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ClpX 相互作用组分析揭示了其在蓝藻代谢和光合作用中的调节作用。

Interactome Analysis of ClpX Reveals Its Regulatory Role in Metabolism and Photosynthesis in Cyanobacteria.

机构信息

School of Animal Science and Nutritional Engineering, Wuhan Polytechnic University, Wuhan 430023, China.

State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.

出版信息

J Proteome Res. 2024 Apr 5;23(4):1174-1187. doi: 10.1021/acs.jproteome.3c00610. Epub 2024 Mar 1.

Abstract

Protein homeostasis is essential for cyanobacteria to maintain proper cellular function under adverse and fluctuating conditions. The AAA+ superfamily of proteolytic complexes in cyanobacteria plays a critical role in this process, including ClpXP, which comprises a hexameric ATPase ClpX and a tetradecameric peptidase ClpP. Despite the physiological effects of ClpX on growth and photosynthesis, its potential substrates and underlying mechanisms in cyanobacteria remain unknown. In this study, we employed a streptavidin-biotin affinity pull-down assay coupled with label-free proteome quantitation to analyze the interactome of ClpX in the model cyanobacterium sp. PCC 6803 (hereafter ). We identified 503 proteins as potential ClpX-binding targets, many of which had novel interactions. These ClpX-binding targets were found to be involved in various biological processes, with particular enrichment in metabolic processes and photosynthesis. Using protein-protein docking, GST pull-down, and biolayer interferometry assays, we confirmed the direct association of ClpX with the photosynthetic proteins, ferredoxin-NADP oxidoreductase (FNR) and phycocyanin subunit (CpcA). Subsequent functional investigations revealed that ClpX participates in the maintenance of FNR homeostasis and functionality in grown under different light conditions. Overall, our study provides a comprehensive understanding of the extensive functions regulated by ClpX in cyanobacteria to maintain protein homeostasis and adapt to environmental challenges.

摘要

蛋白质动态平衡对于蓝藻在不利和波动的条件下维持正常的细胞功能至关重要。蓝藻中的 AAA+ 超家族蛋白酶体复合物在这个过程中起着关键作用,其中包括 ClpXP,它由六聚体 ATP 酶 ClpX 和十四聚体肽酶 ClpP 组成。尽管 ClpX 对生长和光合作用有生理影响,但它在蓝藻中的潜在底物和潜在机制仍不清楚。在这项研究中,我们采用链霉亲和素-生物素亲和下拉测定法结合无标记蛋白质组定量分析来分析模型蓝藻 sp. PCC 6803(以下简称 )中 ClpX 的相互作用组。我们鉴定了 503 种可能与 ClpX 结合的蛋白质,其中许多具有新的相互作用。这些 ClpX 结合靶标被发现参与各种生物学过程,特别是在代谢过程和光合作用中富集。通过蛋白质-蛋白质对接、GST 下拉和生物层干涉测定,我们证实了 ClpX 与光合作用蛋白 ferredoxin-NADP 氧化还原酶(FNR)和藻蓝蛋白亚基(CpcA)的直接结合。随后的功能研究表明,ClpX 参与了 FNR 在家养条件下的动态平衡和功能的维持不同光照条件。总的来说,我们的研究提供了对 ClpX 在蓝藻中调节的广泛功能的全面理解,以维持蛋白质动态平衡和适应环境挑战。

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