Department of Chemistry, Pennsylvania State University , University Park, Pennsylvania 16802, United States.
Novartis Institutes for BioMedical Research, Inc., 5300 Chiron Way, Emeryville, California 94608-2916, United States.
Anal Chem. 2017 May 2;89(9):5050-5057. doi: 10.1021/acs.analchem.7b00466. Epub 2017 Apr 15.
The inherent difficulty of discovering new and effective antibacterials and the rapid development of resistance particularly in Gram-negative bacteria, illustrates the urgent need for new methods that enable rational drug design. Here we report the development of 3D imaging cluster Time-of-Flight secondary ion mass spectrometry (ToF-SIMS) as a label-free approach to chemically map small molecules in aggregated and single Escherichia coli cells, with ∼300 nm spatial resolution and high chemical sensitivity. The feasibility of quantitative analysis was explored, and a nonlinear relationship between treatment dose and signal for tetracycline and ampicillin, two clinically used antibacterials, was observed. The methodology was further validated by the observation of reduction in tetracycline accumulation in an E. coli strain expressing the tetracycline-specific efflux pump (TetA) compared to the isogenic control. This study serves as a proof-of-concept for a new strategy for chemical imaging at the nanoscale and has the potential to aid discovery of new antibacterials.
发现新的有效抗菌药物存在固有难度,尤其是革兰氏阴性菌的耐药性迅速发展,这说明了我们迫切需要新的方法,以实现合理的药物设计。在这里,我们报告了三维成像簇飞行时间二次离子质谱(ToF-SIMS)的发展,它是一种无需标记即可对聚集态和单个大肠杆菌细胞中的小分子进行化学绘图的方法,具有约 300nm 的空间分辨率和高化学灵敏度。我们还探索了定量分析的可行性,并观察到两种临床使用的抗菌药物四环素和氨苄西林的处理剂量与信号之间呈非线性关系。通过观察表达四环素特异性外排泵(TetA)的大肠杆菌菌株与同源对照相比四环素积累减少,进一步验证了该方法的有效性。这项研究为纳米尺度化学成像的新策略提供了概念验证,并有可能有助于发现新的抗菌药物。