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Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies
Recent years have seen major advances in the structural understanding of the different components of tripartite efflux assemblies, which encompass the multidrug efflux (MDR) pumps and type I secretion systems. The majority of these investigations have focused on the role played by the inner membrane tra...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446572/ https://www.ncbi.nlm.nih.gov/pubmed/26074901 http://dx.doi.org/10.3389/fmicb.2015.00513 |
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author | Symmons, Martyn F. Marshall, Robert L. Bavro, Vassiliy N. |
author_facet | Symmons, Martyn F. Marshall, Robert L. Bavro, Vassiliy N. |
author_sort | Symmons, Martyn F. |
collection | PubMed |
description | Recent years have seen major advances in the structural understanding of the different components of tripartite efflux assemblies, which encompass the multidrug efflux (MDR) pumps and type I secretion systems. The majority of these investigations have focused on the role played by the inner membrane transporters and the outer membrane factor (OMF), leaving the third component of the system – the Periplasmic Adaptor Proteins (PAPs) – relatively understudied. Here we review the current state of knowledge of these versatile proteins which, far from being passive linkers between the OMF and the transporter, emerge as active architects of tripartite assemblies, and play diverse roles in the transport process. Recognition between the PAPs and OMFs is essential for pump assembly and function, and targeting this interaction may provide a novel avenue for combating multidrug resistance. With the recent advances elucidating the drug efflux and energetics of the tripartite assemblies, the understanding of the interaction between the OMFs and PAPs is the last piece remaining in the complete structure of the tripartite pump assembly puzzle. |
format | Online Article Text |
id | pubmed-4446572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44465722015-06-12 Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies Symmons, Martyn F. Marshall, Robert L. Bavro, Vassiliy N. Front Microbiol Microbiology Recent years have seen major advances in the structural understanding of the different components of tripartite efflux assemblies, which encompass the multidrug efflux (MDR) pumps and type I secretion systems. The majority of these investigations have focused on the role played by the inner membrane transporters and the outer membrane factor (OMF), leaving the third component of the system – the Periplasmic Adaptor Proteins (PAPs) – relatively understudied. Here we review the current state of knowledge of these versatile proteins which, far from being passive linkers between the OMF and the transporter, emerge as active architects of tripartite assemblies, and play diverse roles in the transport process. Recognition between the PAPs and OMFs is essential for pump assembly and function, and targeting this interaction may provide a novel avenue for combating multidrug resistance. With the recent advances elucidating the drug efflux and energetics of the tripartite assemblies, the understanding of the interaction between the OMFs and PAPs is the last piece remaining in the complete structure of the tripartite pump assembly puzzle. Frontiers Media S.A. 2015-05-28 /pmc/articles/PMC4446572/ /pubmed/26074901 http://dx.doi.org/10.3389/fmicb.2015.00513 Text en Copyright © 2015 Symmons, Marshall and Bavro. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Symmons, Martyn F. Marshall, Robert L. Bavro, Vassiliy N. Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies |
title | Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies |
title_full | Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies |
title_fullStr | Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies |
title_full_unstemmed | Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies |
title_short | Architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies |
title_sort | architecture and roles of periplasmic adaptor proteins in tripartite efflux assemblies |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446572/ https://www.ncbi.nlm.nih.gov/pubmed/26074901 http://dx.doi.org/10.3389/fmicb.2015.00513 |
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