The Erv41-Erv46 complex serves as a retrograde receptor to retrieve misfolded secretory proteins that have escaped from the ER.

IF 2.7 3区 生物学 Q3 CELL BIOLOGY
Molecular Biology of the Cell Pub Date : 2025-07-01 Epub Date: 2025-05-06 DOI:10.1091/mbc.E25-02-0090
John A Fuesler, Jaime R Blais, Charles Barlowe
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引用次数: 0

Abstract

The Erv41-Erv46 complex is a conserved transmembrane cargo receptor that returns endoplasmic reticulum (ER)-resident proteins that have reached the Golgi complex back to the ER. Here, we report that this retrograde receptor also retrieves misfolded secretory cargo that contain luminal domain lesions, such as CPY*. Cells lacking Erv41-Erv46, increase the cellular clearance of misfolded cargo proteins due to increased ER escape and transport to the cell surface or to the vacuole for degradation. Erv41-Erv46 displays selectivity in binding misfolded substrates compared with their folded counterparts. Binding experiments reconstituted with purified proteins demonstrate that Erv41-Erv46 complex binds directly to misfolded CPY* through a shared cargo-binding site. These findings indicate that Erv41-Erv46 acts as a post-ER protein quality control checkpoint and expand the client range by which retrograde receptors ensure delivery of correctly folded secretory proteins.

Erv41-Erv46复合物作为一种逆行受体来检索从内质网逃逸的错误折叠的分泌蛋白。
Erv41-Erv46复合体是一种保守的跨膜货物受体,它将到达高尔基复合体的内质网驻留蛋白返回内质网。在这里,我们报告逆行受体也检索包含管腔结构域病变的错误折叠的分泌货物,如CPY*。缺乏Erv41-Erv46的细胞增加了错误折叠的货物蛋白的细胞清除率,这是由于内质网逃逸和转运到细胞表面或液泡降解的增加。Erv41-Erv46在结合错误折叠底物方面表现出选择性。用纯化蛋白重组的结合实验表明,Erv41-Erv46复合物通过共享的货物结合位点直接与错误折叠的CPY*结合。这些发现表明,Erv41-Erv46作为内质网后蛋白质量控制检查点,扩大了逆行受体确保正确折叠分泌蛋白递送的客户范围。
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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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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