Long Hai, Chang Christopher H, King Paul W, Ghirardi Maria L, Kim Kwiseon
National Renewable Energy Laboratory, Golden, Colorado, USA.
Biophys J. 2008 Oct;95(8):3753-66. doi: 10.1529/biophysj.107.127548. Epub 2008 Jul 11.
The [FeFe] hydrogenase from the green alga Chlamydomonas reinhardtii can catalyze the reduction of protons to hydrogen gas using electrons supplied from photosystem I and transferred via ferredoxin. To better understand the association of the hydrogenase and the ferredoxin, we have simulated the process over multiple timescales. A Brownian dynamics simulation method gave an initial thorough sampling of the rigid-body translational and rotational phase spaces, and the resulting trajectories were used to compute the occupancy and free-energy landscapes. Several important hydrogenase-ferredoxin encounter complexes were identified from this analysis, which were then individually simulated using atomistic molecular dynamics to provide more details of the hydrogenase and ferredoxin interaction. The ferredoxin appeared to form reasonable complexes with the hydrogenase in multiple orientations, some of which were good candidates for inclusion in a transition state ensemble of configurations for electron transfer.
来自绿藻莱茵衣藻的[FeFe]氢化酶能够利用光系统I提供并通过铁氧化还原蛋白传递的电子,催化质子还原为氢气。为了更好地理解氢化酶与铁氧化还原蛋白之间的关联,我们在多个时间尺度上对该过程进行了模拟。布朗动力学模拟方法对刚体平移和旋转相空间进行了初步的全面采样,所得轨迹用于计算占有率和自由能景观。通过该分析确定了几个重要的氢化酶-铁氧化还原蛋白相遇复合物,然后使用原子分子动力学对其进行单独模拟,以提供氢化酶与铁氧化还原蛋白相互作用的更多细节。铁氧化还原蛋白似乎能与氢化酶以多种取向形成合理的复合物,其中一些很可能包含在电子转移构型的过渡态系综中。