye-labeled rods and the acceptor dye-labeled rods, there was a modest, but measurable, reduction in the apparent strength of the Cdc11-Cdc11 interaction (Fig. 6B and Table 4). Similarly, when mixtures of Shs1-capped complexes and Cdc11-capped complexes were examined, the most striking effect was observed upon removal of ␣0 from Shs1 in donor dye-labeled complexes, which weakened the K d app value for the Shs1-Cdc11 interaction by 4 -5-fold ( Fig. 6C and Table 4); however, the noise in these particular measurements makes this value only very approximate. Nonetheless, when both Shs1 and Cdc11 lacked ␣0, interaction strength was improved ( Fig. 6C and Table 4). PCA (not shown) of the same spectral data indicated maintenance of a single principal component in all these mutant combinations, supporting the view that 1:1 Cdc11-Cdc11 and Shs1-Cdc11 interactions were still able to occur in vitro even when these subunits lack their ␣0 element. Thus, it appears that those residues of ␣0 thought to be buried at the NC interface do not contribute in a major way to the binding energy of this interaction, at least in solution.
However, our complementary analysis of the ability of these fluorophore-labeled complexes to assembly into higher order structures at the macroscopic level, as assessed by fluorescence microscopy, provided evidence that Cdc11 and Shs1 lacking their ␣0 are less stable and have a tendency to mis-or unfold, as FIGURE 5. Effect of deletion of the terminal subunit C-terminal extension on septin octamer assembly by FRET. A, Coomassie gels and typhoon scans of labeled septin octamers with AF555 and AF647 using end subunits of Shs1 ⌬CTE and Cdc11 ⌬CTE. B, binding curves for Cdc11 AF555 -Cdc11 AF647 (red), Cdc11 AF555 -Cdc11 ⌬CTE AF647 (cyan), and Cdc11 ⌬CTE AF555 -Cdc11 ⌬CTE AF647 (magenta). C, binding curves for Shs1 AF555 -Cdc11 AF647 (red), Shs1 AF555 -Cdc11 ⌬CTE AF647 (cyan), Shs1 ⌬CTE AF555 -Cdc11 AF647 (magenta), and Shs1 ⌬CTE AF555 -Cdc11 ⌬CTE AF647 (black). For B and C, dots represent measured data, and colorcoded lines represent the corresponding binding curve fit.  Fig. S3, D and E). Similarly, in the case of mixtures of Shs1-capped complexes with Cdc11-capped complexes, removal of ␣0 from either or both of these septins altered their ability to form the higher order structures observed with complexes capped with their wild-type counterparts. When Cdc11(⌬␣0) complexes were combined with Shs1 complexes, there was less colocalization of Cdc11(⌬␣0) with Shs1 and an increase in the formation of Shs1-containing puncta (supplemental Fig. S4B). Conversely, Shs1(⌬␣0) complexes combined with Cdc11 complexes exhibited increased colocalization, suggesting that removal of ␣0 from Shs1 permits its more facile integration into Cdc11-containing structures (supplemental Fig. S4C). When Shs1(⌬␣0) complexes were combined with Cdc11(⌬␣0) complexes, however, very few organized structures of any sort were formed from either septin-containing complex (supplemental Fig. S4D). These findings could be best explained by a role for ␣0 in maintaining the stable three-dimensional fold in both Cdc11 and Shs1.
Binding and Localization of a Septin-associated Protein-In addition to its use in monitoring assembly of fluorophore-labeled building blocks into a polymeric structure and its utility in gauging approximate distances among fluorophore-labeled constituents of multiprotein complexes, FRET can also be used to determine whether an exogenously added, heterologous protein can associate with a pre-existing complex and the binding affinity and preferred binding site of that interaction. To test the utility of our system for this purpose, we examined the asso-ciation of four derivatives of Cdc11-capped septin complexes, each donor dye-labeled on one of its component subunits and assembled into filaments at low salt concentration, with acceptor dye-labeled Bni5.
BNI5 was isolated as a dosage suppressor of cdc12-6 and other temperature-sensitive septin mutants, and yeast two-hybrid analysis in vivo and GST pulldown assays in vitro indicated that Bni5 physically associates most strongly with Cdc11 (69). Subsequent work has demonstrated that Bni5 serves as an adaptor to link septin filaments at the bud neck to the yeast type II myosin (Myo1) necessary for contractile ring formation prior to cytokinesis (65,70,71).
As an initial test, we labeled purified native Bni5, which contains three endogenous Cys (Cys-144, Cys-266, and Cys-375), with the acceptor dye (Fig. 7A). The efficiency with which we were able to label Bni5 with acceptor dye (2.7 AF647 molecules per protein) indicates that all three of Cys residues are solventexposed, consistent perhaps with structural predictions, suggesting that Bni5 is a very elongated, nearly all-␣-helical protein (65). Because of the multiple dyes present, we anticipated that if FRET was observed between the acceptor-labeled Bni5 and the donor dye-labeled septin filaments, any values obtained from it for apparent affinity and distance estimates would only be approximate. Nonetheless, we found that acceptor dye-labeled Bni5 showed readily detectable FRET with septin filaments containing donor dye-labeled Cdc11 and progressively lower FRET with septin filaments where the donor dye was located on another subunit (Fig. 7B), in agreement with all of the prior evidence that Bni5 associates preferentially with Cdc11 in Cdc11-capped hetero-octamers. The K d app derived for the Bni5-Cdc11 interaction from multiple titrations of donor dyelabeled Cdc11(E294C)-containing filaments was ϳ200 nM (Fig.  7C). This apparent affinity is in remarkably good agreement with a value (ϳ300 nM) reported for binding of Bni5 to septin complexes measured by the technique of surface plasmon resonance (44).

FRET Provides a Versatile Assay for Monitoring Septin
Mechanics-Prior to this work, the only assay available to observe septin assembly in vitro was by visual inspection of septins tagged by fusion to large genetically encoded fluoro-FIGURE 6. Effect of deletion of the terminal subunit ␣0 helix on septin octamer assembly by FRET. A, Coomassie gels and typhoon scans of labeled septin octamers with AF555 and AF647 using end subunits of Shs1 ⌬␣0 and Cdc11 ⌬␣0. B, binding curves for Cdc11 AF555 -Cdc11 AF647 (red), Cdc11 AF555 -Cdc11 ⌬␣0 AF647 (cyan), and Cdc11 ⌬␣0 AF555 -Cdc11 ⌬␣0 AF647 (magenta). C, binding curves for Shs1 AF555 -Cdc11 AF647 (red), Shs1 AF555 -Cdc11 ⌬␣0 AF647 (cyan), Shs1 ⌬␣0 AF555 -Cdc11 AF647 (magenta), and Shs1 ⌬␣0 AF555 -Cdc11 ⌬␣0 AF647 (black). For B and C, dots represent measured data, and color-coded lines represent the corresponding binding curve fit. genic proteins under the fluorescence microscope (43). Although this technique is useful to observe the dynamics of formation of septin structures on a large scale, the proteinprotein interactions intimately involved in the mechanism of septin assembly at the nanometer scale are inaccessible at the level of resolution of fluorescence microscopy. By contrast, our development of a FRET-based method enabled us to address detailed questions about the assembly mechanics and subunit interactions in septin complexes. One major benefit of FRET is that the efficiency of the energy transfer between small, organic dye fluorophores is dependent on the distance between them in a predictable fashion and on scales relevant for septin biology. Thus, by placing FRET-compatible fluorophores on different combinations of subunits, we were able to provide independent confirmation that Cdc11capped septin hetero-octamers assemble into filaments by end on end formation of homotypic Cdc11-Cdc11 junctions and not via any other sort of subunit-subunit interactions. Our measurements also provide the first quantitative estimate of the strength of the Cdc11-Cdc11 NC interface, which has a remarkably high affinity (K d app ϭ ϳ30 nM). Moreover, we were able to demonstrate, conversely and for the first time, that Shs1-capped hetero-octamers are incapable of engaging in end on end association via homotypic Shs1-Shs1 interaction. Revealingly, however, and yet again for the first time, our FRET method showed that Shs1-capped hetero-octamers are capable of engaging in heterotypic Shs1-Cdc11 junctions, as had been inferred from purely circumstantial evidence based on genetic arguments in our prior studies (65). Currently, there is no evidence either in vitro (25) or in vivo (25,63,64,73) that a heteroctamer can be heterotypically capped with a Cdc11 at one end and Shs1 at the other. Moreover, at a more macroscopic scale, we found that these Shs1-Cdc11 junctions are formed at a distinctly lower frequency than Cdc11-Cdc11 because Shs1capped rods are incorporated within higher order Cdc11-containing structures in a highly dispersed and irregularly periodic manner. This behavior is in keeping with one of the likely physiologic roles for incorporation of Shs1-capped hetero-octamers into the filaments composed of Cdc11-capped hetero-octamers, namely to assist in imparting curvature to generate and control the diameter of the septin rings at the bud neck, whose size changes during progression through the yeast cell division cycle (24,32). This hypothesis is supported by experiments in which changing the relative stoichiometry of Shs1-and Cdc11capped hetero-octamers altered the diameter and thickness of rings observed under the EM (25) and by the fact that although shs1⌬ mutants are viable, the efficiency of cytokinesis in such cells is clearly compromised (73,74).
Conditions Influencing Septin Filament Assembly-A valuable feature of our FRET-based assay and another advantage over studies conducted using fluorescence microscopy is that it is readily accessible to manipulation of the solvent conditions. There are many parameters that could affect septin assembly that might also be regulated in the cell, such as the guanine nucleotide concentration or pH.
Here, however, we chose to examine the effect of ionic strength because of its well characterized influence on the state of septin filament assembly in vitro demonstrated in prior work (18,22). Using our FRET system, we found that the ability of Cdc11-capped rods to polymerize end on end into filaments is indeed salt-sensitive. The transition between filaments and isolated rods was very sharp (an apparent Hill coefficient Ͼ5) and occurred at an EC 50 for the molarity of KCl just slightly higher (ϳ180 mM) than that thought to represent the tonicity inside cells (equivalent to 120 -150 mM) (75). This finding suggests that, at the ionic strength inside cells, the rod to filament equilibrium may be poised to be ultrasensitive to changes in other septin effectors (e.g. changes in the concentrations of particular septin subunits, GTP, and/or septin-associated proteins, or changes in post-translational modifications on septin or septinassociated proteins). If so, it would give cells the capacity to rapidly remodel septin-based structures in response to the appropriate cellular cues. Indeed, the septin cytoskeleton undergoes a variety of dramatic structural changes as the cell cycle proceeds: formation of a septin cap or nascent hoop at the incipient bud site in late G 1 ; expansion/extension of the hoop into an hourglass-shaped collar in S to late anaphase; splitting or collapse of the collar into two bands at the onset of cytokinesis; and breakdown of all observable higher order septin structure prior to initiation of the next cell cycle (29,30).
In further regard to the effect of ionic strength and given that previous observations in our own and in other laboratories have shown that septin hetero-octamers themselves are remarkably stable even at salt concentrations as high as 300 -500 mM NaCl or KCl (18, 20 -22), the salt-sensitive interaction responsible for salt-induced filament disassembly is clearly the Cdc11-Cdc11 NC interface. In this same regard, and given that our FRET approach was able to definitely show that Shs1-Cdc11 NC junctions are able to form robustly and have an apparent affinity (K d app ϳ20 nM) even greater than Cdc11-Cdc11 junctions, it is tempting to speculate that the reported extensive and cell cycle-dependent phosphorylation of Shs1 (76,77), which does not appear to be required for Shs1 function per se (64), occurs as a means to enhance the efficiency of disassembly of the residual septin filaments and rings at the bud neck at the end of each cell cycle.
Analysis of Conserved Structural Elements in Septin Organization-In addition to examining the properties of wildtype septin complexes, we also used our FRET methodology to explore the effect of altering certain recognized structural elements in septin monomers on the assembly properties of hetero-octamers containing them. Here, in particular, we probed the roles of the CTE and ␣0 helix in Cdc11 and in Shs1 in the formation of both homotypic Cdc11-Cdc11 interaction and in heterotypic Shs1-Cdc11 association.
Deletion of the CTE, even when removed from Cdc11 in both the donor dye-labeled Cdc11-capped complexes and the acceptor dye-labeled Cdc11 capped complexes, did not prevent formation of homotypic Cdc11-Cdc11 NC junctions or affect their apparent affinity. Likewise, deletion of the CTE from either Shs1 or Cdc11, or both, did not significantly perturb formation of heterotypic the Shs1-Cdc11 NC junction. Thus, the CTEs of Cdc11 and Shs1 do not contribute to either the Cdc11-Cdc11 or the Shs1-Cdc11 interaction, consistent with recent genetic evidence that these CTEs serve instead to enhance the recruitment of at least one septin-associated protein (65).
Our FRET system also allowed us to interrogate and answer a lingering issue about another structural element, ␣0, thought to reside at the NC interface. However, there have been conflicting views about the degree to which ␣0 is buried or solventexposed and how much it contributes to the strength of the NC interaction (39,63,64). We found that removal of the ␣0 helix had no major effect on K d app for either the Cdc11-Cdc11 or the Shs1-Cdc11 interaction. Indeed, as first shown using lipid monolayers on EM grids to capture septin filament polymerization (59), hetero-octamers capped with Cdc11(⌬␣0) retain the capacity to assemble into filaments, in contradiction to earlier work (22) in which similar preparations were examined for filament assembly in solution by then depositing the material on EM grids for visualizing by negative staining in the EM. Thus, our findings agree with the more recent data. It is possible that the original discrepancy arose because in the earlier study preformed filaments may have disassembled under the conditions required for processing of the samples, which involved solutions of heavy metals that have a high ionic strength.
Moreover, we found (see images in supplemental Figs. S1-S4) that upon assembly, hetero-octamers capped with Cdc11(⌬␣0) have a much greater tendency than hetero-octamers capped with wild-type Cdc11 to accumulate puncta and form larger order aggregates, and in the original study, such structures (because they did not resemble long paired filaments) may have been overlooked. In any event, our findings indicate that a lack of the ␣0 helix destabilizes Cdc11 and Shs1, resulting in a greater propensity for these subunits to undergo unfolding or misfolding.
Furthermore, in agreement with our FRET results indicating little direct role for the ␣0 helix in formation of the Cdc11-Cdc11 or Shs1-Cdc11 NC interfaces, there is ample evidence that the tract of basic residues in the ␣0 helix of mitotic septin subunits Cdc10 (59), Cdc11, and Shs1 (63,64) is sufficiently solvent-exposed to contribute to the interaction of septin filaments with phosphatidylinositol 4,5-bisphosphate in the plasma membrane and is required for the biological function of these septins in vivo. It should be conceded that one drawback of our FRET method in solution, as it presently stands, is that it cannot assess interactions of septins with membranes or membrane surrogates.
Binding of a Septin-associated Protein-Finally, we demonstrated that we could apply our FRET approach to delineate the affinity of binding and the location of binding of a septin filament-associated protein. There are a plethora of gene products that, when GFP-tagged, localize to the yeast bud neck (29,78), but in only a very few cases has it been determined which of these proteins physically associates directly with a septin or is localized at the bud neck indirectly by steric trapping or through association with the plasma membrane or with another protein that does bind directly to a septin. Our FRET method, because it uses purified components, can distinguish between these two extremes for any bud neck-localized protein that can be expressed and purified as a recombinant protein or purified to homogeneity from yeast cells.
In this regard and as a test case, we examined the association of Bni5 (Bud neck-interacting protein 5) (69). We found, using our FRET assay, that Bni5 is indeed capable of binding directly to septin filaments and shows a strong preference for association with Cdc11, in agreement with results obtained by others using different in vivo and in vitro methods. Moreover, our analysis yielded a K d app value for the Bni5-Cdc11 interaction (ϳ200 nM) quite similar to that (ϳ300 nM) obtained by a completely different and independent biophysical method conducted by others (44). Preparing single-Cys derivatives of Bni5 will allow refinement of our binding curves to obtain more accurate assessment of its affinity and, especially, its orientation at its binding site. Furthermore, our FRET approach can be extended to defining by mutagenesis the residues in both Bni5 and Cdc11 that are essential for their high affinity interaction. Clearly, our system can be extended to interrogate any septin-interacting protein to determine the affinity of its binding, to pinpoint which septin subunit constitutes its preferred binding partner, and to determine its orientation relative to other landmarks in the hetero-octamer, such as the edge from which all the CTEs project or the opposite edge (Fig. 1A). Indeed, in this regard, we have available functional single-Cys substitutions situated at various positions in and around the surface of each of the mitotic subunits (50) that could be used systematically to acquire information about such distance constraints. Similarly, with proper stopped flow instrumentation, our FRET assay could be modified to obtain kinetic parameters for polymerization of septin hetero-octamers into filaments and to determine the rate of association of septin-binding proteins with filaments. Finally, with the proof of principle we have provided here, our FRET-based techniques could also be extended to analyze the much more complex interplay among the 13 different human septin subunits and their multifarious splice variants and other isoforms (5,79) and to address the organization and polymerization behavior of the complexes comprising them. Past work with other biopolymers, such as actin (72), has shown that the combination of spectroscopy with microscopy is exceedingly powerful for determining structure-function relationships. Relative to other cytoskeletal biopolymers, techniques for studying septins have been more rudimentary. We hope that the establishment of our FRET-based assay will provide a platform for greater understanding of how septins, their binding partners, and their regulatory factors are linked to the biological functions of these fascinating proteins.