自噬体-溶酶体融合机制的分子结构和功能。

Autophagy reports Pub Date : 2024-01-01 Epub Date: 2024-02-04 DOI:10.1080/27694127.2024.2305594
Jiajie Diao, Calvin K Yip, Qing Zhong
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引用次数: 0

摘要

大自噬(又称自噬)在维持细胞平衡方面发挥着关键作用。多步骤自噬降解途径的终极步骤涉及载货的双膜自噬体与溶酶体/囊泡之间的融合。在过去的十年中,执行这一关键的终端自噬事件的分子机制的各种核心成分已被确定。这篇综述重点介绍了最近在了解这一高度复杂的机制的主要成分的分子结构、生化功能和调控机制方面取得的进展,这些成分包括 SNARE fusogens、系留因子、Rab GTPases 和相关的鸟嘌呤核苷酸交换因子以及其他附属因子。
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Molecular structures and function of the autophagosome-lysosome fusion machinery.

Macroautophagy (also known as autophagy) plays a pivotal role in maintaining cellular homeostasis. The terminal step of the multi-step autophagy degradation pathway involves fusion between the cargo-laden, double-membraned autophagosome and the lytic organelle lysosome/vacuole. Over the past decade, various core components of the molecular machinery that execute this critical terminal autophagy event have been identified. This review highlights recent advances in understanding the molecular structures, biochemical functions, and regulatory mechanisms of key components of this highly sophisticated machinery including the SNARE fusogens, tethering factors, Rab GTPases and associated guanine nucleotide exchange factors, and other accessory factors.

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