首页    期刊浏览 2024年12月12日 星期四
登录注册

文章基本信息

  • 标题:Split-TurboID enables contact-dependent proximity labeling in cells
  • 本地全文:下载
  • 作者:Kelvin F. Cho ; Tess C. Branon ; Sanjana Rajeev
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2020
  • 卷号:117
  • 期号:22
  • 页码:12143-12154
  • DOI:10.1073/pnas.1919528117
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Proximity labeling catalyzed by promiscuous enzymes, such as TurboID, have enabled the proteomic analysis of subcellular regions difficult or impossible to access by conventional fractionation-based approaches. Yet some cellular regions, such as organelle contact sites, remain out of reach for current PL methods. To address this limitation, we split the enzyme TurboID into two inactive fragments that recombine when driven together by a protein–protein interaction or membrane–membrane apposition. At endoplasmic reticulum–mitochondria contact sites, reconstituted TurboID catalyzed spatially restricted biotinylation, enabling the enrichment and identification of >100 endogenous proteins, including many not previously linked to endoplasmic reticulum–mitochondria contacts. We validated eight candidates by biochemical fractionation and overexpression imaging. Overall, split-TurboID is a versatile tool for conditional and spatially specific proximity labeling in cells.
  • 关键词:proximity labeling ; ER–mitochondria contacts ; split-TurboID
国家哲学社会科学文献中心版权所有