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Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay
Various repertoires of membrane protein interactions determine cellular responses to diverse environments around cells dynamically in space and time. Current assays, however, have limitations in unraveling these interactions in the physiological states in a living cell due to the lack of capability...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080847/ https://www.ncbi.nlm.nih.gov/pubmed/33603128 http://dx.doi.org/10.1038/s12276-021-00567-1 |
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author | Jeong, Min Gyu Zhou, Kai Park, Soyeon An, HyeongJeon Kwon, Yonghoon Chang, Yeonho Kim, Do-Hyeon Ryu, Sung Ho |
author_facet | Jeong, Min Gyu Zhou, Kai Park, Soyeon An, HyeongJeon Kwon, Yonghoon Chang, Yeonho Kim, Do-Hyeon Ryu, Sung Ho |
author_sort | Jeong, Min Gyu |
collection | PubMed |
description | Various repertoires of membrane protein interactions determine cellular responses to diverse environments around cells dynamically in space and time. Current assays, however, have limitations in unraveling these interactions in the physiological states in a living cell due to the lack of capability to probe the transient nature of these interactions on the crowded membrane. Here, we present a simple and robust assay that enables the investigation of transient protein interactions in living cells by using the single-molecule diffusional mobility shift assay (smDIMSA). Utilizing smDIMSA, we uncovered the interaction profile of EGFR with various membrane proteins and demonstrated the promiscuity of these interactions depending on the cancer cell line. The transient interaction profile obtained by smDIMSA will provide critical information to comprehend the crosstalk among various receptors on the plasma membrane. |
format | Online Article Text |
id | pubmed-8080847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80808472021-04-29 Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay Jeong, Min Gyu Zhou, Kai Park, Soyeon An, HyeongJeon Kwon, Yonghoon Chang, Yeonho Kim, Do-Hyeon Ryu, Sung Ho Exp Mol Med Article Various repertoires of membrane protein interactions determine cellular responses to diverse environments around cells dynamically in space and time. Current assays, however, have limitations in unraveling these interactions in the physiological states in a living cell due to the lack of capability to probe the transient nature of these interactions on the crowded membrane. Here, we present a simple and robust assay that enables the investigation of transient protein interactions in living cells by using the single-molecule diffusional mobility shift assay (smDIMSA). Utilizing smDIMSA, we uncovered the interaction profile of EGFR with various membrane proteins and demonstrated the promiscuity of these interactions depending on the cancer cell line. The transient interaction profile obtained by smDIMSA will provide critical information to comprehend the crosstalk among various receptors on the plasma membrane. Nature Publishing Group UK 2021-02-19 /pmc/articles/PMC8080847/ /pubmed/33603128 http://dx.doi.org/10.1038/s12276-021-00567-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jeong, Min Gyu Zhou, Kai Park, Soyeon An, HyeongJeon Kwon, Yonghoon Chang, Yeonho Kim, Do-Hyeon Ryu, Sung Ho Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay |
title | Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay |
title_full | Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay |
title_fullStr | Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay |
title_full_unstemmed | Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay |
title_short | Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay |
title_sort | analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080847/ https://www.ncbi.nlm.nih.gov/pubmed/33603128 http://dx.doi.org/10.1038/s12276-021-00567-1 |
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