Structural and quantum chemical basis for OCP-mediated quenching of phycobilisomes
Structural and quantum chemical basis for OCP-mediated quenching of phycobilisomes
Cyanobacteria employ large antenna complexes called phycobilisomes (PBS) for light harvesting. However, intense light triggers non-photochemical quenching, where the Orange Carotenoid Protein (OCP) binds to PBS, dissipating excess energy as heat. The mechanism of efficiently transferring energy from phycocyanobilins in PBS to canthaxanthin in OCP remains insufficiently understood. Using advanced cryogenic-electron microscopy, we unveiled the OCP-PBS complex structure at 1.6-2.1 ? resolution, showcasing its inherent flexibility. Employing multiscale quantum chemistry, we disclosed the quenching mechanism. Identifying key protein residues, we clarified how canthaxanthin's transition dipole moment in its lowest-energy dark state becomes large enough for efficient energy transfer from phycocyanobilins. Our energy transfer model offers a detailed understanding of the atomic determinants of light harvesting regulation and antenna architecture in cyanobacteria.
Sauer Paul V、Cupellini Lorenzo、Bondanza Mattia、Dominguez Martin Maria Agustina、Bina David、Koh Adrian Fujiet、Nogales Eva、Polivka Tomas、Kerfeld Cheryl A、Kotecha Abhay、Mennucci Benedetta、Greber Basil J、Sutter Markus、Kirst Henning
生物物理学
Sauer Paul V,Cupellini Lorenzo,Bondanza Mattia,Dominguez Martin Maria Agustina,Bina David,Koh Adrian Fujiet,Nogales Eva,Polivka Tomas,Kerfeld Cheryl A,Kotecha Abhay,Mennucci Benedetta,Greber Basil J,Sutter Markus,Kirst Henning.Structural and quantum chemical basis for OCP-mediated quenching of phycobilisomes[EB/OL].(2025-03-28)[2025-06-06].https://www.biorxiv.org/content/10.1101/2023.09.30.560311.点此复制
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