Regulation of autophagy by protein lipidation.

Yuqian Shao, Junchao Hu, Huihui Li, Kefeng Lu
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Abstract

Autophagy is a conserved catabolic recycling pathway that can eliminate cytosolic materials to maintain homeostasis and organelle functions. Many studies over the past few decades have demonstrated that abnormal autophagy is associated with a variety of diseases. Protein lipidation plays an important role in the regulation of autophagy by affecting protein trafficking, localization, stability, interactions and signal transduction. Here, we review recent advances in the understanding of the role of lipidation in autophagy, including S-palmitoylation, N-myristoylation, S-prenylation, glycosylphosphatidylinositol (GPI) anchor modification and cholesterylation. We comprehensively review the enzymes and catalytic mechanisms of lipidation and discuss the relationship between lipidation and autophagy, aiming to deepen the understanding of lipidation and promote the discovery of drug targets for the treatment of autophagy-related diseases.

蛋白脂化对自噬的调节。
自噬是一种保守的分解代谢循环途径,可以消除细胞内物质以维持体内平衡和细胞器功能。过去几十年的许多研究表明,异常自噬与多种疾病有关。蛋白质脂化通过影响蛋白质的转运、定位、稳定性、相互作用和信号转导,在自噬调控中发挥重要作用。在此,我们回顾了近年来关于脂化在自噬中的作用的研究进展,包括s -棕榈酰化、n -肉豆蔻酰化、s -戊烯酰化、糖基磷脂酰肌醇(GPI)锚定修饰和胆固醇化。我们全面综述了脂化的酶和催化机制,探讨了脂化与自噬的关系,旨在加深对脂化的认识,促进发现治疗自噬相关疾病的药物靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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