Plastoquinone (PLQ) acts as an electron carrier between photosystem II (PSII) and the cytochrome b6f complex. To understand how PLQ enters and leaves PSII, here we show results of coarse grained molecular dynamics simulations of PSII embedded in the thylakoid membrane, covering a total simulation time of more than 0.5 ms. The long time scale allows the observation of many spontaneous entries of PLQ into PSII, and the unbinding of plastoquinol (PLQol) from the complex. In addition to the two known channels, we observe a third channel for PLQ/PLQol diffusion between the thylakoid membrane and the PLQ binding sites. Our simulations point to a promiscuous diffusion mechanism in which all three channels function as entry and exit channels. The exchange cavity serves as a PLQ reservoir. Our simulations provide a direct view on the exchange of electron carriers, a key step of the photosynthesis machinery.
Photosynthetic organisms convert light into chemical energy. This fundamental process involves four major protein complexes: photosystem II (PSII), cytochrome b6f complex (Cyt b6f), photosystem I and ATP synthase1,2. The process starts at PSII, which extracts electrons from water. The electrons travel subsequently to Cyt b6f and PSI, after which they reduce NADP+. The electrons are transported between these protein complexes by charge carriers. Plastoquinone (PLQ) is the charge carrier responsible for the electron transport from PSII to Cyt b6f. Upon photoactivation of PSII, PLQ is double reduced and takes up two protons to become plastoquinol (PLQol) (Fig. 1a).
The PSII core complex, a homodimer consisting of 27 subunits in plants and 20 in cyanobacteria3,4,5, coordinates two PLQs per monomer, named QA and QB, symmetrically positioned around a non-heme iron (Fig. 1b,c, ). QA is stationary and does not leave the protein; it just passes the electron on to QB. QB, however, leaves the protein after its conversion to PLQol; then a new QB enters the binding site and the process can start again. In the X-ray structure of Guskov et al.3 a third PLQ is present, coined QC. QC is however not found in the later Umena and Wei structures4,5. The QC site is located close to the QB site, but the role of QC is still highly debated.
While the QA site is well buried in the core of the PSII complex, the QB and QC sites connect to a small cavity located within the protein (Fig. 1c). This so-called PLQ/PLQol exchange cavity is filled with lipids: on the stromal side with the negative charged phosphatidylglycerol (PG) and sulfoquinovosyldiacylglycerol (SQDG) lipids and on the lumenal side with digalactosyldiacylglycerol (DGDG) and monogalactosyldiacylglycerol (MGDG) lipids4. Two channels link the cavity to the thylakoid membrane3. Channel I, containing the tail of QC, is flanked by cyt b559α and PsbJ and opens up to the centre of the thylakoid membrane. The QC head group protrudes into the PLQ exchange cavity, where it interacts with lipid and cofactor tails, but not with any amino acids. Channel II, containing the QB tail, is located between the D2 subunit and cyt b559β, opening up more on the stromal side compared to channel I. The QB headgroup is located close to the non-heme iron.
The presence of these two channels led to three different models for PLQ/PLQol diffusion involving the QB and QC sites3. In the ‘alternating’ mechanism, channels I and II are used both as an entry and as an exit. Each PLQol leaves however through the same channel as through which it entered as a PLQ. In the ‘wriggling’ mechanism, PLQ enters via channel I and PLQol leaves via channel II. This would be in line with the fact that PLQol is more polar than PLQ, preferring to leave through channel II which opens up closer to the membrane surface6,7. In the ‘single channel’ mechanism, only channel II is used and channel I is occupied by a stationary PLQ molecule (QC) that might be involved in redox reactions with cyt b559 (refs 8, 9).
Here we present the results of coarse grained (CG) molecular dynamics (MD) simulations of the diffusion of PLQ and PLQol in and out of the cyanobacterial PSII complex. The use of a CG model enables simulations of multi-meric protein assemblies in a complex membrane environment, exploring time scales in the microsecond range10,11,12,13,14. Recently, we described the dynamics of the PSII complex including all of its cofactors, embedded in a realistic description of the thylakoid membrane based on the CG Martini model15. We extended this work, and now focus our analysis on the exchange pathways of PLQ and PLQol by quantifying the role of the different channels. Previous computational work has focused on the energetics of the QA and QB binding sites16, and on simulation of PLQ either in solution16 or in the thylakoid membrane17; for a review see ref. 18. An atomistic simulation has recently been performed on the difference in binding of PLQ/PLQol at the QB site19, but the simulation time was too short to observe any unbinding events. To our knowledge no simulations have been performed to address the full exchange of PLQ/PLQol in and out of PSII, which is the topic of the current manuscript.
We simulated the PSII dimer complex of the cyanobacteria T. vulcanus, including all cofactors and embedded in a realistic representation of the thylakoid membrane composed of MGDG, DGDG, SQDG and PG lipids (Fig. 2). To probe the exit and entry pathways of PLQ and PLQol, the QB site was initially occupied by a PLQol, and PLQs were placed in the bulk membrane at about 5 mol%. Five replicate simulations were performed for a time period between 80 and 100 μs each (see Methods for details). We observe multiple binding and unbinding events of the electron carriers, and discover a new pathway, denoted channel III (Fig. 1c), by which PLQ and PLQol can enter or leave the PSII complex.
PLQol leaves the QB site on a microsecond time scale
In our previous simulations of the PSII dimer we showed that the oxidized form of the electron carrier, PLQ, remains stably bound at the QB site15. We anticipate that the reduced form, PLQol, should leave the binding site in order to deliver two electrons to the cytochrome b6f complex. In line with our expectations, we observe the spontaneous unbinding of PLQol from the QB site. Out of ten PLQols (two per dimer), five of the PLQols leave the QB site completely during the simulation. Out of these five, one PLQol escapes the protein ending up in the bulk thylakoid membrane, two end up in the PLQ exchange cavity, and two remain trapped in the channels. The other five PLQols stay largely in place, with only transient or partial unbinding events being observed (for example, rapid rebinding, or unbinding of the head group but not of the tail). Individual unbinding times vary greatly, from within 0.1 to tens of microseconds, pointing out the stochastic nature of the unbinding process (see Supplementary Fig. 1). Note time scales in CG MD are only approximate; please see the SI for a more detailed discussion on their interpretation.
PLQ enters exchange cavity and reaches binding sites
To investigate how PLQs diffuse into the PLQ exchange cavity, we calculated a PLQ density map, combining the data from the five replicate simulations that contained additional PLQ molecules (138 molecules, ∼5 mol%) in the surrounding bulk thylakoid membrane. The resulting density map is visualized in Fig. 3a, showing the areas around the PSII dimer where it is more likely to encounter a PLQ during the simulation.
The first remarkable feature is the non-homogeneous distribution of PLQ around the protein. PLQ clearly has a preferred region of interacting with PSII, ranging approximately from subunits PsbZ to PsbH, with a few spots around CP43 and D1 where the PLQ tries to penetrate PSII. Remarkably, there is no density in and around the dimer cleft. It appears that PLQs accumulate at the side of the protein with access to the exchange cavity.
The exchange cavity itself is also clearly visible in the density map. This implies that PLQs spontaneously enter the exchange cavity from the bulk thylakoid membrane. Interestingly the density is not homogenously distributed within the cavity, but located more towards the cyt b559 and away from CP43 (Fig. 3a). At the end of the simulation the amount of PLQ inside the exchange cavity is 1.0±.2 (s.e.m., n=10) PLQ molecules. It is likely that this is still an underestimation, as equilibration of the PLQ population in the exchange cavity is a slow process. Note that, in most simulations, a PLQol molecule is also present, either at the QB site or trapped in the exchange cavity.
Despite the presence of PLQ in the exchange cavity we did not observe in any of the simulations PLQ docking into the QB site, which would in principle be possible in the cases in which PLQol has left. This is reflected by the lack of density right at the QB site. The QC site, on the other hand, is frequently visited by PLQs as is apparent from the density map. In addition, the QA site, containing the stationary PLQ molecule, is clearly visible. Visual inspection of the trajectories shows that subtle side chain reorientations, especially of D1-HIS215, that occur after unbinding of PLQol, prevent easy access to the QB binding site. In order to increase the chance of a PLQ binding to the QB site, more than 50 μs of adaptive MD was performed (see Methods). During the adaptive MD simulations PLQ could closely approach the binding position found in the crystal structure, although with a slightly different orientation of the PLQ headgroup (see Supplementary Fig. 2).
Discovery of a third exchange channel
Interestingly, the PLQ density map shows the existence of three clear distinct pathways connecting the membrane to the PLQ exchange cavity, indicated by arrows in Fig. 3a. These pathways correspond to channels I and II previously reported in the literature3, as well as a novel pathway, denoted channel III. Our data thus imply the existence of a third exchange channel. The novel channel emerges when PsbJ moves towards cyt b559α while PsbK and ycf12 move in the opposite direction, creating a tunnel between PsbJ on one side and PsbK and ycf12 on the other side.
To get an estimate about the PLQ fluxes through the three channels we counted how many PLQs pass through each channel in the five different simulations (see Supplementary Methods, Supplementary Table 1). The data are shown in Table 1, averaged over the ten monomers (results for the individual monomers are given in Supplementary Table 2). In total, we observed 19 full entries and 11 full exits, over the 0.5 ms aggregate simulation time. In addition, many additional PLQs are found trapped inside the channels at the end of the simulation.
Our data furthermore show that each of the channels is used both as an entrance and as an exit to the PLQ cavity. Sometimes a different channel is used to leave the cavity than the channel used to enter. It is however also common that the same channel is used. In most of the complexes, the entry flux is higher than the exit flux (Table 1), causing the net increase in the amount of PLQs present in the PLQ exchange cavity (see above). On average, every 33 μs a cofactor enters or leaves one of the two PLQ cavities.
Comparing the fluxes between the channels, it appears that channels I and III are used by PLQ with roughly the same frequency, but significantly fewer cofactors pass through channel II. In the latter channel, they often get stuck and do not completely pass through the channel (see also Supplementary Table 2), which we attribute to the smaller size of channel II. Channel I has dimensions of 1.0 × 2.0 nm2, while the dimensions of channel II are only 1.0 × 1.2 nm2 (ref. 20). We estimate the size of channel III as 1.1 × 2.0 nm2, similar to channel I (see Supplementary Methods). During the simulation, the shape and size of the channels fluctuates significantly, with sizes transiently increasing or decreasing up to 100%.
To explore whether PLQols can also enter the cavity using the same channels, six additional simulations were performed (aggregate time 0.25 ms) with PLQol at 5 mol% in the bulk membrane (see Supplementary Methods). The results (Supplementary Tables 3 and 4) indicate a very similar behaviour as observed for PLQ, implying that PLQol is potentially able to (re)enter the PLQ exchange cavity.
Visual inspection of our simulation trajectories reveals that the subunits lining the channels are dynamic, and can move with respect to each other. In particular, there is movement of the helices cyt b559α+β, PsbJ, PsbK ycf12 and PsbX. These relative movements can either result in constriction or even complete closure of a channel, or result in an increased capacity of a channel due to a larger channel opening. This is especially noticeable for channels I and III. Graphical snapshots illustrating the entrance of PLQ through channel I, the exit of PLQol through channel III and the opening of channel III are shown in Fig. 3b,c. See also Supplementary Movies 1–3.
PLQs can reorient inside the exchange cavity
Also of interest is the observation that both PLQs and PLQols can enter the channels in two orientations, headgroup first or tail first (see Supplementary Fig. 3). Inside the exchange cavity, PLQ can further reorient by flip-flopping between the stromal and lumenal leaflets. We observed 14 such events during the 0.5 ms aggregate time of the five replicate simulations. Taking into account the amount and time PLQ molecules spent inside the cavity, this corresponds to a flip-flop time scale of the order of 100 μs. Compared to the typical flip-flop time of PLQ in the thylakoid bulk membrane, which is around 1 μs as estimated from simulations using the same CG model17, reorientation dynamics inside the cavity is thus slowed down by two orders of magnitude. In case of PLQol, no flip-flop events were observed for the PLQol molecules inside the cavity, in any of the six replicate simulations. Again taking into account the amount and time spent in the cavity, we estimate a lower bound of the reorientation time scale of 200 μs. The lower flip-flop rate of PLQol compared to PLQ is in line with the lower flip-flop rate for PLQol versus PLQ in bulk membranes (at least one order difference17,21), and can be attributed to the more polar nature of the reduced cofactor.
We have investigated the behaviour of PLQ and PLQol in PSII, based on coarse-grained molecular dynamics simulations. The CG approach allowed us to simulate the full PSII dimer system, including all cofactors and embedded in a realistic thylakoid membrane environment, on an aggregate time scale of almost 0.5 ms. We find that PLQs accumulate around the PSII complex at sides close to the exchange cavity, and are able to enter and leave this cavity using three different channels. Of these, two channels correspond to the known channels I and II. The third channel is a novel channel that has not been reported before. Taken together, our simulations point to a plastic behaviour of the PLQ exchange channels. Here we discuss our results in light of the current literature view on PLQ binding and exchange pathways. A discussion of the limitations of our approach can be found in the Supporting Information (Supplementary Note 1). In light of these limitations, it is imperative that our results are eventually verified by more detailed all-atom models, and/or validated experimentally.
In our simulations with PLQ occupying the QB site, both QA and QB remain stationary. This is in line with their function in photosynthesis. Experiments suggests that it is relatively difficult to remove QA from its binding site22,23,24. The QB PLQ is only expected to leave the site after being converted to PLQol. This is confirmed by our simulations: we observe that while all PLQs remain in the QB pocket, PLQols diffuse out of this binding site. The affinity of PLQ and PLQols for the QC site appears weak. Although the site is frequently visited by PLQ/PLQols diffusing through channel I, actual binding is not observed. We hypothesize that the QC site in the crystal structure of Guskov et al.3 either originates from a PLQ trapped inside the channel under the crystallization conditions, or represents a number of weaker binding spots around the QC site.
The simulations reveal that there are preferential regions on PSII where PLQ interacts, and from which PLQ can enter the exchange cavity. Importantly, our data suggest that the PLQ cavity could function as a PLQ reservoir. We quantified a gain of about one PLQ molecule per monomer compared with the Umena structure in which only QB is present4. Considering our simulations did not reach equilibrium yet, the equilibrium population could be even higher. The PLQ exchange cavity can thus function as a kind of local reservoir of PLQs, where PLQs can reorient. The latter is especially relevant because some of the PLQs enter tail first. Note that the PLQ cavity reservoir should not be confused with the total PLQ pool, which is likely located for a large part outside the PSII complex in the thylakoid membrane, and estimated to contain between 9 and 30 PLQs per complex25,26. The entry and exit kinetics of PLQ, on average one PLQ per 33 μs per monomer, is fast compared to both the first reduction step of PLQ at the QB site towards semiplastoquinone, that has a time constant of a few hundreds of microseconds, and the second redox step that shows somewhat slower kinetics26,27. This implies that a PLQ is always available close to the QB site to replace PLQ upon its reduction to PLQol, at least when the PLQ pool is largely oxidized. Interestingly, the simulations with excess PLQol in the thylakoid membrane showed that the reduced electron carrier is able to potentially re-enter the exchange cavity, competing with PLQ. This could be an important regulation mechanism to reduce reduction rates under conditions when PSII is operating too fast and the PLQ pool becomes reduced.
Our simulations provide direct evidence for the existence of designated PLQ/PLQol exchange pathways. Surprisingly, we find exchange taking place via three distinct channels, rather than two channels that are thus far assumed. Apart from channel I and channel II that have been described before3, we observed a third channel between subunits PsbJ and ycf12/PsbK. The simulations show that channels I and III are used more or less equally, but that the narrower channel II is used significantly less. The subunits lining the three channels can undergo conformational changes, modulating the relative opening or closure of channels I and III in particular. Is channel III really used in vivo? Mutants studies have already shown that PsbJ is likely to be involved in the electron transport from QA to the PLQ pool, pointing to the importance of cyt b559 for photosynthesis, and revealed that PsbX has an influence on PLQ turnover28,29,30,31,32,33,34. However, a way to really assess the existence of channel III in vitro could be by measuring the distance between the various helices over time. This could be achieved by the inclusion of fluorescent or electromagnetic probes in helices cyt b559α, PsbJ and ycf12 and subsequently reading out the distances between the subunits over time using FRET or EPR measurements. Closing channels, by crosslinking the constituent helices, might be another approach to study the existence and the usage of the various channels. One might be able to close, for example, channel III by crosslinking PsbJ, ycf12 and PsbK together and subsequently measure the effect on the redox potential of QA and the PLQ pool.
In the literature, three different PLQ exchange mechanisms have been proposed: the alternating, the wriggling and the single channel mechanism3. The simulations do not match any of them fully. Our data agree with the alternating mechanism in the sense that both channels are used as an entry and an exit. It differs to the point that the cofactors do not have to leave through the same channel as through which they entered. Our simulations agree with the wriggling mechanism to the point that channel I can be used for PLQ entry and channel II for PLQol exit. In the wriggling model, however, channel I is exclusively used as an entry and channel II exclusively as an exit. We observe that PLQs enter the PLQ cavity using all channels and that PLQol can leave the binding site also making use of all three channels. Our simulations do not agree with the single channel mechanism in which only channel II is actively used and channel I is occupied by a stationary PLQ. In our simulations, the flux through channel I is actually significantly larger. Our findings are therefore also in disagreement with the conclusions derived from the MD study of Zobnina et al.19, apparently supporting the existence of a single channel model. Our simulations are however four orders of magnitude longer and Zobnina et al.19 do not observe any actual exchange of PLQs or PLQols. Finally, in all three mechanisms the PLQs directly diffuse to the QB site after entering a channel and directly leave the complex after being reduced to PLQol. In contrast, we observe the exchange cavity to serve as a PLQ reservoir allowing for substantial PLQ rearrangements before/after binding/unbinding.
The model emerging from our simulations is one in which three channels exist, each serving as both entry and exit pathway for both PLQ and PLQol. The exchange cavity serves as a temporary PLQ reservoir in which the PLQs can reorient. We denote this model the ‘promiscuous’ mechanism, to be considered as alternative for the alternating, the wriggling and the single channel mechanisms. A schematic of the new model is shown in Fig. 4.
Taken together, based on large-scale simulations, we have been able to shed important light on the mechanism by which PLQs and PLQols can diffuse in and out of the PSII complex. Our simulations do not fully agree with any of the three diffusion mechanisms described in the literature3. Instead they point to a less organized, less deterministic model. Nine main observations can be made. (1) Three different channels exist that all can be used as an entry and an exit channel. (2) The entry and exit channel do not have to be the same for an individual PLQ; a number of PLQs enter and leave through the same channel, but others do this by a different channel. (3) The QC site likely represents a weaker binding spot. (4) PLQs can pass through the channels in at least two different orientations, with their headgroup first or with their tail first. (5) PLQs do not directly dock at the QB site from the channel, instead they first enter in the PLQ exchange cavity where they can diffuse around and reorient themselves. (6) PLQs can accumulate in the PLQ exchange cavity forming a PLQ reservoir. (7) The flux through channels I and III is more or less equal and several times larger than through channel II. (8) The relative flux through channels I and III is influenced by the relative conformations of cyt b559, PsbJ, ycf12 and PsbK. Possibly PsbX might be able to influence the flux through channel II. (9) The side of the protein where the channel openings are located acts as a funnel, accumulating PLQs towards the entrances of the exchange cavity.
The combination of these nine observations leads to a new model, the ‘promiscuous’ mechanism, in which channels I and III are primarily used, and each channel functions as an uncorrelated entry and exit of PLQ/PLQol. The PLQ exchange cavity can function as a local PLQ supply in which the PLQs and PLQols can reorient and there is a regulatory function of subunits cyt b559, PsbJ, ycf12 and PsbK.
To study the dynamics of PLQ and PLQol exchange in the PSII complex, we used the equilibrated structure from our previous simulations of the PSII complex15. Here, we describe five independent simulations of the dimer in which the QB pocket contained a PLQol and extra PLQs were added to the thylakoid membrane.
The simulations are based on the crystal structure of the cyanobacterial PSII complex from Umena et al.4 with PDB ID: 3ARC. The protein was coarse grained together with all of its cofactors and embedded in a thylakoid membrane composed out of 2,686 lipids using the insane script35. The membrane is composed of the negative charged PG and SQDG, and the neutral MGDG and DGDG lipids with oleoyl and palmitoyl tails, a realistic representation of the thylakoid membrane17,36. The system further contains 73,144 CG water beads (representing four times as many water molecules), 455 Na+ and 455 Cl− ions (around 100 mM NaCl), plus 1032 Na+ counter ions to neutralize the overall charge. More details of the setup of this system can be found in our recent publication15.
The five different simulations described in the current work all started from the same initial structure, but with different seeds for the initial randomized velocities. In order to investigate the pathways of PLQ diffusion to the QB binding site, 69 PLQ molecules were inserted into each membrane leaflet at the start of the simulation, totalling to 138 free PLQs, yielding a concentration of about 5 mol % in the membrane. The PLQs were added to a pre-equilibrated bilayer by increasing the lateral dimensions of the box by 1.27 nm and adding 69 PLQs to each leaflet using the insane script35. The PLQs present in the QB sites were modified to PLQols. The QC site was left unoccupied.
The Martini force field version 2.2 (refs 37, 38) in conjunction with the ElNeDyn elastic network39 were used to model the interactions. The PLQ and PLQol parameters originate from ref. 21. The lipid parameters were taken from ref. 40 with the modification as described in ref. 17. GROMACS version 4.5.5 (ref. 41) was used to integrate the equations of motion with the common Martini settings for the Martini force field42. The simulations were run in the isothermal-isobaric (NpT) ensemble. Since T. vulcanus is a thermophile, the simulations were performed at 328 K, maintaining the thylakoid membrane in the fluid phase. The temperature was controlled using the V-rescale thermostat with a coupling constant of τt=2.0 ps (ref. 43). The pressure was semi-isotropically coupled to an external bath of p=1 bar with a coupling constant of τp=1.0 ps and a compressibility of χ=3.0−4 bar−1 using the Berendsen barostat44. A shifted potential with a cutoff of 1.2 nm in conjunction with a dielectric constant of 15 was used to model the electrostatic interactions. The Van der Waals interactions were also calculated using a shifted potential, with a cut off of 1.2 nm and a switch at 0.9 nm.
The five replicate simulations had a length of 84.2, 92.1, 97.4, 94.3 and 106.5 μs, summing up to almost 0.5 ms. Trajectories were saved and analysed every 500 ps, the first 1 μs being discarded as equilibration time. In order to increase the chance of a PLQ docking to the QB site, an adaptive MD simulation approach was used consisting of an iterative process in which new, relative short simulations are spawn from promising configurations. Such an adaptive approach has been shown to be efficient in observing rare events, such as the binding of a ligand to its binding pocket45. Here, configurations were selected in which a PLQ was in a favourable condition to approach the bicarbonate ion. All together, we performed 41 independent short simulations totalling more than 50 μs simulation time. Details of the analysis, and additional simulations with excess PLQol, can be found in the Supporting Information (Supplementary Methods)46,47. Visual molecular dynamics (VMD) (ref. 46) and pymol (ref. 47) were used to generate the images.
The authors declare that all data supporting the findings of this study are available within the manuscript and its supplementary files or are available from the corresponding author on request.
How to cite this article: Van Eerden, F. J. et al. Exchange pathways of plastoquinone and plastoquinol in the photosystem II complex. Nat. Commun. 8, 15214 doi: 10.1038/ncomms15214 (2017).
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Blankenship, R. E. Molecular Mechanisms of Photosynthesis Wiley Blackwell (2014).
Croce, R. & van Amerongen, H. Natural strategies for photosynthetic light harvesting. Nat. Chem. Biol. 10, 492–501 (2014).
Guskov, A. et al. Cyanobacterial photosystem II at 2.9-Å resolution and the role of quinones, lipids, channels and chloride. Nat. Struct. Mol. Biol. 16, 334–342 (2009).
Umena, Y., Kawakami, K., Shen, J.-R. & Kamiya, N. Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9Å. Nature 473, 55–60 (2011).
Wei, X. et al. Structure of spinach photosystem II–LHCII supercomplex at 3.2 Å resolution. Nature 534, 69–74 (2016).
Nowicka, B. & Kruk, J. Occurrence, biosynthesis and function of isoprenoid quinones. BBA—Bioenergetics 1797, 1587–1605 (2010).
Müh, F., Glöckner, C., Hellmich, J. & Zouni, A. Light-induced quinone reduction in photosystem II. Biochim. Biophys. Acta 1817, 44–65 (2012).
Bondarava, N. et al. Evidence that cytochrome b559 mediates the oxidation of reduced plastoquinone in the dark. J. Biol. Chem. 278, 13554–13560 (2003).
Kaminskaya, O., Shuvalov, V. A. & Renger, G. Evidence for a novel quinone-binding site in the photosystem II (PS II) complex that regulates the redox potential of cytochrome b559. Biochemistry 46, 1091–1105 (2007).
Ingólfsson, H. I. et al. Lipid organization of the plasma membrane. J. Am. Chem. Soc. 136, 14554–14559 (2014).
Arnarez, C., Marrink, S. J. & Periole, X. Molecular mechanism of cardiolipin-mediated assembly of respiratory chain supercomplexes. Chem. Sci. 7, 4435–4443 (2016).
Chavent, M., Duncan, A. L. & Sansom, M. S. Molecular dynamics simulations of membrane proteins and their interactions: from nanoscale to mesoscale. Curr. Opin. Struct. Biol. 40, 8–16 (2016).
Koldsø, H. & Sansom, M. S. P. Organization and dynamics of receptor proteins in a plasma membrane. J. Am. Chem. Soc. 137, 14694–14704 (2015).
Holdbrook, D. A., Huber, R. G., Piggot, T. J., Bond, P. J. & Khalid, S. Dynamics of crowded vesicles: local and global responses to membrane composition. PLoS ONE 11, e0156963 (2016).
van Eerden, F. J. et al. Molecular dynamics of photosystem II embedded in the thylakoid membrane. J. Phys. Chem. B 121, 3237–3249 (2017).
Ishikita, H., Hasegawa, K. & Noguchi, T. How does the QB site influence propagate to the QA site in photosystem II? Biochemistry 50, 5436–5442 (2011).
van Eerden, F. J., de Jong, D. H., de Vries, A. H., Wassenaar, T. A. & Marrink, S. J. Characterization of thylakoid lipid membranes from cyanobacteria and higher plants by molecular dynamics simulations. BBA—Biomembranes 1848, 1319–1330 (2015).
Lambreva, M. D. et al. Structure/function/dynamics of photosystem II plastoquinone binding sites. Curr. Protein Pept. Sci. 15, 285–295 (2014).
Zobnina, V. et al. The plastoquinol-plastoquinone exchange mechanism in photosystem II: insight from molecular dynamics simulations. Photosynth. Res. 131, 15–30 (2017).
Kern, J., Zouni, A., Guskov, A. & Krauss, N. in Lipids in Photosynthesis Vol. 30 (eds Wada, H. & Murata, N.) 203–242Springer Netherlands (2009).
de Jong, D. H. et al. Atomistic and coarse grain topologies for the cofactors associated with the photosystem II core complex. J. Phys. Chem. B 119, 7791–7803 (2015).
Ermakova-Gerdes, S. & Vermaas, W. Mobility of the primary electron-accepting plastoquinone QA of photosystem II in a Synechocystis sp. PCC 6803 strain carrying mutations in the D2 protein. Biochemistry 37, 11569–11578 (1998).
Diner, B. A., de Vitry, C. & Popot, J.-L. Quinone exchange in the QA binding site of Photosystem II reaction center core preparations isolated from Chlamydomonas reinhardtii. BBA—Bioenergetics 934, 47–54 (1988).
Araga, C. et al. Functional reconstitution of the primary quinone acceptor, QA, in the Photosystem II core complexes. BBA—Bioenergetics 1142, 36–42 (1993).
Govindjee, G. Chlorophyll a fluorescence: a bit of basics and history Kluwer Academic Publishers (2004).
Kolber, Z. & Falkowski, P. G. Use of active fluorescence to estimate phytoplankton photosynthesis in situ. Limnol. Oceanogr. 38, 1646–1665 (1993).
Kern, J. & Renger, G. Photosystem II: Structure and mechanism of the water:plastoquinone oxidoreductase. Photosynth. Res. 94, 183–202 (2007).
Katoh, H. & Ikeuchi, M. Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus. Plant Cell Physiol. 42, 179–188 (2001).
Lind, L. K., Shukla, V. K., Nyhus, K. J. & Pakrasi, H. B. Genetic and immunological analyses of the cyanobacterium Synechocystis sp. PCC 6803 show that the protein encoded by the psbJ gene regulates the number of photosystem II centers in thylakoid membranes. J. Biol. Chem. 268, 1575–1579 (1993).
Nowaczyk, M. M. et al. Deletion of psbJ leads to accumulation of Psb27–Psb28 photosystem II complexes in Thermosynechococcus elongatus. BBA—Bioenergetics 1817, 1339–1345 (2012).
Ohad, I., Dal Bosco, C., Herrmann, R. G. & Meurer, J. Photosystem II proteins PsbL and PsbJ regulate electron flow to the plastoquinone pool. Biochemistry 43, 2297–2308 (2004).
Pakrasi, H. B., Williams, J. G. & Arntzen, C. J. Targeted mutagenesis of the psbE and psbF genes blocks photosynthetic electron transport: evidence for a functional role of cytochrome b559 in photosystem II. EMBO J. 7, 325 (1988).
Regel, R. E. et al. Deregulation of electron flow within photosystem II in the absence of the PsbJ protein. J. Biol. Chem. 276, 41473–41478 (2001).
Shinopoulos, K. E. & Brudvig, G. W. Cytochrome b559 and cyclic electron transfer within photosystem II. BBA—Bioenergetics 1817, 66–75 (2012).
Wassenaar, T. A., Ingólfsson, H. I., Böckmann, R. A., Tieleman, D. P. & Marrink, S. J. Computational lipidomics with insane: a versatile tool for generating custom membranes for molecular simulations. J. Chem. Theory Comput. 11, 2144–2155 (2015).
Sakurai, I. et al. Lipids in oxygen-evolving photosystem II complexes of cyanobacteria and higher plants. J. Biochem. 140, 201–209 (2006).
de Jong, D. H. et al. Improved parameters for the martini coarse-grained protein force field. J. Chem. Theory Comput. 9, 687–697 (2013).
Marrink, S. J., Risselada, H. J., Yefimov, S., Tieleman, D. P. & de Vries, A. H. The MARTINI force field: coarse grained model for biomolecular simulations. J. Phys. Chem. B 111, 7812–7824 (2007).
Periole, X., Cavalli, M., Marrink, S.-J. & Ceruso, M. A. Combining an elastic network with a coarse-grained molecular force field: structure, dynamics, and intermolecular recognition. J. Chem. Theory Comput. 5, 2531–2543 (2009).
López, C. A., Sovova, Z., van Eerden, F. J., de Vries, A. H. & Marrink, S. J. Martini force field parameters for glycolipids. J. Chem. Theory Comput. 9, 1694–1708 (2013).
Hess, B., Kutzner, C., van der Spoel, D. & Lindahl, E. GROMACS 4: algorithms for highly efficient, load-balanced, and scalable molecular simulation. J. Chem. Theory Comput. 4, 435–447 (2008).
de Jong, D. H., Baoukina, S. & Ingólfsson, H. I. Martini straight: boosting performance using a shorter cutoff and GPUs. Comp. Phys. Commn. 199, 1–7 (2016).
Bussi, G., Donadio, D. & Parrinello, M. Canonical sampling through velocity rescaling. J. Chem. Phys. 126, 014101 (2007).
Berendsen, H., Postma, J., van Gunsteren, W. F., DiNola, A. & Haak, J. R. Molecular dynamics with coupling to an external bath. J. Chem. Phys. 81, 3684–3690 (1984).
Ozer, G., Keyes, T., Quirk, S. & Hernandez, R. Multiple branched adaptive steered molecular dynamics. J. Chem. Phys. 141, 064101 (2014).
Humphrey, W., Dalke, A. & Schulten, K. VMD visual molecular dynamics. J. Molec. Graph. 14, 33–38 (1996).
Schrödinger, L. L. C. The PyMOL Molecular Graphics System, Version 188.8.131.52. (2010).
We thank Albert Guskov for helpful discussions and critical reading of the manuscript, and Marina Guskova for help with the illustrations. F.J.V.E. acknowledges funding from the Foundation of Fundamental Research of Matter (FOM), and S.J.M. acknowledges funding through an ERC Advanced Grant ‘COMP-MICR-CROW-MEM’.
The authors declare no competing financial interests.
Supplementary Figures, Supplementary Tables, Supplementary Note, Supplementary Methods and Supplementary References (PDF 3302 kb)
Opening of Channel III. During the 3 μs movie Cyt b 559β, Cyt b 559α and PsbJ move and tilt in the direction of subunit D2, while ycf12 and PsbK move in the opposite direction, resulting in the opening of channel III. Also visible is a PLQol occupying the QB site. The cofactor tail (red) sticks out of channel II, while its headgroup (orange) is located at the QB site. View is from within the membrane, with the subunits colored as in Figure 1b. (MOV 23750 kb)
Entering of PLQ inside the PLQ exchange cavity through Channel I. In this 35 μs movie a PLQ (blue, with headgroup in orange), enters the PLQ exchange cavity through channel I. Interestingly the PLQ adapts a folded conformation while passing through the channel. After passing through the channel, the cofactor diffuses around in the cavity. View is stromally on the protein, with the subunits colored as in Figure 1b. (MOV 21379 kb)
Leaving of PLQol through Channel III. The same PLQol (colored red, with its headgroup in orange) as in Figure 3b diffuses during 22 μs from the QB site, with its tail in Channel II, via Channel III into the thylakoid membrane. View is stromally with an angle, with the subunits colored as in Figure 1b. (MOV 18892 kb)
About this article
Site-directed mutagenesis of two amino acid residues in cytochrome b559 α subunit that interact with a phosphatidylglycerol molecule (PG772) induces quinone-dependent inhibition of photosystem II activity
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