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The Bacterial Type III Secretion System as a Target for Developing New Antibiotics
Author(s) -
McShan Andrew C.,
De Guzman Roberto N.
Publication year - 2015
Publication title -
chemical biology and drug design
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 77
eISSN - 1747-0285
pISSN - 1747-0277
DOI - 10.1111/cbdd.12422
Subject(s) - effector , bacteria , secretion , small molecule , cytoplasm , bacterial cell structure , pathogenic bacteria , biology , antibiotics , biochemistry , chemistry , microbiology and biotechnology , genetics
Antibiotic resistance in pathogens requires new targets for developing novel antibacterials. The bacterial type III secretion system (T3 SS ) is an attractive target for developing antibacterials as it is essential in the pathogenesis of many Gram‐negative bacteria. The T3 SS consists of structural proteins, effectors, and chaperones. Over 20 different structural proteins assemble into a complex nanoinjector that punctures a hole on the eukaryotic cell membrane to allow the delivery of effectors directly into the host cell cytoplasm. Defects in the assembly and function of the T3 SS render bacteria non‐infective. Two major classes of small molecules, salicylidene acylhydrazides and thiazolidinones, have been shown to inhibit multiple genera of bacteria through the T3 SS . Many additional chemically and structurally diverse classes of small molecule inhibitors of the T3 SS have been identified as well. While specific targets within the T3 SS of a few inhibitors have been suggested, the vast majority of specific protein targets within the T3 SS remain to be identified or characterized. Other T3 SS inhibitors include polymers, proteins, and polypeptides mimics. In addition, T3 SS activity is regulated by its interaction with biologically relevant molecules, such as bile salts and sterols, which could serve as scaffolds for drug design.