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)), Madhurya Sekhar(Chan Zuckerberg Initiative (United States)), Shivanshi Vaid(Chan Zuckerberg Initiative (United States)), Sophie Bax(Chan Zuckerberg Initiative (United States)), Madhuri Vangipuram(Chan Zuckerberg Initiative (United States)), James Burgess(Stanford University), Leila Njoya(Chan Zuckerberg Initiative (United States)), Eileen Wang(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)), Joseph S. Creery(Chan Zuckerberg Initiative (United States)), Aidan H. McMorrow(Chan Zuckerberg Initiative (United States)), 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(Chan Zuckerberg Initiative (United States)), Joshua E. Elias(Chan Zuckerberg Initiative (United States)), Manuel D. Leonetti(Chan Zuckerberg Initiative (United States))
Cell
December 31, 2024
Cited by 77Open Access
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Abstract

Defining the subcellular distribution of all human proteins and their remodeling across cellular states remains a central goal in cell biology. Here, we present a high-resolution strategy to map subcellular organization using organelle immunocapture coupled to mass spectrometry. We apply this workflow to a cell-wide collection of membranous and membraneless compartments. A graph-based analysis assigns the subcellular localization of over 7,600 proteins, defines spatial networks, and uncovers interconnections between cellular compartments. 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 abundance. Our results establish that proteome-wide analysis of subcellular remodeling provides key insights for elucidating cellular responses, uncovering an essential role for ferroptosis in OC43 infection. Our dataset can be explored at organelles.czbiohub.org.


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