Positional specialization of LIR motifs in RavZ and the autophagy-related protein ATG4B.

Autophagy reports Pub Date : 2024-12-19 eCollection Date: 2025-01-01 DOI:10.1080/27694127.2024.2438563
Sang-Won Park, Jin-A Lee, Deok-Jin Jang
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Abstract

LC3-interacting region (LIR) motifs are essential for recruiting proteins onto autophagosomes, the hallmark of autophagy. We recently explored the relevance of the specific position of the LIRs in RavZ and ATG4B (autophagy-related 4B). RavZ's N-terminal LIRs drive substrate recognition and enzymatic activity, while its C-terminal LIR aids membrane localization. In contrast, ATG4B's C-terminal LIR is indispensable for LC3B (microtubule-associated protein 1 light chain 3B)-phosphatidylethanolamine (PE) delipidation on autophagosomes but not required for cytosolic LC3B priming, which is mediated solely by its catalytic domain (CAD). These findings underscore the structural adaptation of LIRs for context-specific functions. This novel nuanced understanding provides a framework for developing therapeutic tools to modulate autophagy by precisely targeting LIRs or their associated processes, offering potential treatment for diseases like neurodegenerative disorders and infections characterized by autophagy dysregulation.

LIR基序在RavZ和自噬相关蛋白ATG4B中的位置特化。
lc3相互作用区(LIR)基序对于将蛋白质募集到自噬体上是必不可少的,自噬体是自噬的标志。我们最近探索了lir在RavZ和ATG4B(自噬相关4B)中的特定位置的相关性。RavZ的n端LIR驱动底物识别和酶活性,而c端LIR有助于膜定位。相比之下,ATG4B的c端LIR对于LC3B(微管相关蛋白1轻链3B)-磷脂酰乙醇胺(PE)在自噬体上的脱除是必不可少的,但对于仅由其催化结构域(CAD)介导的胞质LC3B启动则不是必需的。这些发现强调了lir对上下文特定功能的结构适应性。这种新颖细致的理解为开发治疗工具提供了一个框架,通过精确靶向lir或其相关过程来调节自噬,为神经退行性疾病和以自噬失调为特征的感染等疾病提供潜在的治疗方法。
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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