Global organelle profiling reveals subcellular localization and remodeling at proteome scale

Marco Y. Hein(Chan Zuckerberg Initiative (United States)), Duo Peng(Chan Zuckerberg Initiative (United States)), Verina Todorova(Chan Zuckerberg Initiative (United States)), Frank McCarthy(Chan Zuckerberg Initiative (United States)), Kibeom Kim(Chan Zuckerberg Initiative (United States)), Chad Liu(Chan Zuckerberg Initiative (United States)), Laura Savy(Chan Zuckerberg Initiative (United States)), Camille Januel(Chan Zuckerberg Initiative (United States)), Rodrigo Baltazar-Nunez(Chan Zuckerberg Initiative (United States)), Sophie Bax(Chan Zuckerberg Initiative (United States)), Shivanshi Vaid(Chan Zuckerberg Initiative (United States)), Madhuri Vangipuram(Chan Zuckerberg Initiative (United States)), Ivan E. Ivanov(Chan Zuckerberg Initiative (United States)), Janie R. Byrum(Chan Zuckerberg Initiative (United States)), Soorya Pradeep(Chan Zuckerberg Initiative (United States)), Carlos G. Gonzalez(Chan Zuckerberg Initiative (United States)), Yttria Aniseia(Chan Zuckerberg Initiative (United States)), Eileen Wang(Chan Zuckerberg Initiative (United States)), Joseph S. Creery(Chan Zuckerberg Initiative (United States)), Aidan H. McMorrow(Chan Zuckerberg Initiative (United States)), James Burgess(Stanford University), Sara Sunshine(University of California, San Francisco), Serena Yeung-Levy(Chan Zuckerberg Initiative (United States)), Brian C. DeFelice(Chan Zuckerberg Initiative (United States)), Shalin B. Mehta(Chan Zuckerberg Initiative (United States)), Daniel N. Itzhak(Bay Institute), Joshua E. Elias(Chan Zuckerberg Initiative (United States)), Manuel D. Leonetti(Chan Zuckerberg Initiative (United States))
bioRxiv (Cold Spring Harbor Laboratory)
December 18, 2023
Cited by 24Open Access
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Abstract

ABSTRACT Defining the subcellular distribution of all human proteins and its remodeling across cellular states remains a central goal in cell biology. Here, we present a high-resolution strategy to map subcellular organization using organelle immuno-capture coupled to mass spectrometry. We apply this proteomics workflow to a cell-wide collection of membranous and membrane-less compartments. A graph-based representation of our data reveals the subcellular localization of over 7,600 proteins, defines spatial protein networks, and uncovers interconnections between cellular compartments. We demonstrate that our approach can be deployed to comprehensively profile proteome remodeling during cellular perturbation. By characterizing the cellular landscape following hCoV-OC43 viral infection, we discover that many proteins are regulated by changes in their spatial distribution rather than by changes in their total abundance. Our results establish that proteome-wide analysis of subcellular remodeling provides essential insights for the elucidation of cellular responses. Our dataset can be explored at organelles.czbiohub.org .


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