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An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations
Protein-protein interactions govern almost all cellular functions. These complex networks of stable and transient associations can be mapped by affinity purification mass spectrometry (AP-MS) and complementary proximity-based labeling methods such as BioID. To exploit the advantages of both strategi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864832/ https://www.ncbi.nlm.nih.gov/pubmed/29568061 http://dx.doi.org/10.1038/s41467-018-03523-2 |
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author | Liu, Xiaonan Salokas, Kari Tamene, Fitsum Jiu, Yaming Weldatsadik, Rigbe G. Öhman, Tiina Varjosalo, Markku |
author_facet | Liu, Xiaonan Salokas, Kari Tamene, Fitsum Jiu, Yaming Weldatsadik, Rigbe G. Öhman, Tiina Varjosalo, Markku |
author_sort | Liu, Xiaonan |
collection | PubMed |
description | Protein-protein interactions govern almost all cellular functions. These complex networks of stable and transient associations can be mapped by affinity purification mass spectrometry (AP-MS) and complementary proximity-based labeling methods such as BioID. To exploit the advantages of both strategies, we here design and optimize an integrated approach combining AP-MS and BioID in a single construct, which we term MAC-tag. We systematically apply the MAC-tag approach to 18 subcellular and 3 sub-organelle localization markers, generating a molecular context database, which can be used to define a protein’s molecular location. In addition, we show that combining the AP-MS and BioID results makes it possible to obtain interaction distances within a protein complex. Taken together, our integrated strategy enables the comprehensive mapping of the physical and functional interactions of proteins, defining their molecular context and improving our understanding of the cellular interactome. |
format | Online Article Text |
id | pubmed-5864832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58648322018-03-28 An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations Liu, Xiaonan Salokas, Kari Tamene, Fitsum Jiu, Yaming Weldatsadik, Rigbe G. Öhman, Tiina Varjosalo, Markku Nat Commun Article Protein-protein interactions govern almost all cellular functions. These complex networks of stable and transient associations can be mapped by affinity purification mass spectrometry (AP-MS) and complementary proximity-based labeling methods such as BioID. To exploit the advantages of both strategies, we here design and optimize an integrated approach combining AP-MS and BioID in a single construct, which we term MAC-tag. We systematically apply the MAC-tag approach to 18 subcellular and 3 sub-organelle localization markers, generating a molecular context database, which can be used to define a protein’s molecular location. In addition, we show that combining the AP-MS and BioID results makes it possible to obtain interaction distances within a protein complex. Taken together, our integrated strategy enables the comprehensive mapping of the physical and functional interactions of proteins, defining their molecular context and improving our understanding of the cellular interactome. Nature Publishing Group UK 2018-03-22 /pmc/articles/PMC5864832/ /pubmed/29568061 http://dx.doi.org/10.1038/s41467-018-03523-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, Xiaonan Salokas, Kari Tamene, Fitsum Jiu, Yaming Weldatsadik, Rigbe G. Öhman, Tiina Varjosalo, Markku An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations |
title | An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations |
title_full | An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations |
title_fullStr | An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations |
title_full_unstemmed | An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations |
title_short | An AP-MS- and BioID-compatible MAC-tag enables comprehensive mapping of protein interactions and subcellular localizations |
title_sort | ap-ms- and bioid-compatible mac-tag enables comprehensive mapping of protein interactions and subcellular localizations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864832/ https://www.ncbi.nlm.nih.gov/pubmed/29568061 http://dx.doi.org/10.1038/s41467-018-03523-2 |
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