Acebrón-García-de-Eulate Marta, Blundell Tom L, Vedithi Sundeep Chaitanya
Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1GA, UK.
Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1GA, UK.
Drug Discov Today. 2021 Jul;26(7):1569-1573. doi: 10.1016/j.drudis.2021.03.026. Epub 2021 Mar 31.
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).
麻风病(HD),即麻风,在世界许多地区仍然流行。尽管多药联合疗法(MDT)成功治愈了大量患者,但其中一些患者因治疗周期长而放弃治疗。因此,确定麻风分枝杆菌新的药物靶点被认为至关重要。在此,我们介绍一些可能有助于这一研究的计算机模拟和体外研究综述。本文回顾了麻风分枝杆菌蛋白质的必要性,并讨论了通量平衡分析、基因表达和基因敲除相关文章。最后,提出了药物可开发性技术以验证新的麻风分枝杆菌蛋白质靶点(见图1)。