Proteomic mapping of cytosol-facing outer mitochondrial and ER membranes in living human cells by proximity biotinylation

Bibliographic Details
Title: Proteomic mapping of cytosol-facing outer mitochondrial and ER membranes in living human cells by proximity biotinylation
Authors: Victoria Hung, Stephanie S Lam, Namrata D Udeshi, Tanya Svinkina, Gaelen Guzman, Vamsi K Mootha, Steven A Carr, Alice Y Ting
Source: eLife, Vol 6 (2017)
Publisher Information: eLife Sciences Publications Ltd, 2017.
Publication Year: 2017
Collection: LCC:Medicine
LCC:Science
LCC:Biology (General)
Subject Terms: microscopy, promiscuous enzymatic labeling, subcellular regions, APEX2, mitochondria-ER junctions, mitochondria-associated membrane, Medicine, Science, Biology (General), QH301-705.5
More Details: The cytosol-facing membranes of cellular organelles contain proteins that enable signal transduction, regulation of morphology and trafficking, protein import and export, and other specialized processes. Discovery of these proteins by traditional biochemical fractionation can be plagued with contaminants and loss of key components. Using peroxidase-mediated proximity biotinylation, we captured and identified endogenous proteins on the outer mitochondrial membrane (OMM) and endoplasmic reticulum membrane (ERM) of living human fibroblasts. The proteomes of 137 and 634 proteins, respectively, are highly specific and highlight 94 potentially novel mitochondrial or ER proteins. Dataset intersection identified protein candidates potentially localized to mitochondria-ER contact sites. We found that one candidate, the tail-anchored, PDZ-domain-containing OMM protein SYNJ2BP, dramatically increases mitochondrial contacts with rough ER when overexpressed. Immunoprecipitation-mass spectrometry identified ribosome-binding protein 1 (RRBP1) as SYNJ2BP’s ERM binding partner. Our results highlight the power of proximity biotinylation to yield insights into the molecular composition and function of intracellular membranes.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2050-084X
Relation: https://elifesciences.org/articles/24463; https://doaj.org/toc/2050-084X
DOI: 10.7554/eLife.24463
Access URL: https://doaj.org/article/3c04e0d0fea24685aae4dc58868f4272
Accession Number: edsdoj.3c04e0d0fea24685aae4dc58868f4272
Database: Directory of Open Access Journals
More Details
ISSN:2050084X
DOI:10.7554/eLife.24463
Published in:eLife
Language:English