Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA; email:
Annu Rev Biophys. 2024 Jul;53(1):343-365. doi: 10.1146/annurev-biophys-071723-102519.
The structure and mechanism of the water-oxidation chemistry that occurs in photosystem II have been subjects of great interest. The advent of X-ray free electron lasers allowed the determination of structures of the stable intermediate states and of steps in the transitions between these intermediate states, bringing a new perspective to this field. The room-temperature structures collected as the photosynthetic water oxidation reaction proceeds in real time have provided important novel insights into the structural changes and the mechanism of the water oxidation reaction. The time-resolved measurements have also given us a view of how this reaction-which involves multielectron, multiproton processes-is facilitated by the interaction of the ligands and the protein residues in the oxygen-evolving complex. These structures have also provided a picture of the dynamics occurring in the channels within photosystem II that are involved in the transport of the substrate water to the catalytic center and protons to the bulk.
水氧化化学在光合作用 II 中发生的结构和机制一直是人们关注的焦点。X 射线自由电子激光的出现使得稳定中间态的结构以及这些中间态之间转变步骤的确定成为可能,为该领域带来了新的视角。在实时进行光合作用水氧化反应的过程中收集的室温结构,为水氧化反应的结构变化和机制提供了重要的新见解。时间分辨测量还使我们了解到,涉及多电子、多质子过程的这种反应是如何通过氧释放复合物中配体和蛋白质残基的相互作用来促进的。这些结构还提供了一个图片,展示了在参与将底物水输送到催化中心和质子输送到主体的通道中发生的动力学。