School of Science, Constructor University, Campus Ring 1, 28759 Bremen, Germany.
J Phys Chem B. 2024 May 30;128(21):5201-5217. doi: 10.1021/acs.jpcb.4c01637. Epub 2024 May 16.
In this study, the site energy fluctuations, energy transfer dynamics, and some spectroscopic properties of the minor light-harvesting complex CP24 in a membrane environment were determined. For this purpose, a 3 μs-long classical molecular dynamics simulation was performed for the CP24 complex. Furthermore, using the density functional tight binding/molecular mechanics molecular dynamics (DFTB/MM MD) approach, we performed excited state calculations for the chlorophyll a and chlorophyll b molecules in the complex starting from five different positions of the MD trajectory. During the extended simulations, we observed variations in the site energies of the different sets as a result of the fluctuating protein environment. In particular, a water coordination to Chl-b 608 occurred only after about 1 μs in the simulations, demonstrating dynamic changes in the environment of this pigment. From the classical and the DFTB/MM MD simulations, spectral densities and the (time-dependent) Hamiltonian of the complex were determined. Based on these results, three independent strongly coupled chlorophyll clusters were revealed within the complex. In addition, absorption and fluorescence spectra were determined together with the exciton relaxation dynamics, which reasonably well agrees with experimental time scales.
在这项研究中,确定了膜环境中次要光捕获复合物 CP24 的位能波动、能量转移动力学和一些光谱性质。为此,对 CP24 复合物进行了长达 3 μs 的经典分子动力学模拟。此外,我们使用密度泛函紧束缚/分子力学分子动力学(DFTB/MM MD)方法,从 MD 轨迹的五个不同位置开始,对复合物中的叶绿素 a 和叶绿素 b 分子进行激发态计算。在扩展模拟过程中,我们观察到不同集合的位能由于不断变化的蛋白质环境而发生变化。特别是,在模拟中大约 1 μs 后,Chl-b608 才与水分子配位,这表明该色素的环境发生了动态变化。从经典和 DFTB/MM MD 模拟中,确定了复合物的光谱密度和(时变)哈密顿量。基于这些结果,揭示了复合物内三个独立的强耦合叶绿素簇。此外,还确定了吸收和荧光光谱以及激子弛豫动力学,这些结果与实验时间尺度相当吻合。