Assembly and transport mechanism of tripartite drug efflux systems

Biochim Biophys Acta. 2009 May;1794(5):817-25. doi: 10.1016/j.bbapap.2009.02.017. Epub 2009 Mar 13.

Abstract

Multidrug efflux (MDR) pumps remove a variety of compounds from the cell into the external environment. There are five different classes of MDR pumps in bacteria, and quite often a single bacterial species expresses multiple classes of pumps. Although under normal circumstances MDR pumps confer low-level intrinsic resistance to drugs, the presence of drugs and mutations in regulatory genes lead to high level expression of MDR pumps that can pose problems with therapeutic treatments. This review focuses on the resistance nodulation cell division (RND)-class of MDR pumps that assemble from three proteins. Significant recent advancement in structural aspects of the three pump components has shed new light on the mechanism by which the tripartite efflux pumps extrude drugs. This new information will be critical in developing inhibitors against MDR pumps to improve the potency of prescribed drugs.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Antigens, Bacterial / chemistry
  • Bacterial Outer Membrane Proteins / metabolism
  • Bacterial Proteins / chemistry
  • Biological Transport
  • Drug Resistance, Multiple, Bacterial / physiology*
  • Escherichia coli Proteins / metabolism
  • Lipoproteins / metabolism
  • Membrane Fusion Proteins / chemistry
  • Membrane Fusion Proteins / metabolism
  • Membrane Transport Proteins / metabolism*
  • Multidrug Resistance-Associated Proteins / metabolism
  • Pharmaceutical Preparations / metabolism
  • Protein Structure, Tertiary

Substances

  • AcrA protein, E coli
  • AcrB protein, E coli
  • Antigens, Bacterial
  • Bacterial Outer Membrane Proteins
  • Bacterial Proteins
  • Escherichia coli Proteins
  • Lipoproteins
  • Membrane Fusion Proteins
  • Membrane Transport Proteins
  • Multidrug Resistance-Associated Proteins
  • Pharmaceutical Preparations
  • YajC protein, Brucella
  • tolC protein, E coli