Mechanism of frataxin “bypass” in human iron–sulfur cluster biosynthesis with implications for Friedreich's ataxia

In humans, mitochondrial iron–sulfur cluster biosynthesis is an essential biochemical process mediated by the assembly complex consisting of cysteine desulfurase (NFS1), LYR protein (ISD11), acyl-carrier protein (ACP), and the iron–sulfur cluster assembly scaffold protein (ISCU2). The protein frataxin (FXN) is an allosteric activator that binds the assembly complex and stimulates the cysteine desulfurase and iron–sulfur cluster assembly activities. FXN depletion causes loss of activity of iron–sulfur-dependent enzymes and the development of the neurodegenerative disease Friedreich's ataxia. Recently, a mutation that suppressed the loss of the FXN homolog in Saccharomyces cerevisiae was identified that encodes an amino acid substitution equivalent to the human variant ISCU2 M140I. Here, we developed iron–sulfur cluster synthesis and transfer functional assays and determined that the human ISCU2 M140I variant can substitute for FXN in accelerating the rate of iron–sulfur cluster formation on the monothiol glutaredoxin (GRX5) acceptor protein. Incorporation of both FXN and the M140I substitution had an additive effect, suggesting an acceleration of distinct steps in iron–sulfur cluster biogenesis. In contrast to the canonical role of FXN in stimulating the formation of [2Fe–2S]–ISCU2 intermediates, we found here that the M140I substitution in ISCU2 promotes the transfer of iron–sulfur clusters to GRX5. Together, these results reveal an unexpected mechanism that replaces FXN-based stimulation of the iron–sulfur cluster biosynthetic pathway and suggest new strategies to overcome the loss of cellular FXN that may be relevant to the development of therapeutics for Friedreich's ataxia.

In humans, mitochondrial iron-sulfur cluster biosynthesis is an essential biochemical process mediated by the assembly complex consisting of cysteine desulfurase (NFS1), LYR protein (ISD11), acyl-carrier protein (ACP), and the iron-sulfur cluster assembly scaffold protein (ISCU2). The protein frataxin (FXN) is an allosteric activator that binds the assembly complex and stimulates the cysteine desulfurase and iron-sulfur cluster assembly activities. FXN depletion causes loss of activity of iron-sulfur-dependent enzymes and the development of the neurodegenerative disease Friedreich's ataxia. Recently, a mutation that suppressed the loss of the FXN homolog in Saccharomyces cerevisiae was identified that encodes an amino acid substitution equivalent to the human variant ISCU2 M140I. Here, we developed iron-sulfur cluster synthesis and transfer functional assays and determined that the human ISCU2 M140I variant can substitute for FXN in accelerating the rate of ironsulfur cluster formation on the monothiol glutaredoxin (GRX5) acceptor protein. Incorporation of both FXN and the M140I substitution had an additive effect, suggesting an acceleration of distinct steps in iron-sulfur cluster biogenesis. In contrast to the canonical role of FXN in stimulating the formation of [2Fe-2S]-ISCU2 intermediates, we found here that the M140I substitution in ISCU2 promotes the transfer of iron-sulfur clusters to GRX5. Together, these results reveal an unexpected mechanism that replaces FXN-based stimulation of the iron-sulfur cluster biosynthetic pathway and suggest new strategies to overcome the loss of cellular FXN that may be relevant to the development of therapeutics for Friedreich's ataxia.
Iron-sulfur clusters are ubiquitous protein cofactors that are required for critical cellular processes (1,2). Iron-sulfur clus-ters exist in a variety of stoichiometries, most often as [2Fe-2S] 2ϩ/1ϩ and [4Fe-4S] 2ϩ/1ϩ species, and commonly function in substrate activation and in electron transfer. Iron-sulfur clusters are synthesized and distributed to apo target proteins by conserved biosynthetic pathways. In humans, an assembly complex located in the mitochondrial matrix is responsible for synthesizing iron-sulfur clusters (3,4). The structural core of this assembly complex consists of cysteine desulfurase (NFS1), eukaryotic-specific LYR protein (ISD11), and acyl carrier protein (ACP) subunits and is referred to as the SDA (or SDA ec if it includes Escherichia coli ACP; Table 1) 5 complex (5,6). The ISD11 and ACP subunits are required for function, stabilize NFS1, and favor different quaternary interactions for NFS1 than its prokaryotic homologs (6 -10). NFS1 uses a pyridoxal 5Ј-phosphate cofactor to convert L-cysteine to L-alanine and generate a persulfide intermediate on a cysteine residue of a mobile S-transfer loop (Fig. 1, step 1). Sulfur is then transferred from NFS1 to a cysteine residue on the scaffold protein ISCU2 (Fig. 1, step 2). ISCU2 combines the sulfane sulfur from persulfide intermediates with Fe 2ϩ and electrons to produce [2Fe-2S] 2ϩ clusters (11)(12)(13) (Fig. 1, step 3) in a poorly understood process. To complete catalytic turnover, intact [2Fe-2S] cluster intermediates on ISCU2 are transferred to a cluster carrier protein, such as the monothiol glutaredoxin GRX5 (Fig. 1, step 4), as a part of the cluster distribution network.
An additional essential component of the eukaryotic ironsulfur assembly system is the protein frataxin (FXN). The loss of FXN function leads to iron accumulation in mitochondria, increased oxidative stress, and loss of activity of iron-sulfur enzymes and is associated with the fatal neurodegenerative disease Friedreich's ataxia (14 -17). FXN binds to the SDA ec U (SDA ec with ISCU2; Table 1) complex and accelerates ironsulfur cluster biosynthesis on the scaffold protein (18 -22). Initially, FXN was proposed to be an iron chaperone for ironsulfur cluster biosynthesis (23)(24)(25)(26). More recent evidence supports a role for FXN as an allosteric activator that facilitates sulfur transfer chemistry, which is associated with persulfide intermediates required for iron-sulfur cluster synthesis (12,20,27,28). The mechanism and molecular details of FXN binding and activation are still poorly understood.
Interestingly, a suppressor mutation affecting Saccharomyces cerevisiae Isu1 (homolog of human ISCU2; Isu1 M107I also known as Isu1 Sup ) was identified that rescues growth defects caused by the deletion of S. cerevisiae Yfh1 (homolog of human FXN) (29,30). Initial radiolabeling studies suggest that Isu1 Sup increases the accumulation of persulfide species on Nfs1 similar to the addition of FXN (12,27). In contrast, two subsequent studies using standard reconstituted assays of partial reactions failed to identify a mechanism by which the human ISCU2 M140I (equivalent to Isu1 Sup ) variant could functionally replace FXN in iron-sulfur cluster biosynthesis (31,32).
In this manuscript, new functional assays were developed, which include both iron-sulfur cluster synthesis and transfer reactions, to test the effect of the human ISCU2 M140I substitution on activity. We found that human ISCU2 M140I , like S. cerevisiae Isu1 Sup , accelerates iron-sulfur biosynthesis in the absence of FXN in complete reconstituted reactions. We also found that unlike FXN, which stimulates the cysteine desulfurase and [2Fe-2S] cluster biosynthetic reactions of the SDA ec U complex, the substitution of ISCU2 with ISCU2 M140I primarily affects the transfer rate of intact [2Fe-2S] clusters from ISCU2 to GRX5. Overall, our results provide new mechanistic insights and indicate that FXN and ISCU2 M140I function at distinct stages of the iron-sulfur cluster biosynthetic pathway.

ISCU2 and the ISCU2 M140I variant have similar biochemical properties
We purified native ISCU2 and the ISCU2 M140I variant and probed their secondary structure, oligomeric state, and ability to form iron-sulfur assembly complexes. ISCU2 and the ISCU2 M140I variant exhibited highly similar far UV CD spectra with negative ellipticity features at 208 and 222 nm and a positive feature at 193 nm, which are characteristic of ␣-helices (Fig.  S1). Analytical ultracentrifugation sedimentation velocity studies reveal that both ISCU2 and the ISCU2 M140I variant exist primarily as monomeric species in solution (Fig. 2). Next, the SDA ec U and SDA ec U M140I complexes were generated by com-bining recombinantly expressed human NFS1-ISD11 complex that copurified with E. coli ACP (SDA ec ) (6, 33) with ISCU2 or the ISCU2 M140I variant. To test for the ability of the iron-sulfur assembly complexes to bind FXN, the FXN S202C variant was purified, labeled with the Texas Red C2 fluorophore, and titrated with either the SDA ec U or SDA ec U M140I complex (Fig.  3). Changes in fluorescence anisotropy were fit to a binding equation and revealed that the FXN affinity to the complex is largely unaffected by the incorporation of the M140I substitution. Thus, the M140I substitution does not significantly affect the secondary structure and the oligomeric state of ISCU2 or its ability to form the activated iron-sulfur cluster assembly complex with SDA ec and FXN.

Both FXN and the ISCU2 M140I substitution accelerate the formation of [2Fe-2S] clusters on GRX5
We then tested whether iron-sulfur cluster assembly complexes in which human ISCU2 is substituted with the ISCU2 M140I variant can bypass the function of FXN in ironsulfur cluster biosynthesis. A visible CD assay was developed to monitor an entire iron-sulfur cluster assembly and transfer reaction (Fig. 1, steps 1-4). This region of the CD spectrum is sensitive to the iron-sulfur cluster chromophore and can be used to distinguish cofactor association with different proteins. This assay, unlike previously reported assays that only monitor intermediate formation on NFS1 or ISCU2, better represents the in vivo biosynthetic pathway by building iron-sulfur clusters in situ on the scaffold protein ISCU2 and then transferring these clusters to GRX5 to complete a catalytic cycle. This assay takes advantage of the positive ellipticity from [2Fe-2S]-GRX5 and low ellipticity from [2Fe-2S]-ISCU2 at 450 nm ( Fig. S2) to detect product formation. Reactions were initiated with the addition of L-cysteine and GSH, which is required for binding

FXN-independent activation of iron-sulfur cluster synthesis
the iron-sulfur cluster to GRX5. The SDA ec U, SDA ec U M140I , and SDA ec UF (SDA ec U plus FXN;  4 and Table 2), which were approximately three times greater than for the SDA ec U complex. The results from this in vitro iron-sulfur cluster biosynthetic assay are consistent with the stimulation of activity both by FXN and by ISCU2 M140I in the absence of FXN.

FXN and ISCU2 M140I operate at different steps in iron-sulfur cluster biosynthesis
We also tested the effect of adding FXN to the SDA ec U M140I complex in complete cluster assembly and transfer reactions ( Fig. 1, steps 1-4). The SDA ec U M140I F complex had a [2Fe-2S]-GRX5 formation rate that was greater than the SDA ec U complex (nearly 7-fold greater) and was approximately twice the rate of either the SDA ec UF or SDA ec U M140I complex ( Fig. 4 and Table 2). This additive result in the iron-sulfur assembly assay hints that the stimulatory effects of FXN and ISCU2 M140I occur at different steps in iron-sulfur cluster biosynthesis. Because FXN was previously shown to increase the rates of partial reactions, including the cysteine desulfurase activity of SDA ec U and the assembly of [2Fe-2S] cluster intermediates on ISCU2 (6, 20, 22), we tested whether ISCU2 M140I also affected those steps of iron-sulfur cluster biosynthesis.
The M140I substitution had minor effects on the cysteine desulfurase and iron-sulfur cluster synthesis (Fig. 1, steps 1-3) activities of the SDA ec U complex. SDA ec was previously shown to exhibit a low k cat (0.60 min Ϫ1 ) for the cysteine desulfurase reaction (6), which was not affected by the addition of ISCU2 but was stimulated 10-fold by the inclusion of both ISCU2 and FXN (Table 2) (6,20). The SDA ec U M140I complex exhibited kinetic parameters similar to those of the SDA ec U complex, with a k cat 10-fold less than that of the SDA ec UF complex (Table 2 and Fig. 5). The addition of FXN to the SDA ec U M140I complex stimulated cysteine turnover in a manner reminiscent of the WT system. Thus, the M140I variant behaves almost identically to ISCU2 in the cysteine desulfurase assay.
Next, the ISCU2 M140I variant was tested for its ability to mimic FXN in increasing the rate of [2Fe-2S] cluster formation on ISCU2. CD spectroscopy was used to monitor [2Fe-2S] cluster formation on ISCU2 and ISCU2 M140I by following changes in ellipticity at 330 nm, similar to a previously reported assay (22). Here, we show the addition of FXN to the SDA ec U complex accelerates iron-sulfur cluster formation on ISCU2  Table 2). The SDA ec U M140I complex exhibited 1.5 times greater cluster synthesis activity than the native SDA ec U complex but only approximately half the activity of SDA ec UF. The addition of FXN to the SDA ec U M140I complex further enhanced its activity (1.5-fold greater), consistent with FXN stimulation of the native system. Overall, the additive effects in complete synthesis and transfer assays coupled to the inability of ISCU2 M140I to fully replace FXN in stimulating cysteine desulfurase and iron-sulfur assembly reactions are consistent with FXN and ISCU2 M140I affecting different steps of iron-sulfur cluster biosynthesis.

The ISCU2 M140I substitution accelerates cluster transfer to GRX5
Given that ISCU2 acts as a scaffold for [2Fe-2S] cluster synthesis and functions as an intermediate to transfer these clusters to target proteins, we evaluated the ability of FXN and the ISCU2 M140I substitution to affect the transfer of the [2Fe-2S] cluster intermediate from ISCU2 to GRX5 (Fig. 1, step 4). The SDA ec U and SDA ec U M140I complexes were incubated with L-cysteine and ferrous iron in the absence of GRX5, and the development of the characteristic [2Fe-2S]-ISCU2 CD spectrum was observed (Fig. S5). The reaction was allowed to progress for 160 min to ensure completion of the [2Fe-2S]-ISCU2 formation reaction. After 160 min, apo-GRX5 (with or without FXN) was added under anaerobic conditions (see arrow in   Fig. S6). The cluster transfer reaction from ISCU2 to GRX5 was then followed by monitoring the increase in ellipticity at 450 nm ( Fig. 6B and Fig. S6). The rates of cluster transfer for SDA ec U and SDA ec UF were the same within error ( Table 2), establishing that FXN does not have a role in cluster transfer under these conditions. In contrast, iron-sulfur assembly complexes containing the ISCU2 M140I variant transferred cluster at almost twice the rate of complexes with WT ISCU2.

FXN-independent activation of iron-sulfur cluster synthesis
One possible explanation for the enhanced transfer rate is the M140I substitution on ISCU2 could destabilize the [2Fe-2S] cluster to facilitate cluster exchange with GRX5. We therefore tested this possibility in three ways. First, we determined whether the incorporation of the M140I substitution affected the cluster equilibrium between ISCU2 and GRX5. Here, the ability of [2Fe-2S]-GRX5 to transfer its cluster to either excess apo-ISCU2 or apo-ISCU2 M140I was monitored by changes in the CD spectra (Fig. S7). No significant loss of [2Fe-2S]-GRX5 signal was observed for either reaction after 1 h (in the presence or absence of GSH), supporting an essentially irreversible [2Fe-2S] cluster transfer reaction from ISCU2 to GRX5.

FXN-independent activation of iron-sulfur cluster synthesis
Second, we used a SYPRO orange thermal stability assay to determine whether the M140I substitution affects the stability of ISCU2 in the presence or absence of a [2Fe-2S] cluster (Fig.  S8). The assay takes advantage of an increase in fluorescence that occurs upon protein denaturation and dye binding to hydrophobic residues. ISCU2 and ISCU2 M140I had similar melting temperatures with and without [2Fe-2S] cluster bound, suggesting that the M140I substitution does not greatly affect the stability of the apo or cluster bound state.
Third, we examined the susceptibility of [2Fe-2S]-ISCU2 and [2Fe-2S]-ISCU2 M140I to loss of their clusters in the presence of DTT. DTT promotes the loss and transfer of [2Fe-2S] clusters from ISCU2 (11,22). Here, iron-sulfur clusters were enzymatically generated on ISCU2 (or ISCU2 M140I ), and the holo-proteins were combined with DTT (Fig. S9). Both samples lost a majority of their cluster-dependent CD signal within 30 min with a slightly greater rate of cluster extrusion for ISCU2 than the ISCU2 M140I sample. These results indicate that the greater [2Fe-2S] cluster transfer rate for ISCU M140I samples is not simply due to decreased cluster stability on ISCU2. Overall, these studies indicate that the ISCU2 M140I substitution, but not FXN, affects the iron-sulfur cluster transfer reaction from ISCU2 to GRX5.

Discussion
Friedreich's ataxia is an incurable neurodegenerative disease associated with the loss of FXN function. The physiological role of FXN is still debated, and two primary proposals for its function in iron-sulfur cluster biosynthesis have emerged: a chaperone that delivers iron and an allosteric activator that stimulates sulfur-based chemistry. Recently, an ISU1 mutation that suppressed the growth defects of S. cerevisiae lacking the YFH1 homolog of FXN was identified (29,30). This result was puzzling because it was not clear how an amino acid substitution affecting Isu1 might mimic FXN and function as an iron chaperone or stimulate sulfur-based chemistry. Moreover, it was also unclear whether the analogous ISCU2 variant bypasses FXN function in the human iron-sulfur cluster biosynthetic system. Therefore, we decided to investigate whether the ISCU2 M140I substitution stimulates human iron-sulfur cluster biosynthetic activity, which might provide new mechanistic insight into FXN function and opportunities for developing Friedreich's ataxia therapeutics.
Our results, along with two recent studies (31,32), indicate that native ISCU2 and the ISCU2 M140I variant have similar biochemical and stability properties. First, we found that the M140I substitution does not affect the protein's secondary structure (Fig. S1), consistent with a recent finding by Yue and co-workers (31). In contrast, the Markley group reported different secondary structures for native ISCU2 and the ISCU2 M140I variant (32); similar differences have recently been correlated with apo and zinc-bound forms of ISCU2 (31). Second, we do not observe a significant difference between the stability of the as-isolated forms of ISCU2 and ISCU2 M140I (Fig.  S8), consistent with a previous study (31). Third, our results indicate that both ISCU2 and the M140I substitution exist as monomers in solution (Fig. 2). Finally, we find that the M140I substitution also does not dramatically affect the ability of ISCU2 to form the SDA ec UF complex (Fig. 3). We therefore concluded that the M140I substitution does not significantly alter the biochemical properties of ISCU2 and examined its effect on activity.
Incorporating the M140I substitution and generating the SDA ec U M140I complex does not replace FXN in stimulating the cysteine desulfurase and iron-sulfur cluster assembly reactions (Fig. 1, steps 1-3). The SDA ec U M140I complex has nearly identical cysteine desulfurase kinetic parameters and the ability to be stimulated by FXN as the SDA ec U complex (Table 2), consistent with recent activity measurements performed at a single substrate concentration (31,32). The lack of stimulation for the SDA ec U M140I complex compared with SDA ec U is surprising for two reasons. First, if this substitution mimicked FXN, we would expect a stimulation of activity for the SDA ec U M140I complex. Second, previous single-turnover experiments showed that Isu1 Sup increases the accumulation of persulfide label on Nfs1 in the S. cerevisiae system (30). It is unclear whether these different results and conclusions are due to the experimental systems (human versus yeast), the nature of the assays (multiturnover versus single turnover), or some other factor. Further, we found that complexes that contain the M140I substitution exhibit a modest (1.5-fold) increase in the rate of [2Fe-2S] cluster synthesis but were unable to fully reproduce the stimulation by FXN (2.8-fold). This result is again consistent with previous assays that showed iron-sulfur assembly complexes containing the M140I substitution are unable to replace the activation role of FXN in iron-sulfur cluster synthesis (32); quantitative comparisons between our CD-based results and these assays are challenging because their absorbance peak has contributions from [2Fe-2S] cluster synthesis on ISCU2, [2Fe-2S] cluster oxidation of FDX2, and potential formation of iron-sulfur mineral-like species (22). We find the M140I variant functions similar to ISCU2 and can be activated by FXN (Table 2), consistent with previous DTT-containing but not FDX2-containing assays (32). Overall, all three studies on human iron-sulfur assembly systems indicate that the M140I substitution on ISCU2 is unable to replace the role of FXN and stimulate cysteine desulfurase and iron-sulfur assembly reactions.
Here, we provide evidence that the M140I substitution unexpectedly affects the transfer of intact iron-sulfur clusters (Figs. 4 and 6 and Table 2). A new assay was developed that monitors the synthesis of [2Fe-2S] clusters on ISCU2 (Fig. 1, steps 1-3) and their subsequent cluster transfer to GRX5 (Fig. 1, step 4). Assembly complexes in which native ISCU2 was substituted with the M140I variant or supplemented with FXN accelerate the rate of [2Fe-2S] cluster formation on GRX5 by approximately a factor of three ( Fig. 4 and Table 2). Interestingly, when both the M140I substitution and FXN are included, the rate of cluster formation on GRX5 is further stimulated (6.6-fold; Table 2), suggesting that these effects occur at different steps of the pathway. In a separate experiment, we show that the M140I substitution, but not FXN, accelerates cluster transfer from ISCU2 to GRX5 (Fig. 6). Our working model is that the ratelimiting step in this biosynthetic system is a transfer of intact [2Fe-2S] clusters from ISCU2 to GRX5, which appears to be an essentially irreversible reaction (Fig. S7). The rate of this reaction is directly proportional to the amount of [2Fe-2S] cluster

FXN-independent activation of iron-sulfur cluster synthesis
on ISCU2 and the rate constant for cluster transfer to GRX5. Our data support a role for FXN in increasing the concentration of [2Fe-2S] cluster on ISCU2 and the M140I substitution in enhancing the rate constant for cluster transfer. This model explains why the effects of FXN and the ISCU2 M140I substitution are additive in this system and provides a possible mechanism for how Isu1 Sup may replace FXN function.
We then aimed to better understand how the M140I substitution might facilitate cluster transfer. First, we examined whether the [2Fe-2S] cluster bound to the M140I variant was inherently less stable, which might facilitate cluster transfer. However, a thermal stability assay revealed similar melting temperatures for the chemically reconstituted [2Fe-2S] cluster-bound forms of both proteins (Fig. S8). Second, we examined whether the [2Fe-2S] cluster binding equilibrium between ISCU2 and GRX5 was altered by the M140I substitution. There was very little, if any, back transfer of iron-sulfur clusters from [2Fe-2S]-GRX5 to either apo ISCU2 or the apo M140I variant (Fig. S7). Third, we tested the susceptibility of the [2Fe-2S] clusters to extrusion from the protein through the addition of DTT. A decrease in [2Fe-2S] cluster CD signal was observed in both cases, with the rate of signal loss slightly higher for ISCU2 than for the M140I variant (Fig. S9). Together, these results do not support a model in which decreased stability of the [2Fe-2S] cluster bound to the M140I variant promotes increased cluster transfer kinetics. Interestingly, residues other than isoleucine that have a higher hydropathy index (34) than methionine (valine and leucine) but not those with a lower index (threonine, proline, histidine, and glycine) are also able to replace FXN function (29). We hypothesize that during cluster transfer, the [2Fe-2S]-containing ISCU2 undergoes a conformational change, likely involving a hydrophobic residue at position 140, to an activated form that is critical for interactions with apo-GRX5 and lowering the activation energy for cluster transfer.
Overall, we demonstrate that the human ISCU2 M140I variant can overcome the loss of FXN function but, surprisingly, not by accelerating the same chemical step in iron-sulfur cluster biosynthesis. Our results indicate that the ISCU2 M140I variant accelerates the cluster transfer reaction from ISCU2 to GRX5 rather than mimicking the FXN role in stimulating iron-sulfur cluster assembly. These results provide new insight into ironsulfur cluster biosynthesis and suggest new potential strategies to overcome the loss of FXN function and treat Friedreich's ataxia.
The pHis-GFP-TEV-GRX5 plasmid was transformed into Rosetta (DE3) cells (VWR). The cells were grown in LB medium (VWR) at 37°C until the A 600 reached 0.5, and then ␤-D-1thiogalactopyranoside was added to a final concentration of 0.5 mM. The temperature was decreased to 16°C, and the cells were grown for an additional ϳ16 h. The harvested cell pellets were resuspended in buffer A (50 mM Tris and 250 mM NaCl at pH 7.5) with 5 mM imidazole and lysed by sonication (Branson sonifier 450). The soluble fraction was loaded on a nickelnitrilotriacetic acid column (5 ml; GE Life Sciences), and the his-GFP-TEV-GRX5 fusion was eluted using buffer A and a linear gradient between 5 and 500 mM imidazole. The green fractions were combined and dialyzed into buffer B (50 mM Tris, pH 7.5). The sample was then incubated overnight at room temperature with TEV protease (1:50 molar ratio of protease to fusion protein). The cleaved material was then loaded onto an anion exchange column (27 ml; 16 mm ϫ 13.5 cm, POROS HQ 50) and eluted with buffer B and a linear gradient from 0 to 1 M NaCl. The GRX5 fractions were concentrated and loaded onto a 26/60 Sephadex 100 column (GE Life Sciences) equilibrated with 50 mM HEPES and 150 mM NaCl at pH 7.5. Monomeric fractions with Ͼ 96% purity were concentrated, frozen in liquid nitrogen, and stored at Ϫ80°C.
Apo protein concentrations were estimated using the following extinction coefficients: SDA ec using 10.9 mM Ϫ1 cm Ϫ1 at 420 nm, ISCU2 using 8490 mM Ϫ1 cm Ϫ1 at 280 nm, FXN using 26030 mM Ϫ1 cm Ϫ1 at 280 nm, and GRX5 using 17780 mM Ϫ1 cm Ϫ1 at 280 nm (20,38). Protein variants were assumed to have the same extinction coefficient as the native proteins. The concentration of [2Fe-2S]-GRX5 was determined with a sulfidedetection assay (39). 10 and 20 l of as purified [2Fe-2S]-GRX5 was diluted to 800 l with buffer C and incubated at 37°C for 20 min. 100 l of 20 mM N,NЈ-diphenyl-p-phenylenediamine (in 7.2 M HCl) and 30 mM FeCl 3 (in 1.2 M HCl) were added, and the solutions were incubated at 37°C for 20 min. The samples were centrifuged at 10,000 ϫ g for 5 min, and the absorbance at 670 nm was converted to the concentration of sulfide using a standard curve. The concentration of sulfide was plotted against the amounts of sample, fit to a straight line through zero, and used to calculate the [2Fe-2S]-GRX5 concentration. Unless otherwise stated, all protein manipulations and reactions were carried out in an anaerobic glove box (MBRAUN; maintained at ϳ14°C with O 2 Ͻ 1 ppm). The molecular masses for proteins and protein complexes are provided in Table S1.

Oligomeric state of ISCU2 and ISCU2 M140I
Purified ISCU2 (300 l of 538 M) and ISCU2 M140I (400 l of 434 M) were passed through an analytical size-exclusion chromatography column (Superdex 200 10/300 GL, GE Healthcare Life Sciences) that was equilibrated in buffer C (50 mM HEPES, 250 mM NaCl, pH 7.5). Each protein eluted as a single peak that

FXN-independent activation of iron-sulfur cluster synthesis
was collected and concentrated. ISCU2 and ISCU2 M140I stock solutions were diluted with buffer C to produce 29.5 (A 280 ϭ 0.25) and 88.3 (A 280 ϭ 0.75) M samples. The 500 l samples were examined with sedimentation velocity analytical ultracentrifugation (AUC) experiments at 50,000 rpm at the Center for Analytical Ultracentrifugation of Macromolecular Assemblies under the University of Texas Health Science Center, San Antonio. The molar mass was estimated from the measured sedimentation and diffusion coefficients for each sample, using a partial specific volume based on the protein sequence of the analyte. The calculation was performed using the following for- where MW is the molar mass, R is the gas constant, T is the absolute temperature, s is the sedimentation coefficient corrected to 20°C in water, D is the diffusion coefficient corrected to 20°C in water, [macron]v is the partial specific volume, and is the solvent density. CRC Handbook of Chemistry and Physics reference values were used for viscosity and density. The v values of 0.746 ml/g for ISCU2 M140I and 0.744 ml/g for ISCU2 were calculated by Ultra-Scan (http://ultrascan2.uthscsa.edu/) (40). 6

Fluorescence anisotropy measurements
Because native FXN contains no cysteine residues, the FXN S202C variant was constructed for maleimide labeling. The FXN S202C variant (50 l of 1420 M) in buffer D (20 mM NaH 2 PO 4 , 150 mM NaCl, pH 7.2) was reacted with 10 l of a 9.84 mM solution of Texas Red TM C2 maleimide (TRM; Ther-moFisher) in 100% DMSO for 2 h. The excess fluorophore was removed using a 1-ml anion column (HiTrap Q HP, GE Healthcare Life Science). The concentration of FXN S202C in the labeled aliquot was determined using a Bradford assay (using purified FXN S202C as standard). The concentration of the TRM fluorophore in the labeled protein was determined using ⑀ 595 ϭ 112000 mM Ϫ1 cm Ϫ1 . The final concentration of TRM labeled FXN S202C was 18.5 M with a labeling efficiency of 55%.
The fluorophore-labeled FXN S202C (0.1 M) was combined with 100 M L-cysteine, 200 M Fe 2ϩ , and either 30 M ISCU2 or ISCU2 M140I . The samples were then incubated with different concentrations of the SDA ec complex for 15 min. The fluorescence was measured at room temperature with an excitation wavelength of 560 nm and perpendicular excitation polarizer and an emission wavelength of 605 nm with either a perpendicular or parallel emission polarizer (TECAN infinite F200 PRO

Complete iron-sulfur cluster synthesis and transfer reactions
The complete reaction assays included 0.5 M SDA ec , 20 M ISCU2 (or ISCU2 M140I ), 20 M (or 0 M) FXN, 40 M GRX5, and 400 M Fe(NH 4 ) 2 (SO 4 ) 2 and buffer E (50 mM HEPES, 150 mM KCl, and 10 mM MgCl 2 at pH 7.5). The reactions were initiated by the addition of 100 M L-cysteine and 10 mM GSH at room temperature. Cluster formation on GRX5 was then measured for SDA ec U, SDA ec UF, SDA ec U M140I , and SDA ec U M140I F by monitoring the ellipticity change at 450 nm using a Chirascan CD spectrometer (Applied Photophysics). Cuvettes (1-cm path length) were sealed with a rubber septum and electrical tape in a glove box. The kinetic data were fit to an exponential rise equation ([y ϭ y 0 ϩ A 0 ⅐(1 Ϫ exp(Ϫk⅐t))], where the k is the apparent rate of cluster formation on GRX5) using Kaleidagraph (Synergy Software, Reading, PA).

Cysteine desulfurase activity measurements
Cysteine desulfurase activities were measured for each complex using a slightly modified methylene blue assay (20,39).

Iron-sulfur cluster assembly reactions on ISCU2
Iron-sulfur assembly reactions on ISCU2 contained 10 M SDA ec , 30 M ISCU2 (or ISCU2 M140I ), 30 M FXN (when added), 400 M Fe(NH 4 ) 2 (SO 4 ) 2 , and buffer E. The reactions were initiated with 1 mM L-cysteine at room temperature. The formation of [2Fe-2S] clusters was monitored by the change in ellipticity at 330 nm (22). The initial increase in ellipticity was plotted with time and fit to a linear equation (R 2 values Ն 0.97) using Kaleidagraph. A 1.50 M/mdeg (see Fig. S2) factor was used to convert ellipticity at 330 nm to [2Fe-2S]-ISCU2 concentration.

[2Fe-2S] cluster transfer reactions from enzymatic reconstituted ISCU2 to GRX5
Clusters were enzymatically generated on ISCU2 (or ISCU2 M140I ) using 0.5 M SDA ec , 20 M ISCU2 (or ISCU2 M140I ), and 400 M Fe(NH 4 ) 2 (SO 4 ) 2 and buffer E. The reactions were initiated with of 100 M L-cysteine and 10 mM GSH at room temperature. After 160 min, the enzymatic formation of [2Fe-2S] clusters appeared to be complete based on the lack of changes in ellipticity at 450 nm. A solution containing 40 M GRX5 (with or without 20 M FXN) was then injected with an air-tight syringe into the sealed cuvette to initiate the transfer reactions. The change in ellipticity was plotted with time and fit to a linear equation with Kaleidagraph (R 2 values Ն 0.97). A 3.77 M/mdeg (see Fig. S2) factor was used to convert ellipticity at 450 nm to [2Fe-2S]-GRX5 concentration.

[2Fe-2S] cluster transfer reactions from holo-GRX5 to apo-ISCU2/ISCU2 M140I
Reactions (200 l) were initiated in an anaerobic cuvette by mixing a final concentration of 20 M [2Fe-2S]-GRX5 with 50 M ISCU2 (or ISCU2 M140I ) in buffer C in the presence and absence of 10 mM GSH. The cuvette was sealed with a rubber septum in an anaerobic glovebox (O 2 Ͻ 0.5 ppm). The cluster transfer reaction was tracked at room temperature by monitoring the spectrum from 300 to 600 nm with time.

Chemical reconstitution of proteins
[2Fe-2S] clusters were chemically generated on ISCU2 (or ISCU2 M140I ) by reacting 30 M (final concentrations) of apo protein in buffer C with 600 M ferric ammonium citrate, 600 M Na 2 S and 10 mM D,L-DTT for 1 h at room temperature. The DTT and the excess iron and sulfide were then removed with a desalting column (5 ml, GE Healthcare) equilibrated in buffer C. The iron concentration was quantitated with the ferrozine assay (extinction coefficient of 28,000 mM Ϫ1 cm Ϫ1 at 562 nm) (41), and sulfide was quantitated using a methylene blue assay with an additional pretreatment of the protein with NaOH and zinc acetate to release bound sulfide (42). The protein concentration was determined using the Bradford assay. Chemically reconstituted ISCU2 had 2.1 Ϯ 0.3 iron and 2.0 Ϯ 0.6 sulfide atoms per protein, whereas ISCU2 M140I had 1.9 Ϯ 0.5 iron and 2.2 Ϯ 0.1 sulfide atoms per protein.

SYPRO-Orange assay for thermal stability analysis of proteins
The samples were prepared anaerobically in a glovebox by mixing 5 l of a 1 mM SYPRO orange (Thermo Fisher) stock solution in water with 5 M (final concentration) of ISCU2 or ISCU2 M140I (with or without chemically reconstituted [2Fe-2S] cluster) in a 20 l (final volume) reaction in buffer C (50 mM HEPES, 250 mM NaCl, pH 7.5). The samples were first equilibrated at 25°C for 5 min, and then the temperature was gradually increased to 100°C in 75 cycles (1°C increase per cycle with a 1-min waiting period) using a quantitative PCR instrument (Stratagene Mx3005P, Agilent Technologies), and the change in fluorescence ( ex , 491 nm; em , 610 nm) was monitored. The raw data were analyzed and fluorescence versus temperature plots were generated using MxPro-Mx3005P software. Melting temperatures were calculated from the peak value of the first derivative plot. All the species had a melting temperature (T m ) of 50 Ϯ 2°C.

[2Fe-2S] cluster extrusion assay
[2Fe-2S] clusters were assembled on 30 M ISCU2 (or ISCU2 M140I ) in the presence of 10 M SDA ec , 100 M L-cysteine, 400 M Fe(NH 4 ) 2 (SO 4 ) 2 , and 10 mM GSH in buffer C. 4 mM D,L-DTT was added to the samples to initiate the cluster extrusion reaction, which was followed by the loss of ellipticity at 330 nm. The extrusion rates were determined by fits to a linear equation.