Askerka Mikhail, Vinyard David J, Wang Jimin, Brudvig Gary W, Batista Victor S
Department of Chemistry, Yale University , New Haven, Connecticut 06520-8107, United States .
Biochemistry. 2015 Mar 10;54(9):1713-6. doi: 10.1021/acs.biochem.5b00089. Epub 2015 Feb 27.
A recent femtosecond X-ray diffraction study produced the first high-resolution structural model of the oxygen-evolving complex of photosystem II that is free of radiation-induced manganese reduction (Protein Data Bank entries 4UB6 and 4UB8 ). We find, however, that the model does not match extended X-ray absorption fine structure and QM/MM data for the S1 state. This is attributed to uncertainty about the positions of oxygen atoms that remain partially unresolved, even at 1.95 Å resolution, next to the heavy manganese centers. In addition, the photosystem II crystals may contain significant amounts of the S0 state, because of extensive dark adaptation prior to data collection.
最近的一项飞秒X射线衍射研究得出了光系统II析氧复合物的首个高分辨率结构模型,该模型不存在辐射诱导的锰还原现象(蛋白质数据库条目4UB6和4UB8)。然而,我们发现该模型与S1态的扩展X射线吸收精细结构和量子力学/分子力学数据不匹配。这归因于即使在1.95埃分辨率下,紧邻重锰中心的部分未完全解析的氧原子位置存在不确定性。此外,由于在数据收集之前进行了长时间的暗适应,光系统II晶体可能含有大量的S0态。