Department of Chemistry, University of California, Berkeley, CA, 94720, USA.
Department of Chemistry, Stanford University, Stanford, CA, 94305, USA.
Angew Chem Int Ed Engl. 2018 May 4;57(19):5267-5272. doi: 10.1002/anie.201712020. Epub 2018 Apr 14.
Front-line tuberculosis (TB) drugs have been characterized extensively in vitro and in vivo with respect to gene expression and cell viability. However, little work has been devoted to understanding their effects on the physiology of the cell envelope, one of the main targets of this clinical regimen. Herein, we use metabolic labeling methods to visualize the effects of TB drugs on cell envelope dynamics in mycobacterial species. We developed a new fluorophore-trehalose conjugate to visualize trehalose monomycolates of the mycomembrane using super-resolution microscopy. We also probed the relationship between mycomembrane and peptidoglycan dynamics using a dual metabolic labeling strategy. Finally, we found that metabolic labeling of both cell envelope structures reports on drug effects on cell physiology in two hours, far faster than a genetic sensor of cell envelope stress. Our work provides insight into acute drug effects on cell envelope biogenesis in live mycobacteria.
一线抗结核药物(TB 药物)在基因表达和细胞活力方面已经在体外和体内得到了广泛的研究。然而,很少有工作致力于了解它们对细胞包膜生理学的影响,细胞包膜是这一临床方案的主要靶点之一。在此,我们使用代谢标记方法来可视化 TB 药物对分枝杆菌物种细胞包膜动力学的影响。我们开发了一种新的荧光素-海藻糖缀合物,用于使用超分辨率显微镜可视化细胞膜海藻糖单脂的动态。我们还使用双重代谢标记策略研究了细胞膜和肽聚糖动力学之间的关系。最后,我们发现,两种细胞包膜结构的代谢标记都可以在两小时内报告药物对细胞生理学的影响,这比细胞膜应激的遗传传感器快得多。我们的工作为急性药物对活分枝杆菌中细胞包膜生物发生的影响提供了新的见解。