Literature DB >> 28214542

Several hPepT1-transported drugs are substrates of the Escherichia coli proton-coupled oligopeptide transporter YdgR.

Bala K Prabhala1, Nanda G Aduri1, Mazhar Iqbal2, Moazur Rahman2, Michael Gajhede1, Paul R Hansen1, Osman Mirza3.   

Abstract

Proton-dependent oligopeptide transporters (POTs) are secondary active transporters found in all kingdoms of life. POTs utilize the proton electrochemical gradient for the uptake of nutrient dipeptides and tripeptides. The human POT hPepT1 is known to transport a number of drugs. As part of ongoing studies on substrate specificities of POTs from Escherichia coli, our aim in this study was to investigate whether bacterial POTs could also transport these drugs. For this, we selected the common orally administered drugs sulpiride, bestatin, valacyclovir, ampicillin and oseltamivir, that are all transported by hPepT1. The transport of these drugs was evaluated using the prototypical POT YdgR from E. coli. The transport studies were pursued through combining cell-based assays with liquid chromatography-tandem mass spectrometric (LC-MS/MS) analysis. These investigations revealed that YdgR from E. coli is able to transport five (sulpiride, bestatin, valacyclovir, ampicillin and oseltamivir) drugs. Furthermore, cells not overexpressing YdgR were also able to transport these drugs in a POT-like manner. Orthologues of YdgR are found in several species in the gut microbiome; hence, our findings could have implications for further understanding about the interaction between gut microbes and orally administered drugs.
Copyright © 2017 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Bacteria/drug interaction; Bacterial peptide transporters; hPepT1 drugs

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Year:  2017        PMID: 28214542     DOI: 10.1016/j.resmic.2017.01.005

Source DB:  PubMed          Journal:  Res Microbiol        ISSN: 0923-2508            Impact factor:   3.992


  3 in total

1.  The prototypical proton-coupled oligopeptide transporter YdgR from Escherichia coli facilitates chloramphenicol uptake into bacterial cells.

Authors:  Bala K Prabhala; Nanda G Aduri; Neha Sharma; Aqsa Shaheen; Arpan Sharma; Mazhar Iqbal; Paul R Hansen; Christoffer Brasen; Michael Gajhede; Moazur Rahman; Osman Mirza
Journal:  J Biol Chem       Date:  2017-11-17       Impact factor: 5.157

2.  Cryo-EM Structure of an Atypical Proton-Coupled Peptide Transporter: Di- and Tripeptide Permease C.

Authors:  Maxime Killer; Giada Finocchio; Haydyn D T Mertens; Dmitri I Svergun; Els Pardon; Jan Steyaert; Christian Löw
Journal:  Front Mol Biosci       Date:  2022-07-11

3.  Membrane Chemistry Tunes the Structure of a Peptide Transporter.

Authors:  Tanya Lasitza-Male; Kim Bartels; Jakub Jungwirth; Felix Wiggers; Gabriel Rosenblum; Hagen Hofmann; Christian Löw
Journal:  Angew Chem Int Ed Engl       Date:  2020-09-11       Impact factor: 15.336

  3 in total

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