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本文引用的文献

1
Strain specific differences in rates of Photosystem II repair in picocyanobacteria correlate to differences in FtsH protein levels and isoform expression patterns.在蓝细菌中,光系统 II 修复的速率存在种间差异,这与 FtsH 蛋白水平和同工型表达模式的差异有关。
PLoS One. 2018 Dec 19;13(12):e0209115. doi: 10.1371/journal.pone.0209115. eCollection 2018.
2
The PRIDE database and related tools and resources in 2019: improving support for quantification data.PRIDE 数据库及相关工具和资源在 2019 年的进展:提高定量数据支持。
Nucleic Acids Res. 2019 Jan 8;47(D1):D442-D450. doi: 10.1093/nar/gky1106.
3
Reactive oxygen species leave a damage trail that reveals water channels in Photosystem II.活性氧会留下一条损伤轨迹,揭示光系统 II 中的水通道。
Sci Adv. 2017 Nov 17;3(11):eaao3013. doi: 10.1126/sciadv.aao3013. eCollection 2017 Nov.
4
Glutamate promotes SSB protein-protein Interactions via intrinsically disordered regions.谷氨酸通过内在无序区域促进单链结合蛋白(SSB)的蛋白质-蛋白质相互作用。
J Mol Biol. 2017 Sep 1;429(18):2790-2801. doi: 10.1016/j.jmb.2017.07.021. Epub 2017 Aug 3.
5
Structural insights into the light-driven auto-assembly process of the water-oxidizing MnCaO-cluster in photosystem II.结构洞察光驱动的水氧化 MnCaO 簇在光系统 II 中的自动组装过程。
Elife. 2017 Jul 18;6:e26933. doi: 10.7554/eLife.26933.
6
Amino acid oxidation of the D1 and D2 proteins by oxygen radicals during photoinhibition of Photosystem II.在光系统II光抑制过程中,氧自由基对D1和D2蛋白的氨基酸氧化作用。
Proc Natl Acad Sci U S A. 2017 Mar 14;114(11):2988-2993. doi: 10.1073/pnas.1618922114. Epub 2017 Mar 6.
7
Light-induced structural changes and the site of O=O bond formation in PSII caught by XFEL.X 射线自由电子激光捕获 PSII 中光诱导结构变化和 O=O 键形成的位置。
Nature. 2017 Mar 2;543(7643):131-135. doi: 10.1038/nature21400. Epub 2017 Feb 20.
8
Mass spectrometry-based cross-linking study shows that the Psb28 protein binds to cytochrome in Photosystem II.基于质谱的交联研究表明,Psb28蛋白与光系统II中的细胞色素结合。
Proc Natl Acad Sci U S A. 2017 Feb 28;114(9):2224-2229. doi: 10.1073/pnas.1620360114. Epub 2017 Feb 13.
9
Production of Reactive Oxygen Species by Photosystem II as a Response to Light and Temperature Stress.光系统II产生活性氧作为对光和温度胁迫的响应。
Front Plant Sci. 2016 Dec 26;7:1950. doi: 10.3389/fpls.2016.01950. eCollection 2016.
10
Structure of photosystem II and substrate binding at room temperature.室温下光系统II的结构与底物结合
Nature. 2016 Dec 15;540(7633):453-457. doi: 10.1038/nature20161. Epub 2016 Nov 21.

一种新型的叶绿素蛋白复合物在光系统 II 的修复循环中。

A novel chlorophyll protein complex in the repair cycle of photosystem II.

机构信息

Department of Biology, Washington University in St. Louis, St. Louis, MO 63130.

Center for Solar Energy & Energy Storage, Department of Energy, Environmental, & Chemical Engineering, Washington University in St. Louis, St. Louis, MO 63130.

出版信息

Proc Natl Acad Sci U S A. 2019 Oct 22;116(43):21907-21913. doi: 10.1073/pnas.1909644116. Epub 2019 Oct 8.

DOI:10.1073/pnas.1909644116
PMID:31594847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6815111/
Abstract

In oxygenic photosynthetic organisms, photosystem II (PSII) is a unique membrane protein complex that catalyzes light-driven oxidation of water. PSII undergoes frequent damage due to its demanding photochemistry. It must undergo a repair and reassembly process following photodamage, many facets of which remain unknown. We have discovered a PSII subcomplex that lacks 5 key PSII core reaction center polypeptides: D1, D2, PsbE, PsbF, and PsbI. This pigment-protein complex does contain the PSII core antenna proteins CP47 and CP43, as well as most of their associated low molecular mass subunits, and the assembly factor Psb27. Immunoblotting, mass spectrometry, and ultrafast spectroscopic results support the absence of a functional reaction center in this complex, which we call the "no reaction center" complex (NRC). Analytical ultracentrifugation and clear native PAGE analysis show that NRC is a stable pigment-protein complex and not a mixture of free CP47 and CP43 proteins. NRC appears in higher abundance in cells exposed to high light and impaired protein synthesis, and genetic deletion of PsbO on the PSII luminal side results in an increased NRC population, indicative that NRC forms in response to photodamage as part of the PSII repair process. Our finding challenges the current model of the PSII repair cycle and implies an alternative PSII repair strategy. Formation of this complex may maximize PSII repair economy by preserving intact PSII core antennas in a single complex available for PSII reassembly, minimizing the risk of randomly diluting multiple recycling components in the thylakoid membrane following a photodamage event.

摘要

在产氧光合作用生物中,光系统 II(PSII)是一种独特的膜蛋白复合物,它催化光驱动水的氧化。由于其苛刻的光化学特性,PSII 经常受到损伤。在光损伤后,它必须经历一个修复和重新组装的过程,其中许多方面仍然未知。我们发现了一种 PSII 亚复合物,它缺乏 5 种关键的 PSII 核心反应中心多肽:D1、D2、PsbE、PsbF 和 PsbI。这个色素-蛋白复合物确实包含 PSII 核心天线蛋白 CP47 和 CP43,以及它们的大多数相关的低分子量亚基,以及组装因子 Psb27。免疫印迹、质谱和超快光谱结果支持这个复合物中不存在功能反应中心,我们称之为“无反应中心”复合物(NRC)。分析超速离心和清晰的天然 PAGE 分析表明,NRC 是一种稳定的色素-蛋白复合物,而不是游离 CP47 和 CP43 蛋白的混合物。在暴露于高光和蛋白质合成受损的细胞中,NRC 的含量更高,而 PSII 腔侧的 PsbO 基因缺失会导致 NRC 群体增加,表明 NRC 作为 PSII 修复过程的一部分,是对光损伤的反应而形成的。我们的发现挑战了 PSII 修复循环的当前模型,并暗示了一种替代的 PSII 修复策略。这种复合物的形成可能通过将完整的 PSII 核心天线保存在一个可供 PSII 重新组装的单一复合物中,最大限度地提高 PSII 修复的经济性,从而最小化在光损伤事件后,在类囊体膜中随机稀释多个循环组件的风险。