Task 3: Supramolecular organisation of membranes

1.         Adamska-Venkatesh, A., Simmons, T.R., Siebel, J.F., Artero, V., Fontecave, M., Reijerse, E. and Lubitz, W. (2015) Artificially maturated [FeFe] hydrogenase from Chlamydomonas reinhardtii: a HYSCORE and ENDOR study of a non-natural H-cluster. Phys Chem Chem Phys, 17, 5421-5430. http://www.ncbi.nlm.nih.gov/pubmed/25613229

2.         Aroua, S., Todorova, T.K., Hommes, P., Chamoreau, L.M., Reissig, H.U., Mougel, V. and Fontecave, M. (2017) Synthesis, Characterization, and DFT Analysis of Bis-Terpyridyl-Based Molecular Cobalt Complexes. Inorg Chem, 56, 5930-5940. http://www.ncbi.nlm.nih.gov/pubmed/28441011

3.         Aroua, S., Todorova, T.K., Mougel, V., Hommes, P., Reissig, H.-U. and Fontecave, M. (2017) New Cobalt-Bisterpyridyl Catalysts for Hydrogen Evolution Reaction. ChemCatChem, 9, 2099-2105. https://doi.org/10.1002/cctc.201700428

4.         Aussel, L., Pierrel, F., Loiseau, L., Lombard, M., Fontecave, M. and Barras, F. (2014) Biosynthesis and physiology of coenzyme Q in bacteria. Biochim Biophys Acta, 1837, 1004-1011. http://www.ncbi.nlm.nih.gov/pubmed/24480387

5.         Baaden, M. and Marrink, S.J. (2013) Coarse-grain modelling of protein-protein interactions. Curr Opin Struct Biol, 23, 878-886. http://www.ncbi.nlm.nih.gov/pubmed/24172141

6.         Bailleul, B., Berne, N., Murik, O., Petroutsos, D., Prihoda, J., Tanaka, A., Villanova, V., Bligny, R., Flori, S., Falconet, D. et al. (2015) Energetic coupling between plastids and mitochondria drives CO2 assimilation in diatoms. Nature, 524, 366-369. http://www.ncbi.nlm.nih.gov/pubmed/26168400

7.         Benbahouche, N.H., Iliopoulos, I., Torok, I., Marhold, J., Henri, J., Kajava, A.V., Farkas, R., Kempf, T., Schnolzer, M., Meyer, P. et al. (2014) Drosophila Spag is the homolog of RNA polymerase II-associated protein 3 (RPAP3) and recruits the heat shock proteins 70 and 90 (Hsp70 and Hsp90) during the assembly of cellular machineries. J Biol Chem, 289, 6236-6247. http://www.ncbi.nlm.nih.gov/pubmed/24394412

8.         Bergdoll, L., Ten Brink, F., Nitschke, W., Picot, D. and Baymann, F. (2016) From low- to high-potential bioenergetic chains: Thermodynamic constraints of Q-cycle function. Biochim Biophys Acta, 1857, 1569-1579. http://www.ncbi.nlm.nih.gov/pubmed/27328272

9.         Berger, H., De Mia, M., Morisse, S., Marchand, C.H., Lemaire, S.D., Wobbe, L. and Kruse, O. (2016) A Light Switch Based on Protein S-Nitrosylation Fine-Tunes Photosynthetic Light Harvesting in Chlamydomonas. Plant Physiol, 171, 821-832. http://www.ncbi.nlm.nih.gov/pubmed/27208221

10.       Boyer, B., Ezelin, J., Poulain, P., Saladin, A., Zacharias, M., Robert, C.H. and Prevost, C. (2015) An integrative approach to the study of filamentous oligomeric assemblies, with application to RecA. PLoS One, 10, e0116414. http://www.ncbi.nlm.nih.gov/pubmed/25785454

11.       Caserta, G., Adamska-Venkatesh, A., Pecqueur, L., Atta, M., Artero, V., Roy, S., Reijerse, E., Lubitz, W. and Fontecave, M. (2016) Chemical assembly of multiple metal cofactors: The heterologously expressed multidomain [FeFe]-hydrogenase from Megasphaera elsdenii. Biochim Biophys Acta, 1857, 1734-1740. http://www.ncbi.nlm.nih.gov/pubmed/27421233

12.       Caserta, G., Papini, C., Adamska-Venkatesh, A., Pecqueur, L., Sommer, C., Reijerse, E., Lubitz, W., Gauquelin, C., Meynial-Salles, I., Pramanik, D. et al. (2018) Engineering an [FeFe]-Hydrogenase: Do Accessory Clusters Influence O2 Resistance and Catalytic Bias? J Am Chem Soc, 140, 5516-5526. http://www.ncbi.nlm.nih.gov/pubmed/29595965

13.       Caserta, G., Pecqueur, L., Adamska-Venkatesh, A., Papini, C., Roy, S., Artero, V., Atta, M., Reijerse, E., Lubitz, W. and Fontecave, M. (2017) Structural and functional characterization of the hydrogenase-maturation HydF protein. Nat Chem Biol, 13, 779-784. http://www.ncbi.nlm.nih.gov/pubmed/28553946

14.       Caserta, G., Roy, S., Atta, M., Artero, V. and Fontecave, M. (2015) Artificial hydrogenases: biohybrid and supramolecular systems for catalytic hydrogen production or uptake. Curr Opin Chem Biol, 25, 36-47. http://www.ncbi.nlm.nih.gov/pubmed/25553541

15.       Chambers, M.B., Wang, X., Elgrishi, N., Hendon, C.H., Walsh, A., Bonnefoy, J., Canivet, J., Quadrelli, E.A., Farrusseng, D., Mellot-Draznieks, C. et al. (2015) Photocatalytic carbon dioxide reduction with rhodium-based catalysts in solution and heterogenized within metal-organic frameworks. ChemSusChem, 8, 603-608. http://www.ncbi.nlm.nih.gov/pubmed/25613479

16.       Chiricotto, M., Sterpone, F., Derreumaux, P. and Melchionna, S. (2016) Multiscale simulation of molecular processes in cellular environments. Philos Trans A Math Phys Eng Sci, 374. http://www.ncbi.nlm.nih.gov/pubmed/27698046

17.       Clowez, S., Godaux, D., Cardol, P., Wollman, F.A. and Rappaport, F. (2015) The involvement of hydrogen-producing and ATP-dependent NADPH-consuming pathways in setting the redox poise in the chloroplast of Chlamydomonas reinhardtii in anoxia. J Biol Chem, 290, 8666-8676. http://www.ncbi.nlm.nih.gov/pubmed/25691575

18.       Colloc'h, N., Sacquin-Mora, S., Avella, G., Dhaussy, A.C., Prange, T., Vallone, B. and Girard, E. (2017) Determinants of neuroglobin plasticity highlighted by joint coarse-grained simulations and high pressure crystallography. Sci Rep, 7, 1858. http://www.ncbi.nlm.nih.gov/pubmed/28500341

19.       Dautant, A., Meyer, P. and Georgescauld, F. (2017) Hydrogen/Deuterium Exchange Mass Spectrometry Reveals Mechanistic Details of Activation of Nucleoside Diphosphate Kinases by Oligomerization. Biochemistry, 56, 2886-2896. http://www.ncbi.nlm.nih.gov/pubmed/28481113

20.       Dumas, L., Zito, F., Auroy, P., Johnson, X., Peltier, G. and Alric, J. (2018) Structure-Function Analysis of Chloroplast Proteins via Random Mutagenesis Using Error-Prone PCR. Plant Physiol, 177, 465-475. http://www.ncbi.nlm.nih.gov/pubmed/29703866

21.       Dumas, L., Zito, F., Blangy, S., Auroy, P., Johnson, X., Peltier, G. and Alric, J. (2017) A stromal region of cytochrome b6f subunit IV is involved in the activation of the Stt7 kinase in Chlamydomonas. Proc Natl Acad Sci U S A, 114, 12063-12068. http://www.ncbi.nlm.nih.gov/pubmed/29078388

22.       Elgrishi, N., Artero, V. and Fontecave, M. (2013) Activation du dioxyde de carbone: enzymes, catalyseurs bioinspirés et photosynthèse artificielle. L’Actualité Chimique 371-372, 95-100.

23.       Elgrishi, N., Chambers, M.B., Artero, V. and Fontecave, M. (2014) Terpyridine complexes of first row transition metals and electrochemical reduction of CO(2) to CO. Phys Chem Chem Phys, 16, 13635-13644. http://www.ncbi.nlm.nih.gov/pubmed/24651983

24.       Elgrishi, N., Chambers, M.B. and Fontecave, M. (2015) Turning it off! Disfavouring hydrogen evolution to enhance selectivity for CO production during homogeneous CO2 reduction by cobalt-terpyridine complexes. Chem Sci, 6, 2522-2531. http://www.ncbi.nlm.nih.gov/pubmed/28706660

25.       Elgrishi, N., Chambers, M.B., Wang, X. and Fontecave, M. (2017) Molecular polypyridine-based metal complexes as catalysts for the reduction of CO2. Chem Soc Rev, 46, 761-796. http://www.ncbi.nlm.nih.gov/pubmed/28084485

26.       Elgrishi, N., Griveau, S., Chambers, M.B., Bedioui, F. and Fontecave, M. (2015) Versatile functionalization of carbon electrodes with a polypyridine ligand: metallation and electrocatalytic H(+) and CO2 reduction. Chem Commun (Camb), 51, 2995-2998. http://www.ncbi.nlm.nih.gov/pubmed/25597872

27.       Fogeron, T., Porcher, J.P., Gomez-Mingot, M., Todorova, T.K., Chamoreau, L.M., Mellot-Draznieks, C., Li, Y. and Fontecave, M. (2016) A cobalt complex with a bioinspired molybdopterin-like ligand: a catalyst for hydrogen evolution. Dalton Trans, 45, 14754-14763. http://www.ncbi.nlm.nih.gov/pubmed/27426738

28.       Fogeron, T., Retailleau, P., Chamoreau, L.M., Fontecave, M. and Li, Y. (2017) The unusual ring scission of a quinoxaline-pyran-fused dithiolene system related to molybdopterin. Dalton Trans, 46, 4161-4164. http://www.ncbi.nlm.nih.gov/pubmed/28277588

29.       Fogeron, T., Todorova, T.K., Porcher, J.-P., Gomez-Mingot, M., Chamoreau, L.-M., Mellot-Draznieks, C., Li, Y. and Fontecave, M. (2018) A Bioinspired Nickel(bis-dithiolene) Complex as a Homogeneous Catalyst for Carbon Dioxide Electroreduction. ACS Catalysis, 8, 2030-2038. https://doi.org/10.1021/acscatal.7b03383

30.       Fortunato, A.E., Jaubert, M., Enomoto, G., Bouly, J.P., Raniello, R., Thaler, M., Malviya, S., Bernardes, J.S., Rappaport, F., Gentili, B. et al. (2016) Diatom Phytochromes Reveal the Existence of Far-Red-Light-Based Sensing in the Ocean. Plant Cell, 28, 616-628. http://www.ncbi.nlm.nih.gov/pubmed/26941092

31.       Fu, H., Cai, W., Henin, J., Roux, B. and Chipot, C. (2017) New Coarse Variables for the Accurate Determination of Standard Binding Free Energies. J Chem Theory Comput, 13, 5173-5178. http://www.ncbi.nlm.nih.gov/pubmed/28965398

32.       Fu, H.Y., Picot, D., Choquet, Y., Longatte, G., Sayegh, A., Delacotte, J., Guille-Collignon, M., Lemaitre, F., Rappaport, F. and Wollman, F.A. (2017) Redesigning the QA binding site of Photosystem II allows reduction of exogenous quinones. Nat Commun, 8, 15274. http://www.ncbi.nlm.nih.gov/pubmed/28466860

33.       Goudy, V., Maynadié, J., Goff, X.L., Meyer, D. and Fontecave, M. (2016) Synthesis, electrochemical and spectroscopic properties of ruthenium(ii) complexes containing 2,6-di(1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl)aryl ligands. New Journal of Chemistry, 40, 1704-1714. http://dx.doi.org/10.1039/C5NJ02280K

34.       Hitaishi, V., Clement, R., Bourassin, N., Baaden, M., de Poulpiquet, A., Sacquin-Mora, S., Ciaccafava, A. and Lojou, E. (2018) Controlling Redox Enzyme Orientation at Planar Electrodes. Catalysts, 8, 192. http://www.mdpi.com/2073-4344/8/5/192

35.       Huan, T.N., Andreiadis, E.S., Heidkamp, J., Simon, P., Derat, E., Cobo, S., Royal, G., Bergmann, A., Strasser, P., Dau, H. et al. (2015) From molecular copper complexes to composite electrocatalytic materials for selective reduction of CO2 to formic acid. Journal of Materials Chemistry A, 3, 3901-3907. http://dx.doi.org/10.1039/C4TA07022D

36.       Huan, T.N., Prakash, P., Simon, P., Rousse, G., Xu, X., Artero, V., Gravel, E., Doris, E. and Fontecave, M. (2016) CO2 Reduction to CO in Water: Carbon Nanotube-Gold Nanohybrid as a Selective and Efficient Electrocatalyst. ChemSusChem, 9, 2317-2320. http://www.ncbi.nlm.nih.gov/pubmed/27492905

37.       Huan, T.N., Simon, P., Benayad, A., Guetaz, L., Artero, V. and Fontecave, M. (2016) Cu/Cu2 O Electrodes and CO2 Reduction to Formic Acid: Effects of Organic Additives on Surface Morphology and Activity. Chemistry, 22, 14029-14035. http://www.ncbi.nlm.nih.gov/pubmed/27516360

38.       Huan, T.N., Simon, P., Rousse, G., Genois, I., Artero, V. and Fontecave, M. (2017) Porous dendritic copper: an electrocatalyst for highly selective CO2 reduction to formate in water/ionic liquid electrolyte. Chem Sci, 8, 742-747. http://www.ncbi.nlm.nih.gov/pubmed/28451222

39.       Ismail, A., Leroux, V., Smadja, M., Gonzalez, L., Lombard, M., Pierrel, F., Mellot-Draznieks, C. and Fontecave, M. (2016) Coenzyme Q Biosynthesis: Evidence for a Substrate Access Channel in the FAD-Dependent Monooxygenase Coq6. PLOS Computational Biology, 12, e1004690. https://doi.org/10.1371/journal.pcbi.1004690

40.       Johnson, X., Steinbeck, J., Dent, R.M., Takahashi, H., Richaud, P., Ozawa, S., Houille-Vernes, L., Petroutsos, D., Rappaport, F., Grossman, A.R. et al. (2014) Proton gradient regulation 5-mediated cyclic electron flow under ATP- or redox-limited conditions: a study of DeltaATpase pgr5 and DeltarbcL pgr5 mutants in the green alga Chlamydomonas reinhardtii. Plant Physiol, 165, 438-452. http://www.ncbi.nlm.nih.gov/pubmed/24623849

41.       Loiseau, L., Fyfe, C., Aussel, L., Hajj Chehade, M., Hernandez, S.B., Faivre, B., Hamdane, D., Mellot-Draznieks, C., Rascalou, B., Pelosi, L. et al. (2017) The UbiK protein is an accessory factor necessary for bacterial ubiquinone (UQ) biosynthesis and forms a complex with the UQ biogenesis factor UbiJ. J Biol Chem, 292, 11937-11950. http://www.ncbi.nlm.nih.gov/pubmed/28559279

42.       Longatte, G., Fu, H.Y., Buriez, O., Labbe, E., Wollman, F.A., Amatore, C., Rappaport, F., Guille-Collignon, M. and Lemaitre, F. (2015) Evaluation of photosynthetic electrons derivation by exogenous redox mediators. Biophys Chem, 205, 1-8. http://www.ncbi.nlm.nih.gov/pubmed/26051794

43.       Longatte, G., Guille-Collignon, M. and Lemaitre, F. (2017) Electrocatalytic Mechanism Involving Michaelis-Menten Kinetics at the Preparative Scale: Theory and Applicability to Photocurrents from a Photosynthetic Algae Suspension With Quinones. Chemphyschem, 18, 2643-2650. http://www.ncbi.nlm.nih.gov/pubmed/28618080

44.       Longatte, G., Rappaport, F., Wollman, F.-A., Guille-Collignon, M. and Lemaître, F. (2017) Electrochemical Harvesting of Photosynthetic Electrons from Unicellular Algae Population at the Preparative Scale by Using 2,6-dichlorobenzoquinone. Electrochimica Acta, 236, 337-342. http://www.sciencedirect.com/science/article/pii/S0013468617306047

45.       Longatte, G., Rappaport, F., Wollman, F.A., Guille-Collignon, M. and Lemaitre, F. (2016) Mechanism and analyses for extracting photosynthetic electrons using exogenous quinones - what makes a good extraction pathway? Photochem Photobiol Sci, 15, 969-979. http://www.ncbi.nlm.nih.gov/pubmed/27411477

46.       Longatte, G., Sayegh, A., Delacotte, J., Rappaport, F., Wollman, F.-A., Guille Collignon, M. and Lemaître, F. (2018) Investigation of Photocurrents Resulting from Living Unicellular Algae Suspension with Quinones over Time. Chemical Science. http://dx.doi.org/10.1039/C8SC03058H

47.       Malnoe, A., Wang, F., Girard-Bascou, J., Wollman, F.A. and de Vitry, C. (2014) Thylakoid FtsH protease contributes to photosystem II and cytochrome b6f remodeling in Chlamydomonas reinhardtii under stress conditions. Plant Cell, 26, 373-390. http://www.ncbi.nlm.nih.gov/pubmed/24449688

48.       Man, V.H., Nguyen, P.H. and Derreumaux, P. (2017) Conformational Ensembles of the Wild-Type and S8C Abeta1-42 Dimers. J Phys Chem B, 121, 2434-2442. http://www.ncbi.nlm.nih.gov/pubmed/28245647

49.       Michelet, L., Zaffagnini, M., Morisse, S., Sparla, F., Perez-Perez, M.E., Francia, F., Danon, A., Marchand, C.H., Fermani, S., Trost, P. et al. (2013) Redox regulation of the Calvin-Benson cycle: something old, something new. Front Plant Sci, 4, 470. http://www.ncbi.nlm.nih.gov/pubmed/24324475

50.       Molza, A.E., Ferey, N., Czjzek, M., Le Rumeur, E., Hubert, J.F., Tek, A., Laurent, B., Baaden, M. and Delalande, O. (2014) Innovative interactive flexible docking method for multi-scale reconstruction elucidates dystrophin molecular assembly. Faraday Discuss, 169, 45-62. http://www.ncbi.nlm.nih.gov/pubmed/25340652

51.       Nawrocki, W.J., Santabarbara, S., Mosebach, L., Wollman, F.A. and Rappaport, F. (2016) State transitions redistribute rather than dissipate energy between the two photosystems in Chlamydomonas. Nat Plants, 2, 16031. http://www.ncbi.nlm.nih.gov/pubmed/27249564

52.       Nawrocki, W.J., Tourasse, N.J., Taly, A., Rappaport, F. and Wollman, F.A. (2015) The plastid terminal oxidase: its elusive function points to multiple contributions to plastid physiology. Annu Rev Plant Biol, 66, 49-74. http://www.ncbi.nlm.nih.gov/pubmed/25580838

53.       Nilsson, H., Cournac, L., Rappaport, F., Messinger, J. and Lavergne, J. (2016) Estimation of the driving force for dioxygen formation in photosynthesis. Biochim Biophys Acta, 1857, 23-33. http://www.ncbi.nlm.nih.gov/pubmed/26435390

54.       Nilsson, H., Rappaport, F., Boussac, A. and Messinger, J. (2014) Substrate-water exchange in photosystem II is arrested before dioxygen formation. Nat Commun, 5, 4305. http://www.ncbi.nlm.nih.gov/pubmed/24993602

55.       Oteri, F., Baaden, M., Lojou, E. and Sacquin-Mora, S. (2014) Multiscale simulations give insight into the hydrogen in and out pathways of [NiFe]-hydrogenases from Aquifex aeolicus and Desulfovibrio fructosovorans. J Phys Chem B, 118, 13800-13811. http://www.ncbi.nlm.nih.gov/pubmed/25399809

56.       Oteri, F., Ciaccafava, A., de Poulpiquet, A., Baaden, M., Lojou, E. and Sacquin-Mora, S. (2014) The weak, fluctuating, dipole moment of membrane-bound hydrogenase from Aquifex aeolicus accounts for its adaptability to charged electrodes. Phys Chem Chem Phys, 16, 11318-11322. http://www.ncbi.nlm.nih.gov/pubmed/24789038

57.       Porcher, J.P., Fogeron, T., Gomez-Mingot, M., Chamoreau, L.M., Li, Y. and Fontecave, M. (2016) Synthesis and Reactivity of a Bio-inspired Dithiolene Ligand and its Mo Oxo Complex. Chemistry, 22, 4447-4453. http://www.ncbi.nlm.nih.gov/pubmed/26880579

58.       Porcher, J.P., Fogeron, T., Gomez-Mingot, M., Derat, E., Chamoreau, L.M., Li, Y. and Fontecave, M. (2015) A Bioinspired Molybdenum Complex as a Catalyst for the Photo- and Electroreduction of Protons. Angew Chem Int Ed Engl, 54, 14090-14093. http://www.ncbi.nlm.nih.gov/pubmed/26404460

59.       Roy, S., Sharma, B., Pecaut, J., Simon, P., Fontecave, M., Tran, P.D., Derat, E. and Artero, V. (2017) Molecular Cobalt Complexes with Pendant Amines for Selective Electrocatalytic Reduction of Carbon Dioxide to Formic Acid. J Am Chem Soc, 139, 3685-3696. http://www.ncbi.nlm.nih.gov/pubmed/28206761

60.       Santabarbara, S., Bullock, B., Rappaport, F. and Redding, K.E. (2015) Controlling electron transfer between the two cofactor chains of photosystem I by the redox state of one of their components. Biophys J, 108, 1537-1547. http://www.ncbi.nlm.nih.gov/pubmed/25809266

61.       Sommer, C., Rumpel, S., Roy, S., Fares, C., Artero, V., Fontecave, M., Reijerse, E. and Lubitz, W. (2018) Spectroscopic investigations of a semi-synthetic [FeFe] hydrogenase with propane di-selenol as bridging ligand in the binuclear subsite: comparison to the wild type and propane di-thiol variants. J Biol Inorg Chem. http://www.ncbi.nlm.nih.gov/pubmed/29627860

62.       Sterpone, F., Nguyen, P.H., Kalimeri, M. and Derreumaux, P. (2013) Importance of the ion-pair interactions in the OPEP coarse-grained force field: parametrization and validation. J Chem Theory Comput, 9, 4574-4584. http://www.ncbi.nlm.nih.gov/pubmed/25419192

63.       Sugiura, M., Azami, C., Koyama, K., Rutherford, A.W., Rappaport, F. and Boussac, A. (2014) Modification of the pheophytin redox potential in Thermosynechococcus elongatus Photosystem II with PsbA3 as D1. Biochim Biophys Acta, 1837, 139-148. http://www.ncbi.nlm.nih.gov/pubmed/24060528

64.       Sugiura, M., Ozaki, Y., Nakamura, M., Cox, N., Rappaport, F. and Boussac, A. (2014) The D1-173 amino acid is a structural determinant of the critical interaction between D1-Tyr161 (TyrZ) and D1-His190 in Photosystem II. Biochim Biophys Acta, 1837, 1922-1931. http://www.ncbi.nlm.nih.gov/pubmed/25193561

65.       Takahashi, H., Clowez, S., Wollman, F.A., Vallon, O. and Rappaport, F. (2013) Cyclic electron flow is redox-controlled but independent of state transition. Nat Commun, 4, 1954. http://www.ncbi.nlm.nih.gov/pubmed/23760547

66.       Takahashi, H., Schmollinger, S., Lee, J.H., Schroda, M., Rappaport, F., Wollman, F.A. and Vallon, O. (2016) PETO Interacts with Other Effectors of Cyclic Electron Flow in Chlamydomonas. Mol Plant, 9, 558-568. http://www.ncbi.nlm.nih.gov/pubmed/26768121

67.       Vermeglio, A., Lavergne, J. and Rappaport, F. (2016) Connectivity of the intracytoplasmic membrane of Rhodobacter sphaeroides: a functional approach. Photosynth Res, 127, 13-24. http://www.ncbi.nlm.nih.gov/pubmed/25512104

68.       Wang, M., Baaden, M., Wang, J. and Liang, Z. (2014) A cooperative mechanism of clotrimazoles in P450 revealed by the dissociation picture of clotrimazole from P450. J Chem Inf Model, 54, 1218-1225. http://www.ncbi.nlm.nih.gov/pubmed/24611729

69.       Wang, X., Wisser, F.M., Canivet, J., Fontecave, M. and Mellot-Draznieks, C. (2018) Immobilization of a Full Photosystem in the Large-Pore MIL-101 Metal-Organic Framework for CO2 reduction. ChemSusChem. https://www.ncbi.nlm.nih.gov/pubmed/29978953

70.       Wei, L., Derrien, B., Gautier, A., Houille-Vernes, L., Boulouis, A., Saint-Marcoux, D., Malnoe, A., Rappaport, F., de Vitry, C., Vallon, O. et al. (2014) Nitric oxide-triggered remodeling of chloroplast bioenergetics and thylakoid proteins upon nitrogen starvation in Chlamydomonas reinhardtii. Plant Cell, 26, 353-372. http://www.ncbi.nlm.nih.gov/pubmed/24474630

71.       Yadav, D., Lacombat, F., Dozova, N., Rappaport, F., Plaza, P. and Espagne, A. (2015) Real-time monitoring of chromophore isomerization and deprotonation during the photoactivation of the fluorescent protein Dronpa. J Phys Chem B, 119, 2404-2414. http://www.ncbi.nlm.nih.gov/pubmed/25325882

72.       Yoo, B.K., Lamarre, I., Martin, J.L., Rappaport, F. and Negrerie, M. (2015) Motion of proximal histidine and structural allosteric transition in soluble guanylate cyclase. Proc Natl Acad Sci U S A, 112, E1697-1704. http://www.ncbi.nlm.nih.gov/pubmed/25831539

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