Division of Environmental Photobiology, National Institute for Basic Biology, Okazaki, Japan.
Department of Basic Biology, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Japan.
FEBS Lett. 2019 May;593(10):1072-1079. doi: 10.1002/1873-3468.13394. Epub 2019 May 11.
Photosystem II (PSII) splits water and drives electron transfer to plastoquinone via photochemical reactions using light energy. It is surrounded by light-harvesting complex II (LHCII) to form the PSII-LHCII supercomplex. Complete characterization of its structure and function has, however, been hampered due to instability of the complex in the presence of detergent. To overcome this problem, we developed a new procedure for purifying the PSII-LHCII supercomplexes of Chlamydomonas reinhardtii employing amphipol A8-35. The obtained supercomplexes showed little LHCII dissociation even 4 days after purification. Oxygen-evolving activity was retained within amphipol if the extrinsic polypeptides were kept associated by betaine. Electron microscopy revealed that this method also improved structural uniformity and that the major organization was C S M L .
光系统 II(PSII)通过利用光能进行光化学反应分裂水并驱动电子向质体醌转移。它被捕光复合物 II(LHCII)包围,形成 PSII-LHCII 超复合物。然而,由于在去污剂存在下该复合物的不稳定性,其结构和功能的完全表征受到了阻碍。为了克服这个问题,我们开发了一种使用 Amphipol A8-35 纯化衣藻 PSII-LHCII 超复合物的新程序。即使在纯化后 4 天,获得的超复合物显示出很少的 LHCII 解离。如果通过甜菜碱使外在多肽保持关联,则氧释放活性保留在 Amphipol 中。电子显微镜显示,这种方法还提高了结构的均匀性,主要组织为 C S M L。