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对内体回收分选信号的认识不断演变。

An evolving understanding of sorting signals for endosomal retrieval.

作者信息

Yong Xin, Mao Lejiao, Seaman Matthew N J, Jia Da

机构信息

Key Laboratory of Birth Defects and Related Diseases of Women and Children, Department of Paediatrics, West China Second University Hospital, State Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, China.

Cambridge Institute for Medical Research, University of Cambridge, The Keith Peters Building, Cambridge Biomedical Campus, CB2 0XY, UK.

出版信息

iScience. 2022 May 20;25(5):104254. doi: 10.1016/j.isci.2022.104254. Epub 2022 Apr 13.

DOI:10.1016/j.isci.2022.104254
PMID:35434543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9006456/
Abstract

Complex mechanisms govern the sorting of membrane (cargo) proteins at endosomes to ensure that protein localization to the post-Golgi endomembrane system is accurately maintained. Endosomal retrieval complexes mediate sorting by recognizing specific motifs and signals in the cytoplasmic domains of cargo proteins transiting through endosomes. In this review, the recent progress in understanding the molecular mechanisms of how the retromer complex, in conjunction with sorting nexin (SNX) proteins, operates in cargo recognition and sorting is discussed. New data revealing the importance of different SNX proteins and detailing how post-translational modifications can modulate cargo sorting to respond to changes in the environment are highlighted along with the key role that endosomal protein sorting plays in SARS-CoV-2 infection.

摘要

复杂的机制控制着内体中膜(货物)蛋白的分选,以确保蛋白在高尔基体后内膜系统中的定位得以精确维持。内体回收复合体通过识别穿过内体的货物蛋白胞质结构域中的特定基序和信号来介导分选。在本综述中,我们讨论了在理解逆转录复合物与分选连接蛋白(SNX)协同作用于货物识别和分选的分子机制方面的最新进展。同时强调了新数据,这些数据揭示了不同SNX蛋白的重要性,并详细说明了翻译后修饰如何调节货物分选以应对环境变化,以及内体蛋白分选在SARS-CoV-2感染中所起的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd0/9062342/c22ab38118be/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd0/9062342/d969750036af/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd0/9062342/74a160da8e16/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd0/9062342/c22ab38118be/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd0/9062342/d969750036af/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd0/9062342/74a160da8e16/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd0/9062342/c22ab38118be/gr2.jpg

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本文引用的文献

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SNX27-Retromer directly binds ESCPE-1 to transfer cargo proteins during endosomal recycling.SNX27-Retromer 通过直接结合 ESCPE-1 在内涵体循环过程中转运货物蛋白。
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2
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Proc Natl Acad Sci U S A. 2022 Jan 25;119(4). doi: 10.1073/pnas.2117576119.
3
SARS-CoV-2 spike protein harnesses SNX27-mediated endocytic recycling pathway.
Nat Rev Mol Cell Biol. 2024 Oct;25(10):765-783. doi: 10.1038/s41580-024-00746-8. Epub 2024 Jun 17.
4
Emerging Role of Sorting Nexin 17 in Human Health and Disease.分选连接蛋白 17 在人类健康和疾病中的新兴作用。
Curr Protein Pept Sci. 2024;25(10):814-825. doi: 10.2174/0113892037284582240522155112.
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Retromer-mediated recruitment of the WASH complex involves discrete interactions between VPS35, VPS29, and FAM21.Retromer 介导的 WASH 复合物的募集涉及 VPS35、VPS29 和 FAM21 之间的离散相互作用。
Protein Sci. 2024 May;33(5):e4980. doi: 10.1002/pro.4980.
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Structural basis for Retriever-SNX17 assembly and endosomal sorting.Retriever-SNX17组装及内体分选的结构基础
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