Global organelle profiling reveals subcellular localization and remodeling at proteome scale.

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Tác giả: Yttria Aniseia, Rodrigo Baltazar-Nunez, Sophie Bax, James Burgess, Janie R Byrum, Joseph S Creery, Brian C DeFelice, Joshua E Elias, Carlos G Gonzalez, Marco Y Hein, Daniel N Itzhak, Ivan E Ivanov, Camille Januel, Kibeom Kim, Manuel D Leonetti, Chad Liu, Frank McCarthy, Aidan H McMorrow, Shalin B Mehta, Leila Njoya, Duo Peng, Soorya Pradeep, Laura Savy, Madhurya Sekhar, Sara Sunshine, Verina Todorova, Shivanshi Vaid, Madhuri Vangipuram, Eileen Wang, Serena Yeung-Levy

Ngôn ngữ: eng

Ký hiệu phân loại: 523.855 Globular clusters

Thông tin xuất bản: United States : Cell , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 253142

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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