File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)

Article: MACSPI enables tissue-selective proteomic and interactomic analyses in multicellular organisms

TitleMACSPI enables tissue-selective proteomic and interactomic analyses in multicellular organisms
Authors
KeywordsC. elegans
chemical biology
interactomics
protein interaction networks
tissue differentiation
Issue Date16-May-2024
PublisherNational 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 Identifierhttp://hdl.handle.net/10722/344026
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.737

 

DC FieldValueLanguage
dc.contributor.authorHuang, Siyue-
dc.contributor.authorRan, Qiao-
dc.contributor.authorLi, Xiao-Meng-
dc.contributor.authorBao, Xiucong-
dc.contributor.authorZheng, Chaogu-
dc.contributor.authorLi, Xiang David-
dc.date.accessioned2024-06-25T03:29:58Z-
dc.date.available2024-06-25T03:29:58Z-
dc.date.issued2024-05-16-
dc.identifier.citationProceedings of the National Academy of Sciences, 2024, v. 121, n. 21-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://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.languageeng-
dc.publisherNational Academy of Sciences-
dc.relation.ispartofProceedings of the National Academy of Sciences-
dc.subjectC. elegans-
dc.subjectchemical biology-
dc.subjectinteractomics-
dc.subjectprotein interaction networks-
dc.subjecttissue differentiation-
dc.titleMACSPI enables tissue-selective proteomic and interactomic analyses in multicellular organisms-
dc.typeArticle-
dc.identifier.doi10.1073/pnas.2319060121-
dc.identifier.scopuseid_2-s2.0-85193530059-
dc.identifier.volume121-
dc.identifier.issue21-
dc.identifier.eissn1091-6490-
dc.identifier.issnl0027-8424-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats