Genomics-based identification of targets in pathogenic bacteria for potential therapeutic and diagnostic use

被引:42
|
作者
Raczniak, G
Ibba, M
Söll, D
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[2] Panum Inst, Lab B, Dept Med Biochem & Genet, Ctr Biomol Recognit, DK-2200 Copenhagen, Denmark
[3] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[4] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
关键词
aminoacyl-tRNA; amidotransferase; genomics; evolution; protein synthesis; tRNA; Chlamydia; sexually transmitted disease; Borrelia; Lyme disease;
D O I
10.1016/S0300-483X(00)00454-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The availability of numerous complete microbial genome sequences has profoundly altered our understanding of a number of fundamental biological processes. For example the enzymes involved in aminoacyl-tRNA (AA-tRNA) synthesis, the key process responsible for the accuracy of protein synthesis, have been found to be highly species-specific. In particular, a number of pathogens contain certain pathways of AA-tRNA synthesis that are unrelated to those found in their mammalian hosts. Since AA-tRNA synthesis is indispensable for cell viability, the discovery of pathogen-specific pathways and enzymes presents novel therapeutic and diagnostic targets. Here we will review recent advances in the elucidation of AA-tRNA synthesis pathways and discuss the possible pharmaceutical exploitation of these discoveries. In particular, the integration of genomic and biochemical approaches to identify novel targets for the treatment of Chlamydial infections and the diagnosis and treatment of Lyme disease will be presented. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:181 / 189
页数:9
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