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- Publisher Website: 10.1073/pnas.2319060121
- Scopus: eid_2-s2.0-85193530059
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Article: MACSPI enables tissue-selective proteomic and interactomic analyses in multicellular organisms
Title | MACSPI enables tissue-selective proteomic and interactomic analyses in multicellular organisms |
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Authors | |
Keywords | C. elegans chemical biology interactomics protein interaction networks tissue differentiation |
Issue Date | 16-May-2024 |
Publisher | National Academy of Sciences |
Citation | Proceedings of the National Academy of Sciences, 2024, v. 121, n. 21 How to Cite? |
Abstract | Multicellular organisms are composed of many tissue types that have distinct morphologies and functions, which are largely driven by specialized proteomes and interactomes. To define the proteome and interactome of a specific type of tissue in an intact animal, we developed a localized proteomics approach called Methionine Analog-based Cell-Specific Proteomics and Interactomics (MACSPI). This method uses the tissue-specific expression of an engineered methionyl-tRNA synthetase to label proteins with a bifunctional amino acid 2-amino-5-diazirinylnonynoic acid in selected cells. We applied MACSPI in Caenorhabditis elegans, a model multicellular organism, to selectively label, capture, and profile the proteomes of the body wall muscle and the nervous system, which led to the identification of tissue-specific proteins. Using the photo-cross-linker, we successfully profiled HSP90 interactors in muscles and neurons and identified tissue-specific interactors and stress-related interactors. Our study demonstrates that MACSPI can be used to profile tissue-specific proteomes and interactomes in intact multicellular organisms. |
Persistent Identifier | http://hdl.handle.net/10722/344026 |
ISSN | 2023 Impact Factor: 9.4 2023 SCImago Journal Rankings: 3.737 |
DC Field | Value | Language |
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dc.contributor.author | Huang, Siyue | - |
dc.contributor.author | Ran, Qiao | - |
dc.contributor.author | Li, Xiao-Meng | - |
dc.contributor.author | Bao, Xiucong | - |
dc.contributor.author | Zheng, Chaogu | - |
dc.contributor.author | Li, Xiang David | - |
dc.date.accessioned | 2024-06-25T03:29:58Z | - |
dc.date.available | 2024-06-25T03:29:58Z | - |
dc.date.issued | 2024-05-16 | - |
dc.identifier.citation | Proceedings of the National Academy of Sciences, 2024, v. 121, n. 21 | - |
dc.identifier.issn | 0027-8424 | - |
dc.identifier.uri | http://hdl.handle.net/10722/344026 | - |
dc.description.abstract | <p>Multicellular organisms are composed of many tissue types that have distinct morphologies and functions, which are largely driven by specialized proteomes and interactomes. To define the proteome and interactome of a specific type of tissue in an intact animal, we developed a localized proteomics approach called Methionine Analog-based Cell-Specific Proteomics and Interactomics (MACSPI). This method uses the tissue-specific expression of an engineered methionyl-tRNA synthetase to label proteins with a bifunctional amino acid 2-amino-5-diazirinylnonynoic acid in selected cells. We applied MACSPI in <em>Caenorhabditis elegans,</em> a model multicellular organism, to selectively label, capture, and profile the proteomes of the body wall muscle and the nervous system, which led to the identification of tissue-specific proteins. Using the photo-cross-linker, we successfully profiled HSP90 interactors in muscles and neurons and identified tissue-specific interactors and stress-related interactors. Our study demonstrates that MACSPI can be used to profile tissue-specific proteomes and interactomes in intact multicellular organisms.</p> | - |
dc.language | eng | - |
dc.publisher | National Academy of Sciences | - |
dc.relation.ispartof | Proceedings of the National Academy of Sciences | - |
dc.subject | C. elegans | - |
dc.subject | chemical biology | - |
dc.subject | interactomics | - |
dc.subject | protein interaction networks | - |
dc.subject | tissue differentiation | - |
dc.title | MACSPI enables tissue-selective proteomic and interactomic analyses in multicellular organisms | - |
dc.type | Article | - |
dc.identifier.doi | 10.1073/pnas.2319060121 | - |
dc.identifier.scopus | eid_2-s2.0-85193530059 | - |
dc.identifier.volume | 121 | - |
dc.identifier.issue | 21 | - |
dc.identifier.eissn | 1091-6490 | - |
dc.identifier.issnl | 0027-8424 | - |