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A survey of integral α-helical membrane proteins
Membrane proteins serve as cellular gatekeepers, regulators, and sensors. Prior studies have explored the functional breadth and evolution of proteins and families of particular interest, such as the diversity of transport-associated membrane protein families in prokaryotes and eukaryotes, the compo...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780624/ https://www.ncbi.nlm.nih.gov/pubmed/19760129 http://dx.doi.org/10.1007/s10969-009-9069-8 |
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author | Kelly, Libusha Pieper, Ursula Eswar, Narayanan Hays, Franklin A. Li, Min Roe-Zurz, Zygy Kroetz, Deanna L. Giacomini, Kathleen M. Stroud, Robert M. Sali, Andrej |
author_facet | Kelly, Libusha Pieper, Ursula Eswar, Narayanan Hays, Franklin A. Li, Min Roe-Zurz, Zygy Kroetz, Deanna L. Giacomini, Kathleen M. Stroud, Robert M. Sali, Andrej |
author_sort | Kelly, Libusha |
collection | PubMed |
description | Membrane proteins serve as cellular gatekeepers, regulators, and sensors. Prior studies have explored the functional breadth and evolution of proteins and families of particular interest, such as the diversity of transport-associated membrane protein families in prokaryotes and eukaryotes, the composition of integral membrane proteins, and family classification of all human G-protein coupled receptors. However, a comprehensive analysis of the content and evolutionary associations between membrane proteins and families in a diverse set of genomes is lacking. Here, a membrane protein annotation pipeline was developed to define the integral membrane genome and associations between 21,379 proteins from 34 genomes; most, but not all of these proteins belong to 598 defined families. The pipeline was used to provide target input for a structural genomics project that successfully cloned, expressed, and purified 61 of our first 96 selected targets in yeast. Furthermore, the methodology was applied (1) to explore the evolutionary history of the substrate-binding transmembrane domains of the human ABC transporter superfamily, (2) to identify the multidrug resistance-associated membrane proteins in whole genomes, and (3) to identify putative new membrane protein families. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10969-009-9069-8) contains supplementary material, which is available to authorized users. |
format | Text |
id | pubmed-2780624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-27806242009-11-23 A survey of integral α-helical membrane proteins Kelly, Libusha Pieper, Ursula Eswar, Narayanan Hays, Franklin A. Li, Min Roe-Zurz, Zygy Kroetz, Deanna L. Giacomini, Kathleen M. Stroud, Robert M. Sali, Andrej J Struct Funct Genomics Article Membrane proteins serve as cellular gatekeepers, regulators, and sensors. Prior studies have explored the functional breadth and evolution of proteins and families of particular interest, such as the diversity of transport-associated membrane protein families in prokaryotes and eukaryotes, the composition of integral membrane proteins, and family classification of all human G-protein coupled receptors. However, a comprehensive analysis of the content and evolutionary associations between membrane proteins and families in a diverse set of genomes is lacking. Here, a membrane protein annotation pipeline was developed to define the integral membrane genome and associations between 21,379 proteins from 34 genomes; most, but not all of these proteins belong to 598 defined families. The pipeline was used to provide target input for a structural genomics project that successfully cloned, expressed, and purified 61 of our first 96 selected targets in yeast. Furthermore, the methodology was applied (1) to explore the evolutionary history of the substrate-binding transmembrane domains of the human ABC transporter superfamily, (2) to identify the multidrug resistance-associated membrane proteins in whole genomes, and (3) to identify putative new membrane protein families. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10969-009-9069-8) contains supplementary material, which is available to authorized users. Springer Netherlands 2009-09-17 2009 /pmc/articles/PMC2780624/ /pubmed/19760129 http://dx.doi.org/10.1007/s10969-009-9069-8 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Article Kelly, Libusha Pieper, Ursula Eswar, Narayanan Hays, Franklin A. Li, Min Roe-Zurz, Zygy Kroetz, Deanna L. Giacomini, Kathleen M. Stroud, Robert M. Sali, Andrej A survey of integral α-helical membrane proteins |
title | A survey of integral α-helical membrane proteins |
title_full | A survey of integral α-helical membrane proteins |
title_fullStr | A survey of integral α-helical membrane proteins |
title_full_unstemmed | A survey of integral α-helical membrane proteins |
title_short | A survey of integral α-helical membrane proteins |
title_sort | survey of integral α-helical membrane proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780624/ https://www.ncbi.nlm.nih.gov/pubmed/19760129 http://dx.doi.org/10.1007/s10969-009-9069-8 |
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