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Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3

The multiple transferable resistance (mTR) pump from Neisseria gonorrhoeae MtrCDE multidrug pump is assembled from the inner and outer membrane proteins MtrD and MtrE and the periplasmic membrane fusion protein MtrC. Previously we established that while there is a weak interaction of MtrD and MtrE,...

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Autores principales: Janganan, Thamarai K., Bavro, Vassiliy N., Zhang, Li, Matak-Vinkovic, Dijana, Barrera, Nelson P., Venien-Bryan, Catherine, Robinson, Carol V., Borges-Walmsley, Maria Inês, Walmsley, Adrian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143649/
https://www.ncbi.nlm.nih.gov/pubmed/21610073
http://dx.doi.org/10.1074/jbc.M111.246595
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author Janganan, Thamarai K.
Bavro, Vassiliy N.
Zhang, Li
Matak-Vinkovic, Dijana
Barrera, Nelson P.
Venien-Bryan, Catherine
Robinson, Carol V.
Borges-Walmsley, Maria Inês
Walmsley, Adrian R.
author_facet Janganan, Thamarai K.
Bavro, Vassiliy N.
Zhang, Li
Matak-Vinkovic, Dijana
Barrera, Nelson P.
Venien-Bryan, Catherine
Robinson, Carol V.
Borges-Walmsley, Maria Inês
Walmsley, Adrian R.
author_sort Janganan, Thamarai K.
collection PubMed
description The multiple transferable resistance (mTR) pump from Neisseria gonorrhoeae MtrCDE multidrug pump is assembled from the inner and outer membrane proteins MtrD and MtrE and the periplasmic membrane fusion protein MtrC. Previously we established that while there is a weak interaction of MtrD and MtrE, MtrC binds with relatively high affinity to both MtrD and MtrE. MtrD conferred antibiotic resistance only when it was expressed with MtrE and MtrC, suggesting that these proteins form a functional tripartite complex in which MtrC bridges MtrD and MtrE. Furthermore, we demonstrated that MtrC interacts with an intraprotomer groove on the surface of MtrE, inducing channel opening. However, a second groove is apparent at the interface of the MtrE subunits, which might also be capable of engaging MtrC. We have now established that MtrC can be cross-linked to cysteines placed in this interprotomer groove and that mutation of residues in the groove impair the ability of the pump to confer antibiotic resistance by locking MtrE in the closed channel conformation. Moreover, MtrE K390C forms an intermolecular disulfide bond with MtrC E149C locking MtrE in the open channel conformation, suggesting that a functional salt bridge forms between these residues during the transition from closed to open channel conformations. MtrC forms dimers that assemble into hexamers, and electron microscopy studies of single particles revealed that these hexamers are arranged into ring-like structures with an internal aperture sufficiently large to accommodate the MtrE trimer. Cross-linking of single cysteine mutants of MtrC to stabilize the dimer interface in the presence of MtrE, trapped an MtrC-MtrE complex with a molecular mass consistent with a stoichiometry of 3:6 (MtrE(3)MtrC(6)), suggesting that dimers of MtrC interact with MtrE, presumably by binding to the two grooves. As both MtrE and MtrD are trimeric, our studies suggest that the functional pump is assembled with a stoichiometry of 3:6:3.
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spelling pubmed-31436492011-08-03 Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3 Janganan, Thamarai K. Bavro, Vassiliy N. Zhang, Li Matak-Vinkovic, Dijana Barrera, Nelson P. Venien-Bryan, Catherine Robinson, Carol V. Borges-Walmsley, Maria Inês Walmsley, Adrian R. J Biol Chem Microbiology The multiple transferable resistance (mTR) pump from Neisseria gonorrhoeae MtrCDE multidrug pump is assembled from the inner and outer membrane proteins MtrD and MtrE and the periplasmic membrane fusion protein MtrC. Previously we established that while there is a weak interaction of MtrD and MtrE, MtrC binds with relatively high affinity to both MtrD and MtrE. MtrD conferred antibiotic resistance only when it was expressed with MtrE and MtrC, suggesting that these proteins form a functional tripartite complex in which MtrC bridges MtrD and MtrE. Furthermore, we demonstrated that MtrC interacts with an intraprotomer groove on the surface of MtrE, inducing channel opening. However, a second groove is apparent at the interface of the MtrE subunits, which might also be capable of engaging MtrC. We have now established that MtrC can be cross-linked to cysteines placed in this interprotomer groove and that mutation of residues in the groove impair the ability of the pump to confer antibiotic resistance by locking MtrE in the closed channel conformation. Moreover, MtrE K390C forms an intermolecular disulfide bond with MtrC E149C locking MtrE in the open channel conformation, suggesting that a functional salt bridge forms between these residues during the transition from closed to open channel conformations. MtrC forms dimers that assemble into hexamers, and electron microscopy studies of single particles revealed that these hexamers are arranged into ring-like structures with an internal aperture sufficiently large to accommodate the MtrE trimer. Cross-linking of single cysteine mutants of MtrC to stabilize the dimer interface in the presence of MtrE, trapped an MtrC-MtrE complex with a molecular mass consistent with a stoichiometry of 3:6 (MtrE(3)MtrC(6)), suggesting that dimers of MtrC interact with MtrE, presumably by binding to the two grooves. As both MtrE and MtrD are trimeric, our studies suggest that the functional pump is assembled with a stoichiometry of 3:6:3. American Society for Biochemistry and Molecular Biology 2011-07-29 2011-05-24 /pmc/articles/PMC3143649/ /pubmed/21610073 http://dx.doi.org/10.1074/jbc.M111.246595 Text en © 2011 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles
spellingShingle Microbiology
Janganan, Thamarai K.
Bavro, Vassiliy N.
Zhang, Li
Matak-Vinkovic, Dijana
Barrera, Nelson P.
Venien-Bryan, Catherine
Robinson, Carol V.
Borges-Walmsley, Maria Inês
Walmsley, Adrian R.
Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3
title Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3
title_full Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3
title_fullStr Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3
title_full_unstemmed Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3
title_short Evidence for the Assembly of a Bacterial Tripartite Multidrug Pump with a Stoichiometry of 3:6:3
title_sort evidence for the assembly of a bacterial tripartite multidrug pump with a stoichiometry of 3:6:3
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143649/
https://www.ncbi.nlm.nih.gov/pubmed/21610073
http://dx.doi.org/10.1074/jbc.M111.246595
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