The role of the TolC family in protein transport and multidrug efflux.
- 1 October 2001
- journal article
- review article
- Published by Wiley in European Journal of Biochemistry
- Vol. 268 (19) , 5011-5026
- https://doi.org/10.1046/j.0014-2956.2001.02442.x
Abstract
Gram-negative bacteria are enveloped by a system of two membranes, and they use specialized multicomponent, energy-driven pumps to transport molecules directly across this double-layered partition from the cell interior to the extra-cellular environment. One component of these pumps is embedded in the outer-membrane, and the paradigm for its structure and function is the TolC protein from Escherichia coli. A common component of a wide variety of efflux pumps, TolC and its homologues are involved in the export of chemically diverse molecules ranging from large protein toxins, such as alpha-hemolysin, to small toxic compounds, such as antibiotics. TolC family members thus play important roles in conferring pathogenic bacteria with both virulence and multidrug resistance. These pumps assemble reversibly in a transient process that brings together TolC or its homologue, an inner-membrane-associated periplasmic component, an integral inner-membrane translocase and the substrate itself. TolC can associate in this fashion with a variety of different partners to participate in the transport of diverse substrates. We review here the structure and function of TolC and the other components of the efflux/transport pump.Keywords
This publication has 81 references indexed in Scilit:
- How to untwist an α-helix: structural principles of an α-helical barrel11Edited by J. ThorntonJournal of Molecular Biology, 2001
- Structural stability and domain organization of colicin E1Journal of Molecular Biology, 2000
- ABC-ATPases, adaptable energy generators fuelling transmembrane movement of a variety of molecules in organisms from bacteria to humansJournal of Molecular Biology, 1999
- Alignment and structure prediction of divergent protein families: periplasmic and outer membrane proteins of bacterial efflux pumpsJournal of Molecular Biology, 1999
- Shear numbers of protein β-barrels: definition refinements and statisticsJournal of Molecular Biology, 1998
- Channel specificity: structural basis for sugar discrimination and differential flux rates in maltoporin 1 1Edited by R. HuberJournal of Molecular Biology, 1997
- Refined Structure of the Porin from Rhodopseudomonas blasticaJournal of Molecular Biology, 1994
- TolC of Escherichia coli Functions as an Outer Membrane ChannelZentralblatt für Bakteriologie, 1993
- Structure of porin refined at 1.8 Å resolutionJournal of Molecular Biology, 1992
- X-Ray Structure of the GCN4 Leucine Zipper, a Two-Stranded, Parallel Coiled CoilScience, 1991