金刚乙胺
蛋白质片段互补分析
互补
甲型流感病毒
金刚烷胺
大肠杆菌
化学
突变体
生物
计算生物学
生物物理学
病毒学
病毒
生物化学
基因
作者
Paul Santner,João M. Martins,Jonas S. Laursen,Lars Behrendt,Leise Riber,Christian A. Olsen,Isaiah T. Arkin,Jakob R. Winther,Martin Willemoës,Kresten Lindorff‐Larsen
出处
期刊:Biochemistry
[American Chemical Society]
日期:2018-09-19
卷期号:57 (41): 5949-5956
被引量:17
标识
DOI:10.1021/acs.biochem.8b00721
摘要
The M2 protein is an important target for drugs in the fight against the influenza virus. Because of the emergence of resistance against antivirals directed toward the M2 proton channel, the search for new drugs against resistant M2 variants is of high importance. Robust and sensitive assays for testing potential drug compounds on different M2 variants are valuable tools in this search for new inhibitors. In this work, we describe a fluorescence sensor-based assay, which we termed "pHlux", that measures proton conduction through M2 when synthesized from an expression vector in Escherichia coli. The assay was compared to a previously established bacterial potassium ion transport complementation assay, and the results were compared to simulations obtained from analysis of a computational model of M2 and its interaction with inhibitor molecules. The inhibition of M2 was measured for five different inhibitors, including Rimantadine, Amantadine, and spiro type compounds, and the drug resistance of the M2 mutant variants (swine flu, V27A, and S31N) was confirmed. We demonstrate that the pHlux assay is robust and highly sensitive and shows potential for high-throughput screening.
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