Strategies for drug target identification in Mycobacterium leprae

被引:7
作者
Acebron-Garcia-de-Eulate, Marta [1 ]
Blundell, Tom L. [1 ]
Vedithi, Sundeep Chaitanya [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Tennis Court Rd, Cambridge CB2 1GA, England
关键词
Hansen's disease; Mycobacterium leprae; Structure-activity relationship; drug target; Structural bioinformatics; DIHYDROPTEROATE SYNTHASE; LEPROSY; TUBERCULOSIS; INHIBITION; GENES; CHALLENGES; MECHANISM; GENOME; POTENT;
D O I
10.1016/j.drudis.2021.03.026
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hansen's disease (HD), or leprosy, continues to be endemic in many parts of the world. Although multidrug therapy (MDT) is successful in curing a large number of patients, some of them abandon it because it is a long-term treatment. Therefore, identification of new drug targets in Mycobacterium leprae is considered of high importance. Here, we introduce an overview of in silico and in vitro studies that might be of help in this endeavor. The essentiality of M. leprae proteins is reviewed with discussion of flux balance analysis, gene expression, and knockout articles. Finally, druggability techniques are proposed for the validation of new M. leprae protein targets (see Fig. 1).
引用
收藏
页码:1569 / 1573
页数:5
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