Literature DB >> 21657235

Role of water during the extrusion of substrates by the efflux transporter AcrB.

Robert Schulz1, Attilio V Vargiu, Paolo Ruggerone, Ulrich Kleinekathöfer.   

Abstract

The major efflux system in Escherichia coli is the tripartite complex AcrAB-TolC. Its homotrimeric transporter AcrB is polyspecific and extrudes antibiotics out of the bacterium. This extrusion is performed via a functional rotation, in which each monomer assumes a particular conformation. In the present study, targeted molecular dynamics simulations have been employed to obtain a molecular level understanding of the transport process. A particular focus is put on the role of water molecules in this extrusion process. It is shown that the water flows from the binding pocket toward the exit gate in the extrusion step and helps the substrate to move along this path. These results are underpinned by a detailed analysis of the electrostatic interaction energy. Furthermore, the role of water for the polyspecificity of the transporter is discussed.

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Year:  2011        PMID: 21657235     DOI: 10.1021/jp200996x

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  12 in total

1.  Coarse-grained simulations of conformational changes in the multidrug efflux transporter AcrB.

Authors:  Yead Jewel; Jin Liu; Prashanta Dutta
Journal:  Mol Biosyst       Date:  2017-09-26

Review 2.  The challenge of efflux-mediated antibiotic resistance in Gram-negative bacteria.

Authors:  Xian-Zhi Li; Patrick Plésiat; Hiroshi Nikaido
Journal:  Clin Microbiol Rev       Date:  2015-04       Impact factor: 26.132

3.  Molecular mechanism of MBX2319 inhibition of Escherichia coli AcrB multidrug efflux pump and comparison with other inhibitors.

Authors:  Attilio V Vargiu; Paolo Ruggerone; Timothy J Opperman; Son T Nguyen; Hiroshi Nikaido
Journal:  Antimicrob Agents Chemother       Date:  2014-08-11       Impact factor: 5.191

4.  Substrate-dependent transport mechanism in AcrB of multidrug resistant bacteria.

Authors:  Yead Jewel; Quyen Van Dinh; Jin Liu; Prashanta Dutta
Journal:  Proteins       Date:  2020-02-08

Review 5.  Recent advances toward a molecular mechanism of efflux pump inhibition.

Authors:  Timothy J Opperman; Son T Nguyen
Journal:  Front Microbiol       Date:  2015-05-05       Impact factor: 5.640

6.  Computational study of correlated domain motions in the AcrB efflux transporter.

Authors:  Robert Schulz; Attilio V Vargiu; Paolo Ruggerone; Ulrich Kleinekathöfer
Journal:  Biomed Res Int       Date:  2015-01-05       Impact factor: 3.411

Review 7.  Molecular Dynamics Computer Simulations of Multidrug RND Efflux Pumps.

Authors:  Paolo Ruggerone; Attilio V Vargiu; Francesca Collu; Nadine Fischer; Christian Kandt
Journal:  Comput Struct Biotechnol J       Date:  2013-03-03       Impact factor: 7.271

8.  Substrate binding accelerates the conformational transitions and substrate dissociation in multidrug efflux transporter AcrB.

Authors:  Beibei Wang; Jingwei Weng; Wenning Wang
Journal:  Front Microbiol       Date:  2015-04-13       Impact factor: 5.640

9.  Stepwise substrate translocation mechanism revealed by free energy calculations of doxorubicin in the multidrug transporter AcrB.

Authors:  Zhicheng Zuo; Beibei Wang; Jingwei Weng; Wenning Wang
Journal:  Sci Rep       Date:  2015-09-14       Impact factor: 4.379

Review 10.  Interaction of antibacterial compounds with RND efflux pumps in Pseudomonas aeruginosa.

Authors:  Jürg Dreier; Paolo Ruggerone
Journal:  Front Microbiol       Date:  2015-07-08       Impact factor: 5.640

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