A key bacterial cytoskeletal cell division protein FtsZ as a novel therapeutic antibacterial drug target

被引:24
作者
Rahman, Mujeeb Ur [1 ]
Wang, Ping [2 ]
Wang, Na [1 ]
Chen, Yaodong [1 ]
机构
[1] Northwest Univ, Coll Life Sci, Minist Educ, Key Lab Resources Biol & Biotechnol Western China, 229 Taibai North Rd, Xian 710069, Shaanxi, Peoples R China
[2] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
基金
中国国家自然科学基金;
关键词
FtsZ; multidrug resistance; cell division; antimicrobial; inhibitors; natural antimicrobial compounds; SMALL-MOLECULE INHIBITORS; ESCHERICHIA-COLI; ASSEMBLY DYNAMICS; BACILLUS-SUBTILIS; GTPASE ACTIVITY; IN-VITRO; PEPTIDOGLYCAN SYNTHESIS; VANILLIN DERIVATIVES; CRYSTAL-STRUCTURE; NATURAL-PRODUCTS;
D O I
10.17305/bjbms.2020.4597
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Nowadays, the emergence of multidrug-resistant bacterial strains initiates the urgent need for the elucidation of the new drug targets for the discovery of antimicrobial drugs. Filamenting temperature-sensitive mutant Z (FtsZ), a eukaryotic tubulin homolog, is a GTP-dependent prokaryotic cytoskeletal protein and is conserved among most bacterial strains. In vitro studies revealed that FtsZ self-assembles into dynamic proto filaments or bundles and forms a dynamic Z-ring at the center ofthe cell in vivo, leading to septation and consequent cell division. Speculations on the ability of FtsZ in the blockage of cell division make FtsZ a highly attractive target for developing novel antibiotics. Researchers have been working on synthetic molecules and natural products as inhibitors of FtsZ. Accumulating data suggest that FtsZ may provide the platform for the development of novel antibiotics. In this review, we summarize recent advances in the properties of FtsZ protein and bacterial cell division, as well as in the development of FtsZ inhibitors.
引用
收藏
页码:310 / 318
页数:9
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