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检测分枝杆菌生长抑制剂的快速方法。

Rapid methods for testing inhibitors of mycobacterial growth.

作者信息

Evangelopoulos Dimitrios, Bhakta Sanjib

机构信息

Faculty of Science/ Institute of Structural and Molecular Biology, Birkbeck College, School of Biological and Chemical Sciences, University of London, London, UK.

出版信息

Methods Mol Biol. 2010;642:193-201. doi: 10.1007/978-1-60327-279-7_15.

Abstract

Considering the increased concerns with controlling infectious epidemics such as tuberculosis, a global concerted effort (WHO) is now dead-lined to tackle the emergence of extensive drug resistance through identifying a novel line of therapeutics which will on the one hand shorten the course of treatment and on the other is also expected to be effective against the emerging resistant strains. Major problems with the preclinical drug screening against the uniquely slow-growing pathogen Mycobacterium tuberculosis are either found expensive, time-consuming, or require a highly complex laboratory setup. A rapid and convenient, although relatively inexpensive, method requiring very little consumption of inhibitors within a simple microbiology setup for antimycobacterial screening is thus timely. The spot-culture growth inhibition assay aims to test the biological activity of a number of newly discovered natural products and thousands of novel chemicals synthesized on the basis of basic structural and molecular biology studies. Many different classes of novel chemical entities are now independently prepared around the world by distinguished chemists on the chemical behavior of the group of molecules. To serve the purpose of antimycobacterials screening, we aim to describe a method in this chapter performed in a six-well plate format. This method can also be extended accurately to a 96-well plate format according to the necessity of the project. In addition to evaluating a range of prospective drug candidates, this method would also contribute to elucidate substrates for many putative endogenous pathways through comparing the chemical inhibition with the corresponding genetic modification.

摘要

鉴于对控制诸如结核病等传染性流行病的关注度不断提高,目前全球正在齐心协力(世界卫生组织),通过确定一种新的治疗方法来应对广泛耐药性的出现,这种方法一方面将缩短治疗疗程,另一方面预计对新出现的耐药菌株也有效。针对生长极其缓慢的病原体结核分枝杆菌进行临床前药物筛选存在的主要问题是,要么成本高昂、耗时,要么需要高度复杂的实验室设置。因此,一种快速便捷、相对便宜且在简单微生物学设置中对抗结核分枝杆菌进行筛选时抑制剂消耗极少的方法应运而生。斑点培养生长抑制试验旨在测试许多新发现的天然产物以及基于基础结构和分子生物学研究合成的数千种新型化学品的生物活性。世界各地的杰出化学家现在根据分子组的化学行为独立制备了许多不同类别的新型化学实体。为了实现抗结核分枝杆菌筛选的目的,我们旨在本章中描述一种在六孔板形式下进行的方法。根据项目需要,该方法也可准确扩展到96孔板形式。除了评估一系列潜在的候选药物外,该方法还将通过比较化学抑制与相应的基因修饰,有助于阐明许多假定的内源性途径的底物。

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