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吞噬泡闭合。

Phagophore Closure.

机构信息

College of Life Sciences, Nanjing Agricultural University, Nanjing, China.

出版信息

Adv Exp Med Biol. 2021;1208:43-53. doi: 10.1007/978-981-16-2830-6_3.

Abstract

Phagophore closure is a critical step during macroautophagy. However, the proteins and mechanisms to regulate this step have been elusive for a long time. In 2017, Rab5 was affirmed to play a role in phagophore closure in yeast. Furthermore, in mammalian cells, ESCRT III was reported to have roles in phagophore closure and mitophagosome closure in vivo in 2018 and 2019, respectively. The role of ESCRT in phagophore closure was confirmed in yeast, both in vivo and in vitro, in 2019. Most importantly, the latter paper found that Atg17 recruited the ESCRT III subunit Snf7 to the phagophore to close it under the control of Rab5. To determine the closure characteristics of autophagosome-like membrane structures in ESCRT mutants, a traditional protease protection assay with immunoblotting was used, accompanied by new techniques that were developed, including immunofluorescence assays, autophagosome completion assays, and the optogenetic closure assay. This study delivered our current understanding of phagophore closure and provided more reference methods to detect membrane closure.

摘要

吞噬体闭合是巨自噬过程中的一个关键步骤。然而,长期以来,调节这一步骤的蛋白质和机制一直难以捉摸。2017 年,Rab5 被证实在酵母中参与吞噬体闭合。此外,在哺乳动物细胞中,ESCRT III 分别于 2018 年和 2019 年被报道在体内参与吞噬体闭合和线粒体自噬体闭合。2019 年,在酵母中,无论是在体内还是在体外,都证实了 ESCRT 在吞噬体闭合中的作用。最重要的是,后一篇论文发现 Atg17 在 Rab5 的控制下将 ESCRT III 亚基 Snf7 招募到吞噬体上以关闭它。为了确定 ESCRT 突变体中类似自噬体的膜结构的闭合特性,使用了传统的蛋白酶保护测定法结合免疫印迹法,并开发了新的技术,包括免疫荧光测定法、自噬体完成测定法和光遗传闭合测定法。本研究提供了我们对吞噬体闭合的当前理解,并提供了更多检测膜闭合的参考方法。

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