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基于新型红色荧光蛋白的微孔板分析法,利用石蜡对休眠结核分枝杆菌进行药物筛选。

Novel red fluorescence protein based microplate assay for drug screening against dormant Mycobacterium tuberculosis by using paraffin.

作者信息

Yeware Amar, Sarkar Dhiman

机构信息

Academy of Sciences and Innovative Research (AcSIR), CSIR-NCL Pune, India; Combi Chem Bio Resource Center, Organic Chemistry Division, Dr. Homi Bhabha Road, National Chemical Laboratory, Pune, 411008, Maharashtra, India.

出版信息

Tuberculosis (Edinb). 2018 May;110:15-19. doi: 10.1016/j.tube.2018.02.008. Epub 2018 Feb 26.

Abstract

The hypoxia model of dormancy is widely used in drug screening programs to identify novel inhibitors against latent Mycobacterium tuberculosis disease. In earlier reported microplate assays, hypoxia was maintained by either sealing the microplate or shifting in an anaerobic chamber to develop dormant phenotype. In these assays, inhibitors were added during inoculation, which mainly represents the active stage inhibitors instead of the dormant ones. Herein, the culture was covered with paraffin to develop hypoxia condition and consequently providing the advantage of adding compounds at any stage during incubation of 96-well plate. The stable expression of the red fluorescent protein in the bacilli under both actively growing as well as dormant conditions also facilitate the reliable estimation of growth and inhibition kinetics of bacilli in medium. Furthermore, S/N ratio and Z' factor of this assay were found to be > 27 and 0.91-0.94 respectively, which confirm the robustness of the protocol. This newly developed drug-screening assay offers an easy, inexpensive, safe and high throughput-screening tool to search novel antitubercular inhibitors against both active and dormant bacilli. The red fluorescent H37Ra strain is a suitable surrogate for the more virulent H37Rv strain, and thus this effort will help in combating latent tuberculosis.

摘要

休眠的缺氧模型在药物筛选项目中被广泛用于鉴定针对潜伏性结核分枝杆菌病的新型抑制剂。在早期报道的微孔板试验中,通过密封微孔板或转移至厌氧箱中来维持缺氧状态以形成休眠表型。在这些试验中,抑制剂在接种时添加,这主要代表的是针对活跃期而非休眠期的抑制剂。在此,用石蜡覆盖培养物以形成缺氧条件,从而在96孔板培养期间的任何阶段添加化合物都具有优势。在活跃生长和休眠条件下,红色荧光蛋白在杆菌中的稳定表达也有助于可靠地估计杆菌在培养基中的生长和抑制动力学。此外,该试验的信噪比和Z'因子分别被发现大于27和0.91 - 0.94,这证实了该方案的稳健性。这种新开发的药物筛选试验提供了一种简单、廉价、安全且高通量的筛选工具,用于寻找针对活跃和休眠杆菌的新型抗结核抑制剂。红色荧光H37Ra菌株是更具毒性的H37Rv菌株的合适替代物,因此这项工作将有助于对抗潜伏性结核病。

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