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一种通过自噬确保非选择性细胞质降解的机制。

A mechanism that ensures non-selective cytoplasm degradation by autophagy.

机构信息

Cell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, 226-8501, Japan.

Department of Biosystems Science, Institute for Life and Medical Sciences, Kyoto University, Sakyo-ku, Kyoto, 606-8507, Japan.

出版信息

Nat Commun. 2023 Sep 19;14(1):5815. doi: 10.1038/s41467-023-41525-x.

Abstract

In autophagy, a membrane cisterna called the isolation membrane expands, bends, becomes spherical, and closes to sequester cytoplasmic constituents into the resulting double-membrane vesicle autophagosome for lysosomal/vacuolar degradation. Here, we discover a mechanism that allows the isolation membrane to expand with a large opening to ensure non-selective cytoplasm sequestration within the autophagosome. A sorting nexin complex that localizes to the opening edge of the isolation membrane plays a critical role in this process. Without the complex, the isolation membrane expands with a small opening that prevents the entry of particles larger than about 25 nm, including ribosomes and proteasomes, although autophagosomes of nearly normal size eventually form. This study sheds light on membrane morphogenesis during autophagosome formation and selectivity in autophagic degradation.

摘要

在自噬中,一种称为隔离膜的膜质囊泡会扩张、弯曲、变成球形,并闭合将细胞质成分隔离到双层膜囊泡自噬体中,进行溶酶体/液泡降解。在这里,我们发现了一种机制,该机制允许隔离膜扩张形成大开口,以确保自噬体中非选择性细胞质的隔离。定位于隔离膜开口边缘的分选连接蛋白复合物在这个过程中起着关键作用。如果没有该复合物,隔离膜的开口就会很小,阻止直径大于约 25nm 的颗粒进入,包括核糖体和蛋白酶体,尽管最终仍会形成大小接近正常的自噬体。这项研究揭示了自噬体形成过程中膜形态发生和自噬性降解中的选择性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d7/10509180/d9abce2fdad6/41467_2023_41525_Fig1_HTML.jpg

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