Abstract
Type III Secretion Systems (T3SSs) are highly organized multi-protein nanomachines which translocate effector proteins from the bacterial cytosol directly into host cells. These systems are required for the pathogenesis of a wide array of Gram-negative bacterial pathogens, and thus have attracted attention as potential antibacterial drug targets. A decade of research has enabled the identification of natural products, conventional small molecule drug-like structures, and proteins that inhibit T3SSs. The mechanism(s) of action and molecular target(s) of the majority of these inhibitors remain to be determined. At the same time, structural biology methods are providing an increasingly detailed picture of the functional arrangement of the T3SS component proteins. The confluence of these two research areas may ultimately identify non-classical drug targets and facilitate the development of novel therapeutics.
Keywords: Type III secretion, virulence, Gram-negative bacteria, high-throughput screening, antibiotic drug discovery, T3SSs, Caminosides, Guadinomines, structural biology, benzanilides
Current Drug Targets
Title: The Type III Secretion System as a Source of Novel Antibacterial Drug Targets
Volume: 13 Issue: 3
Author(s): Toni Kline, Heather B. Felise, Sarah Sanowar and Samuel I. Miller
Affiliation:
Keywords: Type III secretion, virulence, Gram-negative bacteria, high-throughput screening, antibiotic drug discovery, T3SSs, Caminosides, Guadinomines, structural biology, benzanilides
Abstract: Type III Secretion Systems (T3SSs) are highly organized multi-protein nanomachines which translocate effector proteins from the bacterial cytosol directly into host cells. These systems are required for the pathogenesis of a wide array of Gram-negative bacterial pathogens, and thus have attracted attention as potential antibacterial drug targets. A decade of research has enabled the identification of natural products, conventional small molecule drug-like structures, and proteins that inhibit T3SSs. The mechanism(s) of action and molecular target(s) of the majority of these inhibitors remain to be determined. At the same time, structural biology methods are providing an increasingly detailed picture of the functional arrangement of the T3SS component proteins. The confluence of these two research areas may ultimately identify non-classical drug targets and facilitate the development of novel therapeutics.
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Cite this article as:
Kline Toni, B. Felise Heather, Sanowar Sarah and I. Miller Samuel, The Type III Secretion System as a Source of Novel Antibacterial Drug Targets, Current Drug Targets 2012; 13 (3) . https://dx.doi.org/10.2174/138945012799424642
DOI https://dx.doi.org/10.2174/138945012799424642 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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