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Systematic protein–protein interaction mapping for clinically relevant human GPCRs
G‐protein‐coupled receptors (GPCRs) are the largest family of integral membrane receptors with key roles in regulating signaling pathways targeted by therapeutics, but are difficult to study using existing proteomics technologies due to their complex biochemical features. To obtain a global view of...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371730/ https://www.ncbi.nlm.nih.gov/pubmed/28298427 http://dx.doi.org/10.15252/msb.20167430 |
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author | Sokolina, Kate Kittanakom, Saranya Snider, Jamie Kotlyar, Max Maurice, Pascal Gandía, Jorge Benleulmi‐Chaachoua, Abla Tadagaki, Kenjiro Oishi, Atsuro Wong, Victoria Malty, Ramy H Deineko, Viktor Aoki, Hiroyuki Amin, Shahreen Yao, Zhong Morató, Xavier Otasek, David Kobayashi, Hiroyuki Menendez, Javier Auerbach, Daniel Angers, Stephane Pržulj, Natasa Bouvier, Michel Babu, Mohan Ciruela, Francisco Jockers, Ralf Jurisica, Igor Stagljar, Igor |
author_facet | Sokolina, Kate Kittanakom, Saranya Snider, Jamie Kotlyar, Max Maurice, Pascal Gandía, Jorge Benleulmi‐Chaachoua, Abla Tadagaki, Kenjiro Oishi, Atsuro Wong, Victoria Malty, Ramy H Deineko, Viktor Aoki, Hiroyuki Amin, Shahreen Yao, Zhong Morató, Xavier Otasek, David Kobayashi, Hiroyuki Menendez, Javier Auerbach, Daniel Angers, Stephane Pržulj, Natasa Bouvier, Michel Babu, Mohan Ciruela, Francisco Jockers, Ralf Jurisica, Igor Stagljar, Igor |
author_sort | Sokolina, Kate |
collection | PubMed |
description | G‐protein‐coupled receptors (GPCRs) are the largest family of integral membrane receptors with key roles in regulating signaling pathways targeted by therapeutics, but are difficult to study using existing proteomics technologies due to their complex biochemical features. To obtain a global view of GPCR‐mediated signaling and to identify novel components of their pathways, we used a modified membrane yeast two‐hybrid (MYTH) approach and identified interacting partners for 48 selected full‐length human ligand‐unoccupied GPCRs in their native membrane environment. The resulting GPCR interactome connects 686 proteins by 987 unique interactions, including 299 membrane proteins involved in a diverse range of cellular functions. To demonstrate the biological relevance of the GPCR interactome, we validated novel interactions of the GPR37, serotonin 5‐HT4d, and adenosine ADORA2A receptors. Our data represent the first large‐scale interactome mapping for human GPCRs and provide a valuable resource for the analysis of signaling pathways involving this druggable family of integral membrane proteins. |
format | Online Article Text |
id | pubmed-5371730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53717302017-03-30 Systematic protein–protein interaction mapping for clinically relevant human GPCRs Sokolina, Kate Kittanakom, Saranya Snider, Jamie Kotlyar, Max Maurice, Pascal Gandía, Jorge Benleulmi‐Chaachoua, Abla Tadagaki, Kenjiro Oishi, Atsuro Wong, Victoria Malty, Ramy H Deineko, Viktor Aoki, Hiroyuki Amin, Shahreen Yao, Zhong Morató, Xavier Otasek, David Kobayashi, Hiroyuki Menendez, Javier Auerbach, Daniel Angers, Stephane Pržulj, Natasa Bouvier, Michel Babu, Mohan Ciruela, Francisco Jockers, Ralf Jurisica, Igor Stagljar, Igor Mol Syst Biol Articles G‐protein‐coupled receptors (GPCRs) are the largest family of integral membrane receptors with key roles in regulating signaling pathways targeted by therapeutics, but are difficult to study using existing proteomics technologies due to their complex biochemical features. To obtain a global view of GPCR‐mediated signaling and to identify novel components of their pathways, we used a modified membrane yeast two‐hybrid (MYTH) approach and identified interacting partners for 48 selected full‐length human ligand‐unoccupied GPCRs in their native membrane environment. The resulting GPCR interactome connects 686 proteins by 987 unique interactions, including 299 membrane proteins involved in a diverse range of cellular functions. To demonstrate the biological relevance of the GPCR interactome, we validated novel interactions of the GPR37, serotonin 5‐HT4d, and adenosine ADORA2A receptors. Our data represent the first large‐scale interactome mapping for human GPCRs and provide a valuable resource for the analysis of signaling pathways involving this druggable family of integral membrane proteins. John Wiley and Sons Inc. 2017-03-15 /pmc/articles/PMC5371730/ /pubmed/28298427 http://dx.doi.org/10.15252/msb.20167430 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Sokolina, Kate Kittanakom, Saranya Snider, Jamie Kotlyar, Max Maurice, Pascal Gandía, Jorge Benleulmi‐Chaachoua, Abla Tadagaki, Kenjiro Oishi, Atsuro Wong, Victoria Malty, Ramy H Deineko, Viktor Aoki, Hiroyuki Amin, Shahreen Yao, Zhong Morató, Xavier Otasek, David Kobayashi, Hiroyuki Menendez, Javier Auerbach, Daniel Angers, Stephane Pržulj, Natasa Bouvier, Michel Babu, Mohan Ciruela, Francisco Jockers, Ralf Jurisica, Igor Stagljar, Igor Systematic protein–protein interaction mapping for clinically relevant human GPCRs |
title | Systematic protein–protein interaction mapping for clinically relevant human GPCRs |
title_full | Systematic protein–protein interaction mapping for clinically relevant human GPCRs |
title_fullStr | Systematic protein–protein interaction mapping for clinically relevant human GPCRs |
title_full_unstemmed | Systematic protein–protein interaction mapping for clinically relevant human GPCRs |
title_short | Systematic protein–protein interaction mapping for clinically relevant human GPCRs |
title_sort | systematic protein–protein interaction mapping for clinically relevant human gpcrs |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371730/ https://www.ncbi.nlm.nih.gov/pubmed/28298427 http://dx.doi.org/10.15252/msb.20167430 |
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