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Common recognition topology of mex transporters of Pseudomonas aeruginosa revealed by molecular modelling

Affiliation
Department of Physics ,University of Cagliari ,Monserrato (CA) ,Italy
Catte, Andrea;
Affiliation
Department of Physics ,University of Cagliari ,Monserrato (CA) ,Italy
K. Ramaswamy, Venkata;
Affiliation
Department of Physics ,University of Cagliari ,Monserrato (CA) ,Italy
Vargiu, Attilio Vittorio;
Affiliation
Department of Physics ,University of Cagliari ,Monserrato (CA) ,Italy
Malloci, Giuliano;
Affiliation
Department of Physics ,University of Cagliari ,Monserrato (CA) ,Italy
Bosin, Andrea;
Affiliation
Department of Physics ,University of Cagliari ,Monserrato (CA) ,Italy
Ruggerone, Paolo

The secondary transporters of the resistance-nodulation-cell division (RND) superfamily mediate multidrug resistance in Gram-negative bacteria like Pseudomonas aeruginosa . Among these RND transporters, MexB, MexF, and MexY, with partly overlapping specificities, have been implicated in pathogenicity. Only the structure of the former has been resolved experimentally, which together with the lack of data about the functional dynamics of the full set of transporters, limited a systematic investigation of the molecular determinants defining their peculiar and shared features. In a previous work (Ramaswamy et al., Front. Microbiol., 2018, 9, 1144), we compared at an atomistic level the two main putative recognition sites (named access and deep binding pockets) of MexB and MexY. In this work, we expand the comparison by performing extended molecular dynamics (MD) simulations of these transporters and the pathologically relevant transporter MexF. We employed a more realistic model of the inner phospholipid membrane of P. aeruginosa and more accurate force-fields. To elucidate structure/dynamics-activity relationships we performed physico-chemical analyses and mapped the binding propensities of several organic probes on all transporters. Our data revealed the presence, also in MexF, of a few multifunctional sites at locations equivalent to the access and deep binding pockets detected in MexB. Furthermore, we report for the first time about the multidrug binding abilities of two out of five gates of the channels deputed to peripheral (early) recognition of substrates. Overall, our findings help to define a common “recognition topology” characterizing Mex transporters, which can be exploited to optimize transport and inhibition propensities of antimicrobial compounds.

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License Holder: Copyright © 2022 Catte, K. Ramaswamy, Vargiu, Malloci, Bosin and Ruggerone.

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