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条件性蛋白质功能通过应激生理学中的 N-降解途径介导的蛋白质稳态实现。

Conditional Protein Function via N-Degron Pathway-Mediated Proteostasis in Stress Physiology.

机构信息

Independent Junior Research Group on Protein Recognition and Degradation, Leibniz Institute of Plant Biochemistry (IPB) and ScienceCampus Halle-Plant-Based Bioeconomy, D-06120 Halle (Saale), Germany; email:

出版信息

Annu Rev Plant Biol. 2019 Apr 29;70:83-117. doi: 10.1146/annurev-arplant-050718-095937. Epub 2019 Mar 20.

Abstract

The N-degron pathway, formerly the N-end rule pathway, regulates functions of regulatory proteins. It impacts protein half-life and therefore directs the actual presence of target proteins in the cell. The current concept holds that the N-degron pathway depends on the identity of the amino (N)-terminal amino acid and many other factors, such as the follow-up sequence at the N terminus, conformation, flexibility, and protein localization. It is evolutionarily conserved throughout the kingdoms. One possible entry point for substrates of the N-degron pathway is oxidation of N-terminal Cys residues. Oxidation of N-terminal Cys is decisive for further enzymatic modification of various neo-N termini by arginylation that generates potentially neofunctionalized or instable proteoforms. Here, I focus on the posttranslational modifications that are encompassed by protein degradation via the Cys/Arg branch of the N-degron pathway-part of the PROTEOLYSIS 6 (PRT6)/N-degron pathway-as well as the underlying physiological principles of this branch and its biological significance in stress response.

摘要

N-连接肽降解途径,以前称为 N 端规则途径,调节调节蛋白的功能。它影响蛋白质的半衰期,因此决定了靶蛋白在细胞中的实际存在。目前的概念认为,N-连接肽降解途径取决于氨基(N)末端氨基酸的身份和许多其他因素,例如 N 末端的后续序列、构象、灵活性和蛋白质定位。它在整个生物界中是进化保守的。N-连接肽降解途径底物的一个可能进入点是 N 端 Cys 残基的氧化。N 端 Cys 的氧化对于通过精氨酸化进一步酶修饰各种新 N 端至关重要,精氨酸化生成潜在功能化或不稳定的蛋白异构体。在这里,我重点介绍通过 Cys/Arg 分支的蛋白质降解所包含的翻译后修饰,该分支是 PROTEOLYSIS 6(PRT6)/N-连接肽降解途径的一部分,以及该分支的潜在生理原理及其在应激反应中的生物学意义。

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