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费纳-马修斯-奥尔森复合物中振动能量转移与局域化的非线性网络模型分析

Nonlinear network model analysis of vibrational energy transfer and localisation in the Fenna-Matthews-Olson complex.

作者信息

Morgan Sarah E, Cole Daniel J, Chin Alex W

机构信息

Theory of Condensed Matter Group, Physics Department, University of Cambridge, CB3 0HE, United Kingdom.

School of Chemistry, Newcastle University, Newcastle upon Tyne, NE1 7RU, United Kingdom.

出版信息

Sci Rep. 2016 Nov 9;6:36703. doi: 10.1038/srep36703.

DOI:10.1038/srep36703
PMID:27827409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5101523/
Abstract

Collective protein modes are expected to be important for facilitating energy transfer in the Fenna-Matthews-Olson (FMO) complex of photosynthetic green sulphur bacteria, however to date little work has focussed on the microscopic details of these vibrations. The nonlinear network model (NNM) provides a computationally inexpensive approach to studying vibrational modes at the microscopic level in large protein structures, whilst incorporating anharmonicity in the inter-residue interactions which can influence protein dynamics. We apply the NNM to the entire trimeric FMO complex and find evidence for the existence of nonlinear discrete breather modes. These modes tend to transfer energy to the highly connected core pigments, potentially opening up alternative excitation energy transfer routes through their influence on pigment properties. Incorporating localised modes based on these discrete breathers in the optical spectra calculations for FMO using ab initio site energies and excitonic couplings can substantially improve their agreement with experimental results.

摘要

集体蛋白质模式有望对促进光合绿硫细菌的芬纳 - 马修斯 - 奥尔森(FMO)复合物中的能量转移起到重要作用,然而迄今为止,很少有工作聚焦于这些振动的微观细节。非线性网络模型(NNM)提供了一种计算成本低廉的方法,用于在大型蛋白质结构的微观层面研究振动模式,同时在残基间相互作用中纳入非谐性,这会影响蛋白质动力学。我们将NNM应用于整个三聚体FMO复合物,并找到了非线性离散呼吸子模式存在的证据。这些模式倾向于将能量转移到高度连接的核心色素上,可能通过它们对色素性质的影响开辟替代的激发能量转移途径。在使用从头算位点能量和激子耦合进行FMO光谱计算时,基于这些离散呼吸子纳入局部模式,可以显著提高它们与实验结果的一致性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/ff1287bb550d/srep36703-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/bff1a9209ba3/srep36703-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/367ea51f2523/srep36703-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/8f9b6f217a49/srep36703-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/ff1287bb550d/srep36703-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/bff1a9209ba3/srep36703-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/367ea51f2523/srep36703-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/8f9b6f217a49/srep36703-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299c/5101523/ff1287bb550d/srep36703-f4.jpg

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本文引用的文献

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Protein Effects on the Optical Spectrum of the Fenna-Matthews-Olson Complex from Fully Quantum Chemical Calculations.基于全量子化学计算的蛋白质对芬纳-马修斯-奥尔森复合物光谱的影响
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