Cross-linking Evidence for Multiple Interactions of the PsbP and PsbQ Proteins in a Higher Plant Photosystem II Supercomplex*

Background: PsbP and PsbQ are extrinsic subunits of photosystem II (PSII). Results: Using chemical cross-linking, multiple interactions of PsbP and PsbQ with PSII intrinsic subunits, as well as a light-harvesting protein, were detected. Conclusion: Binding of PsbP and PsbQ affects the quaternary structure of the PSII supercomplex. Significance: Our data provide new insights into the organization of PSII extrinsic subunits in higher plants. The extrinsic subunits of membrane-bound photosystem II (PSII) maintain an essential role in optimizing the water-splitting reaction of the oxygen-evolving complex (OEC), even though they have undergone drastic change during the evolution of oxyphototrophs from symbiotic cyanobacteria to chloroplasts. Two specific extrinsic proteins, PsbP and PsbQ, bind to the lumenal surface of PSII in green plants and maintain OEC conformation and stabilize overall enzymatic function; however, their precise location has not been fully resolved. In this study, PSII-enriched membranes, isolated from spinach, were subjected to chemical cross-linking combined with release-reconstitution experiments. We observed direct interactions between PsbP and PsbE, as well as with PsbR. Intriguingly, PsbP and PsbQ were further linked to the CP26 and CP43 light-harvesting proteins. In addition, two cross-linked sites, between PsbP and PsbR, and that of PsbP and CP26, were identified by tandem mass spectrometry. These data were used to estimate the binding topology and location of PsbP, and the putative positioning of PsbQ and PsbR on the lumenal surface of the PSII. Our model gives new insights into the organization of PSII extrinsic subunits in higher plants and their function in stabilizing the OEC of the PSII supercomplex.

The extrinsic subunits of membrane-bound photosystem II (PSII) maintain an essential role in optimizing the water-splitting reaction of the oxygen-evolving complex (OEC), even though they have undergone drastic change during the evolution of oxyphototrophs from symbiotic cyanobacteria to chloroplasts. Two specific extrinsic proteins, PsbP and PsbQ, bind to the lumenal surface of PSII in green plants and maintain OEC conformation and stabilize overall enzymatic function; however, their precise location has not been fully resolved. In this study, PSIIenriched membranes, isolated from spinach, were subjected to chemical cross-linking combined with release-reconstitution experiments. We observed direct interactions between PsbP and PsbE, as well as with PsbR. Intriguingly, PsbP and PsbQ were further linked to the CP26 and CP43 light-harvesting proteins. In addition, two cross-linked sites, between PsbP and PsbR, and that of PsbP and CP26, were identified by tandem mass spectrometry. These data were used to estimate the binding topology and location of PsbP, and the putative positioning of PsbQ and PsbR on the lumenal surface of the PSII. Our model gives new insights into the organization of PSII extrinsic subunits in higher plants and their function in stabilizing the OEC of the PSII supercomplex.
Photosystem II (PSII) 3 is a water-plastoquinone oxidoreductase, driven by light energy, consisting of both membrane-intrinsic and membrane-extrinsic subunits (1). On the thylakoid lumenal side of PSII, the Mn 4 CaO 5 cluster catalyzes water oxi-dation, leading to the production of molecular oxygen, essential for most living organisms on Earth (2). The membrane-intrinsic subunits of PSII are involved in pigment and/or cofactor binding for photochemical reactions, whereas the membraneextrinsic subunits on the lumenal side play crucial roles in stabilizing the Mn 4 CaO 5 cluster and in retaining Ca 2ϩ and Cl Ϫ , required cofactors for water oxidation (3). X-ray structural analysis of the cyanobacterial PSII complex has revealed the organization of its subunits to a resolution of 1.9 Å (4). This crystallographic information, derived from prokaryotic cyanobacterial PSII, cannot necessarily be applied in the context of eukaryotes, due to differences in PSII subunit composition and light harvesting strategies.
It is known that the composition of the extrinsic subunits of PSII has undergone much evolutionary change. Green plant eukaryotes, such as higher plants, green algae, and euglena, have a set of three extrinsic proteins, PsbO, PsbP, and PsbQ, binding to the lumenal surface of PSII. Of note, cyanobacteria have PsbV and PsbU binding to this lumenal surface instead of PsbP and PsbQ, although none of these proteins share any sequence similarity with each other (5,6). In cyanobacteria, there are also homologs of PsbP and PsbQ, termed CyanoP and CyanoQ, respectively (7,8), but these have not yet been included in current structural models. Red algae and diatoms have their own specific lumenally bound extrinsic subunits, such as PsbQЈ and Psb31 (9,10). Interestingly, the PsbP and PsbQ proteins in green plants seem to have evolved from CyanoP and CyanoQ in cyanobacteria, although considerable genetic and functional modifications have occurred to generate the forms of these proteins seen in eukaryotes today (11). The high resolution structures of isolated PsbP and PsbQ proteins have been reported (12)(13)(14)(15). Furthermore, their locations and binding topologies in the green plant PSII complex have been proposed (16,17), but these have not been confirmed experimentally.
The main purpose of PsbP and PsbQ is to optimize the availability of Ca 2ϩ and Cl Ϫ cofactors for efficient water oxidation by PSII. It is reported that the N-terminal region of PsbP spe-cifically interacts with PSII to induce conformational changes around the Mn 4 CaO 5 cluster, required for Ca 2ϩ and Cl Ϫ (18), and PsbQ supports this PsbP function (19). Other recent studies in higher plants suggest that the PsbP and PsbQ proteins are required for stable association of intramembranous light-harvesting proteins (LHCs) with PSII (20,21); however, it remains unclear how the binding of extrinsic subunits of PSII affect the association of LHCs to PSII.
In our study, the interaction of PsbP and PsbQ within the PSII complex was investigated using a chemical zero-length cross-linker, a water-soluble carbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC). We found that PsbP can directly interact with the membrane-intrinsic protein, PsbE, and also with PsbR, a protein we suggest is mostly membrane-extrinsic; in addition, both PsbP and PsbQ interact with the CP26 and CP43 light-harvesting proteins of the LHCII-PSII supercomplex. It is proposed that the above, as a whole, provides a structural basis for the stabilization of the LHCII-PSII supercomplex in higher plants.

Plasmid Construction, Recombinant Protein Expression, and
Purification-The recombinant PsbP_A186C, in which Ala-186 is substituted with Cys, was produced as reported previously (22). To produce the expression plasmid for PsbQ_ G149C, in which Gly-149 is substituted with Cys, cDNA fragments of spinach PsbQ were amplified by PCR with the primers (5Ј-CATATGAGGCCAGGCCCATCGTTGT-3Ј and 5Ј-GAGCTCTTAACAGAGCTTGGCAAGAAC-3Ј) using 30 cycles of 94°C for 30 s, 55°C for 30 s, and 68°C for 30 s. The amplified fragment was purified, digested with NdeI and SacI, and subcloned into the pET 41-a vector (Novagen). The recombinant PsbQ_G149C was expressed in the Escherichia coli strain BL21 (DE3) and purified as described previously (19). The N-terminal Glu-1 of mature PsbQ was truncated during the preparation process. PsbP_A186C and PsbQ_G149C were labeled with maleimide-PEG2-biotin (Pierce) according to the manufacturer's protocol. The presence of the desired mutation in each recombinant protein and in the maleimide-PEG2-biotin labeling was confirmed by MALDI-TOF mass spectrometry (Autoflex III, Bruker).
Reconstitution of the PsbP Protein to NaCl-washed PSII and Cross-linking Experiments-Oxygen-evolving PSII membranes of spinach were prepared as reported previously (23). The activity of isolated PSII membranes was ϳ480 mol of O 2 /mg of Chl/h in the activity measurement buffer (25 mM Mes-NaOH, pH 6.5, 2 M betaine, 20 mM NaCl, 0.4 mM 2,6-dichlorobenzoquinone). The PSII membranes were treated with the high salt buffer (25 mM Mes-NaOH, pH 6.5, 2 M NaCl) to remove the extrinsic PsbP and PsbQ proteins. After incubation for 30 min on ice in the dark, the membranes were sedimented, washed once with buffer (20 mM Mes-NaOH, pH 6.5, 10 mM NaCl), and then resuspended in cross-linking buffer (25 mM Hepes-NaOH, pH 7.2, 25 mM CaCl 2 ). The NaCl-washed PSII membranes, at a concentration of 0.5 mg Chl/ml, were cross-linked with the recombinant biotin-labeled PsbP and/or PsbQ proteins in the cross-linking buffer, including 6.25 mM EDC and 5 mM N-hydroxysulfosuccinimide (sulfo-NHS). The solution was incu-bated for 2 h in darkness, and the reaction was terminated by adding ammonium acetate, to a final concentration of 0.2 M. The solution was centrifuged for 5 min at 20,400 ϫ g at 4°C, and the pellet was subjected to further affinity purification.
Immunoblot Analysis-Proteins separated by SDS-PAGE were transferred to PVDF membranes and analyzed by immunoblotting using specific antibodies. Rabbit antibodies against PsbP and D1 were prepared by the authors. The rabbit antibody against PsbQ was provided by the late Dr. A. Watanabe of Tokyo University. A rabbit antibody against CP43 was a gift from Dr. Y. Kashino of the University of Hyogo. Rabbit antibodies against PsbR, PsbE, and CP26 were purchased from Agrisera AB, Sweden.
Mass Spectrometric (MS) Analysis-The purified proteins were separated by SDS-PAGE and subjected to in-gel digestion with MS-grade modified trypsin (Promega). The peptides were extracted and loaded onto a column (100 m internal diameter, 15 cm length; L-Column, CERI) using a Paradigm MS4 HPLC pump (Michrom BioResources) and an HTC-PAL autosampler (CTC Analytics). Buffers were as follows: A, 0.1% (v/v) acetic acid and 5% (v/v) acetonitrile in water and 0.1% (v/v) acetic acid; and B, 90% (v/v) acetonitrile in water. A linear gradient of buffer B from 5 to 45% was employed, and peptides eluted for 26 min from the column were introduced directly into an LTQ-Orbitrap XL mass spectrometer (Thermo Fisher Scientific) with a flow rate of 500 nl min Ϫ1 and a spray voltage of 2.0 kV. The range of the mass spectrometric scan was a mass-to-charge ratio of 450 to 1500, and the top three peaks were subjected to tandem mass spectrometry analysis.
Search for Cross-linked Sites-Collected data were analyzed using Mass Matrix version 2.4.2 (24). Mass Matrix adopts a staged search strategy. In the first stage, the tandem mass spectrometric data set was searched against the UniProt database using the target-decoy search strategy for protein identification. Reversed sequences were used as a decoy, and the data were filtrated with a Յ1% false discovery rate. In the second stage, protein matches selected from the first stage were searched with the search algorithm that Mass Matrix employs to identify the cross-linked peptides (25). The quality of peptide match was evaluated by three validated statistical measures as follows: pp, probabilistic score based on number of matched peaks; pp 2, probabilistic score based on ion intensity distribution of matched peaks; pp tag , probabilistic score based on consecutiveness of matched peaks. A peptide match with maximum (pp and pp 2 ) Ͼ4.1 and pp tag Ͼ3 was considered to be significant with a p value of Ͻ0.001. The settings of Mass Matrix were as follows: enzyme, trypsin, no Pro rule; decoy database, reversed; missed cleavages, 4; variable modifications, oxidation of Met, His, and Trp, amidation of Asp and Glu, carbamidomethyl of Cys; precursor ion tolerance, 10 ppm; product ion tolerance, 0.8 Da; maximum number of post-translational modification per peptide, 2; mass type, monoisotopic; minimum peptide length, 5; maximum peptide length, 40; crosslink, EDC; cross-link mode, exploratory; cross-link site cleavability, noncleavable by enzyme or not applicable; maximum number of cross-links per peptide, 2.
Structural Modeling-Atomic coordinates from the Protein Data Bank (PDB) of the Research Collaboratory for Structural Bioinformatics were downloaded for the protein subunits or complexes of cyanobacterial PSII (PDB ID 3ARC), higher plant LHCII (PDB ID 2BHW), CP29 (PDB ID 3PL9), PsbP (PDB ID 1V2B), and PsbQ (PDB ID 1NZE). For subunits not yet present in the PDB, spinach sequences for PsbR, CP26, and CP24 were subjected to I-TASSER homology modeling analysis, and in each case the top-scoring model, model1.pdb, was preferred. The most highly ranked protein with a highly similar structure in the PDB, as identified by the TM-align algorithm within I-TASSER, was PDB ID 1V34_A2, PDB ID 2BHW_C, and PDB ID 2BHW_A, respectively, for PsbR, CP26, and CP24. UCSF Chimera (26) was the program used to form the modeling environment, and all subunits were fitted, as surface-rendered rigid bodies, by visual inspection. First, PDB files for the PSII dimer, LHCII trimers, and CP29 subunits were modeled within a molecular envelope derived from a transmission electron microscopy (TEM) as detailed previously (27). This was followed by the substitution of CP26 and CP24 homology models of I-TASSER, in place of previously modeled subunits based upon monomeric LHCII (27). Next, the PDB files for PsbP and PsbQ structures were overlaid across the lumenal surface, taking into account the data from cross-linked sites reported in this study, and finally, the I-TASSER homology model for PsbR was introduced.

Interaction of the PsbP and PsbQ Proteins with LHCII-PSII
Supercomplex Membrane-intrinsic Subunits-Previous studies using EDC hardly detected the cross-linking between PsbP/Q and PSII intrinsic subunits in higher plants. In this study, we combined the conventional release-reconstitution experiment with a chemical cross-linking, followed by affinity chromatography. NaCl-washed PSII membranes were treated with EDC in the presence or absence of biotinylated PsbP or PsbQ. It was confirmed that treatment by 6.25 mM EDC and 5 mM sulfo-NHS did not affect the reconstituted activity of PSII. After purification using Strep-Tactin Sepharose, cross-linked peptides were analyzed by SDS-PAGE, and the bands specifically observed in the presence of biotinylated proteins were used for MS analysis.
As shown in Fig. 1, four cross-linked bands were reproducibly purified by affinity chromatography with biotinylated-PsbP or -PsbQ (P-1 to P-4 and Q-1 to Q-4). The corresponding bands in the SDS-polyacrylamide gels were excised and subjected to in-gel digestion with trypsin. The MS analyses indicated that the bands P-1 to P-4 contained CP43, CP26, PsbR, and PsbE in addition to PsbP, respectively (Table 1 and supplemental Tables S1-S4). The band P-4 corresponds to the cross-linked peptide between PsbP and PsbE that we reported recently (22). Molecular masses of P-1 to P-4 (about 60, 46, 33, and 30 kDa, respectively) indicate that those subunits were cross-linked in a one-to-one (1:1) manner. Similarly, the bands Q-3 (55 kDa) and Q-4 (41 kDa) contained CP43 and CP26 in addition to PsbQ, respectively (Table 1 and supplemental Tables S5 and S6). The bands Q-1 (77 kDa) and Q-2 (65 kDa) also contained CP26 in addition to PsbQ, although their molecular masses indicate that additional subunits should be included; however, they could not be identified due to low database search scores.
The results of the MS analysis on the cross-linked peptides were supported by immunoblot analysis using specific antibodies (Fig. 2, A and B). Bands P-1 to P-4 reacted positively with anti-PsbP antibodies and also with the antibodies specific to CP43, CP26, PsbR, and PsbE. Bands Q-1, Q-2, and Q-4 clearly reacted with antibodies raised against CP26, whereas Q-3 specifically reacted with the anti-CP43 antibodies. It is reasonable  to assume that PsbP has a direct interaction with PsbR, because PsbR is required for the stable binding of PsbP and PsbQ in Arabidopsis (28,29). It is also likely that PsbP and PsbQ can interact with both CP43 and CP26, given the report that CP26 is located close to CP43 in the LHCII-PSII supercomplex (30). Our results are highly consistent with the report demonstrating that PsbQ binding requires the peripheral antenna system, at least the domain that is composed of CP26/LHCII-S (30).

Cross-linked Residues between PsbP and PsbR, and
PsbP and CP26-To identify the cross-linked sites within purified crosslinked peptides, tandem MS/MS spectra were analyzed by the Mass Matrix search engine (24). Possible cross-linking sites between the amino acids Asp to Lys, Glu to Lys, Asp to Ala-1, and Glu to Ala-1 were examined. As a result, cross-linked peptides were identified in the bands P-2 (PsbP and CP26), P-3 (PsbP and PsbR), and P-4 (PsbP and PsbE), although the crosslinked site within other purified peptides could not be identified in this analysis. Fig. 3A shows the tandem MS/MS spectrum of the cross-linked peptide, including RDGVDSSGRKPTGK-GVY 37 from PsbR and KL 28 from PsbP, in which the Asp-22 residue in PsbR and Lys-27 in PsbP were cross-linked. Comparatively, Fig. 3B shows the spectrum of ESSTPVVDGKQYY 127 and FKGAKKF 175 from PsbP and GANCGPEAVW 99 from CP26, in which the Glu-96 in CP26 and the Lys-174 in PsbP were cross-linked. The cross-linking between Ala-1 in PsbP and Glu-57 in PsbE was also detected in P-4, as reported previously (22). The scores of those peptides were statistically significant (p Ͻ 0.001, supplemental Tables S7 and S8), and the amino acid residues identified as cross-linked sites are highly conserved in their respective proteins in higher plants.
The Lys-27 and Lys-174 residues are included in the six domains on the PsbP protein (Lys-11 to Lys-14, Lys-27 to Lys-38, Lys-40, Lys-90 to Lys-96, Lys-143 to Lys-152, and Lys-166 to Lys-174), the modification of which with N-succinimidyl propionate (NSP), which reacts with positively charged amino groups, decreases the binding of PsbP to PSII (31). Also, we recently found that the basic surface on PsbP consisting of conserved Arg-48, Lys-143, and Lys-160 is crucial for the electrostatic interaction with PSII (32). The above information allows us to estimate the binding topology of PsbP to PSII (Fig. 4). The Lys-27 and Lys-174 residues are located on the opposite side of the basic surface of the PsbP structure, indicating that PsbP has multiple interacting surfaces and may function as a link between membrane subunits. The fact that Lys-27 and Lys-174 interact with PsbR and CP26, both peripherally attached to the PSII core complex, suggests that a basic pocket, composed of Arg-48, Lys-143, and Lys-160, would interact with the inner surface of CP43, which is cross-linked with PsbP by EDC ( Figs.  1 and 2). However, the residues closest to its N terminus of PsbP would extend toward cytochrome b 559 (PsbE), around which PsbF, PsbJ, and most likely PsbR as well would make up a subdomain required for the stable binding of PsbP to PSII.
Localization of PsbP and PsbQ within a Higher Plant LHCII-PSII Supercomplex-To further investigate the location of PsbP in the complex, its structure (PDB ID 1V2B) was fitted (Fig. 5) into a TEM-based structural model of negatively stained C 2 S 2 M 2 LHCII-PSII supercomplex samples (27). PsbP was also tentatively positioned close to the lumenal surface of CP43, consistent with a previous report of a three-dimensional reconstruction of a PSII supercomplex from spinach, derived from unstained cryo-TEM samples, calculated by angular reconstitution single-particle analysis (16). Note that the structure of the cyanobacterial PSII core dimer (PDB ID 3ARC) was used, as no eukaryotic PSII structure has been resolved to date; however, the extrinsic subunits PsbU and PsbV, not present in green plants, were removed. Also tentatively placed in our model are PsbQ and PsbR, although their exact binding topology has yet to be directly visualized by microscopy or crystallographic techniques. Furthermore, three-dimensional homology models of spinach PsbR (UniProt/SwissProt accession number P10690), CP26 (GenBank TM accession number AB908271), and CP24 (UniProt/SwissProt accession number P36494) were calculated using the program I-TASSER, and its model1.pdb output was used in all cases (see under "Experimental Procedures"). Of interest, it was found that the structures predicted for CP26 and FIGURE 2. Immunodetection of affinity-purified cross-linked products. The affinity-purified cross-linked peptides using biotinylated PsbP (A) or PsbQ (B) corresponding to 2 g of Chl were separated by SDS-PAGE and immunodetected with antisera against CP43, CP26, PsbP, PsbR, and PsbE, or PsbQ, as indicated on each lane. Arrows indicate the protein bands corresponding to P-1, P-2, P-3, P-4, Q-3 and Q-4, respectively.
CP24 were more closely aligned to that of pea LHCII (PDB ID 2BHW) and its chains C and A, respectively, rather than the recent structure of spinach CP29 (PDB ID 3PL9).
As discussed above, the main structure of PsbP was localized as straddling over the lumenally exposed surface of CP43, where a basic surface consisting of residues Arg-48, Lys-143, and Lys-160 faces toward the extrinsic loop of CP43, although another domain of PsbP, whose surface includes Lys-174, faces outward to CP26 (Fig. 5A). The cross-link between PsbP and CP26 is particularly novel, whereas direct interaction with major LHCs was not suggested by our analysis. In our model, PsbP together with PsbO stabilize the extrinsic loop of CP43 on either side, leading to the optimization of the microenvironment required for the oxygen-evolving center and efficient water-splitting activity (Fig. 5, A, D, and F). Without PsbO, the extrinsic loop of CP43 was likely to be highly flexible. This may explain why PsbP requires PsbO to bind to PSII, although no direct interaction has been detected between them (33), with the extrinsic loop of CP43 acting as a central pillar between them.
PsbP was observed to interact with PsbR, a polypeptide specific to PSII in green plants. The location of PsbR in PSII is predicted to be close to both PsbE and PsbJ (28). The structural model of PsbR predicted by I-TASSER shows a pronounced hydrophobic wedge shape that has been proposed to anchor it to the thylakoid membrane (34). This wedge shape in our study fits well into the gap formed between PsbP and the extrinsic portion of PsbE (Fig. 5B). In this way, the region, including the Lys-27 residue of PsbP, faces toward Asp-22 in PsbR, and the N-terminal 15-amino acid extension of PsbP, unfortunately missing in known x-ray structures, could still reach over to the contact point on the PsbE C terminus (Fig. 5A), an assumption consistent with our cross-linking results.
PsbQ was fitted within a pronounced pocket, observed between PsbP, CP43, and the lumenal membrane surface of the strongly bound LHCII-S trimer (Fig. 5, A and B) (PDB ID 2BHW), oriented to accommodate those previous studies that have suggested its multiple lysine residues (Lys-90, -96, -101, and -102) to be involved in interactions with other PSII components (35). Our results suggest that these particular residues of PsbQ interact with CP43 or CP26, or with PsbP, to stabilize the functional association of PsbP with PSII (19). Such a binding site of PsbQ is surprisingly different from that proposed for CyanoQ in PSII from Synechocystis 6803, as suggested recently by a separate chemical cross-linking study (36). It is therefore likely that the binding site(s) of PsbQ homologs have undergone significant changes during evolution, perhaps manifested in the limited sequence identity between the PsbQ and CyanoQ protein families.

DISCUSSION
In this study, we suggest the direct interaction of PsbP and PsbQ with the membrane-intrinsic PSII subunits, providing additional data for modifying current models of the organization of lumenally bound extrinsic subunits in higher plant PSII.
It has been widely believed that once PsbO directly binds to the PSII core, PsbP binds to PsbO, and then PsbQ binds to PsbP or PsbO (33). However, several reports suggest that PsbO can be extracted without affecting PsbP and PsbQ binding, thereby indicating that PsbP and PsbQ directly associate with the PSII intrinsic subunits (37)(38)(39). Indeed, in our MS analysis, none of the bands P-1 to P-4 includes PsbO peptides nor Q-1 to Q-4 PsbO and PsbP. We do not exclude the possibility of there being a direct interaction between extrinsic subunits in higher plants PSII. In fact, it is reported that an EDC cross-linked product formed between PsbP and PsbQ in the green alga Chlamydomonas (40).
A direct interaction of PsbP with both PsbE and CP43 indicates that PsbP occupies a position roughly similar to that occupied by PsbV in the cyanobacterial crystal structure, in which the N terminus of PsbV (Ala-1) forms a charge-pair interaction with Asp-53 in PsbE, and the C-terminal main structure is associated with the CP43 protein (4). PsbV is suggested to have a function similar to PsbP regarding ion retention; hence, it may be reasonable to assume that its structural interactions are also similar. Given genetic studies using Arabidopsis report that knockdown of PsbP expression correlates with a loss in PsbQ, D2, and CP47 accumulation (41), PsbP being localized next to CP43 would also affect the stability of the further D2/CP47 side of each PSII monomer, probably through interaction with PsbR and also with PsbE via its N-terminal sequence.
It is probable that PsbP, PsbQ, and PsbR in higher plant PSII may all play significant roles, most likely via a defined temporal sequence, in providing enhanced structural rigidity for CP43 against PsbO. This rigidity could then be transmitted down into the membrane, locking in the protein scaffold and the ligands surrounding the Mn 4 CaO 5 cluster of the oxygen-evolving center, thereby optimizing enzymatic activity. A further interesting observation to be noted is that a substantial part of the PsbO subunit, of one PSII monomer, reaches over to the CP47 extrinsic loop of the second monomer (Fig. 5A, white arrows) in the overall PSII dimer (PDB ID 3ARC). The binding of PsbP, PsbQ, and PsbR, via CP43 and its extrinsic loop, may make PsbO rigid enough to even stabilize the CP47 extrinsic loop of the second monomer, across the dimeric symmetry, further stabilizing the whole dimeric complex.
Our results also indicate that PsbP, together with PsbQ, can be structurally linked in stabilizing the association of a minor antenna protein, CP26, to the inner membrane-facing domains of CP43. This, in turn, will be relevant to the significance of these extrinsic subunits for the overall supramolecular organization of PSII (20,30,42) and their influence on the rate of state transitions (21). A major problem for our model is Lys-174 of PsbP. This is located about 35-37 Å away from its expected CP26 cross-linked site Glu-96 (Fig. 5, A and E). The 15-amino acid extension of PsbP, currently unresolved in the literature (see above), might eventually allow for some shifting of the PsbP position toward CP26, but still some distance would remain. A possibility remains whereby a secondary binding site exists, to which PsbP may transiently interact, during the PSII assembly process. Indeed, previous studies have suggested that two PsbP per PSII are required for the full activation of the oxygen-evolving activity (43), and truncation of nine N-terminal residues of  (4), based upon comparisons with the literature (27,30). Putative PsbP-binding sites are indicated by light yellow circular overlays. PsbV and PsbU, known to be absent in plant PSII, were excluded. CP43 and PsbE, which interact with PsbP, are shown in light blue and red, respectively. PsbJ and PsbO, required for the stable binding of PsbP and PsbQ, are shown in orange (indicated by arrows) and purple, respectively. Positioning of the strongly (S) or moderately (M) bound LHC trimers, as well as the minor LHC antennae CP24 (24), CP26 (26), and CP29 (29), are schematically depicted. CP26 is outlined in magenta to indicate its interaction with PsbP and PsbQ.
PsbP increase the amount of PsbP bound to PSII in the reconstitution experiments using salt-washed PSII membranes (44).
In conclusion, we have shown that PsbP and PsbQ are capable of multiple interactions with PSII intrinsic subunits as well as other light-harvesting proteins present within the larger, stable PSII supercomplex form. This indicates that PsbP and PsbQ not only replace the function of PsbU and PsbV structurally but have evolved the ability to stabilize the overall LHCII-PSII supercomplex in green plants. It is plausible that an evolutionary change of the PSII extrinsic proteins, to increase the efficiency of maintaining the water-splitting microenvironment in higher plants, might be related to the modification in the outlying PSII light-harvesting antenna system, including the subunit CP26. Because the association of the peripheral antennae to PSII is a dynamic process, these lumenally bound, extrinsic PsbP and PsbQ proteins are likely to also have a direct role in adjusting the photosynthetic light reactions to rapidly changing environmental conditions. It is clear that high resolution (Ͼ10 Å resolution) direct structural analysis, by crystallography or three-dimensional cryo-TEM, is required to reveal the detailed extrinsic lumenal relationships between PsbP, PsbQ, CP26, PsbR, and PsbO, the extrinsic loops of CP43 and CP47, and the whole LHCII-PSII supercomplex. Protein coordinates (see text for PDB IDs) are shown either as schematic ribbons or transparent space-filling spheres as follows: PsbP (green), PsbQ (yellow), CP43 (light blue), PsbO (purple), PsbR (cyan), PsbE (red), CP26 (magenta), LHCII-S (light gray), and CP47 (white). A, top view, looking down onto the membrane plane from the lumen. Subunit labels are in white. Key amino acid residues of cross-linked sites are shown as blue spheres, and labels are color-coded as per associated proteins. Position of the Mn 4 CaO 5 cluster (Mn cluster) is circled in black; manganese atoms are small red spheres and calcium atoms are orange. The PsbO protein of each PSII core monomer has a distinct feature that extends over to the adjacent PSII monomer, here noted by a white star and emphasized with a split arrow. B, slab (cut-away) view of A. PsbJ is highlighted in orange, due to it being mostly hidden in A. The 2-fold symmetry of the overall PSII dimeric core is emphasized by dashed line. C, side view of A. The thickness of the slab in B (ϳ1.2 nm) is marked with * and shown with dashed lines. D, slab of the entire lumenally protruding protein domain shown in schematic ribbon form, emphasizing the cross-links between key residues of PsbP, PsbQ, PsbR, and PsbE; note this is also in the same orientation as A and B. The extent of E and F slabs is also shown. E, slabbed side view of C, emphasizing all cross-link site key residues. The depth of this slab is shown in D. F, end view of E and C, slabbed from the tip of LHCII-S to PsbE. The depth (ϳ5 nm) of D slab is also shown. Scale bar, 2 nm (for all panels).