针对流感的高通量细胞免疫荧光测定。

IF 2.7 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Yohanka Martinez-Gzegozewska, Lynn Rasmussen, Sara McKellip, Anna Manuvakhova, N. Miranda Nebane, Andrew J. Reece, Pedro Ruiz, Melinda Sosa, Robert Bostwick, Paige Vinson
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引用次数: 0

摘要

对有可能达到大流行状态的流感疫情做出快速药物发现反应,可以减少识别抗流感药物的时间,从而有助于将病毒的影响降至最低。尽管在寻找新药的过程中考虑了几种抗流感策略,但只有少数治疗剂被批准用于临床。流感病毒在Madin-Darby犬肾(MDCK)细胞中诱导的细胞病变作用已被广泛用于高通量抗流感药物筛选,但MDCK细胞不是人细胞的事实在寻找新的人类使用的治疗剂时构成了缺点。我们已经开发了一种高灵敏度的基于细胞的成像测定法,用于鉴定使用A549人类细胞系的高通量兼容的甲型流感和乙型流感病毒抑制剂。该测定法还被优化用于在不存在胰蛋白酶的情况下评估抗流感抗体的中和作用,这允许测试纯化的抗体和血清样品。该测定平台可应用于全高通量筛选活动或需要定量效价测定结构-活性关系的后期阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-Throughput cell-based immunofluorescence assays against influenza

A rapid drug discovery response to influenza outbreaks with the potential to reach pandemic status could help minimize the virus's impact by reducing the time to identify anti-influenza drugs. Although several anti-influenza strategies have been considered in the search for new drugs, only a few therapeutic agents are approved for clinical use. The cytopathic effect induced by the influenza virus in Madin Darby canine kidney (MDCK) cells has been widely used for high-throughput anti-influenza drug screening, but the fact that the MDCK cells are not human cells constitutes a disadvantage when searching for new therapeutic agents for human use. We have developed a highly sensitive cell-based imaging assay for the identification of inhibitors of influenza A and B virus that is high-throughput compatible using the A549 human cell line. The assay has also been optimized for the assessment of the neutralizing effect of anti-influenza antibodies in the absence of trypsin, which allows testing of purified antibodies and serum samples. This assay platform can be applied to full high-throughput screening campaigns or later stages requiring quantitative potency determinations for structure-activity relationships.

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来源期刊
SLAS Discovery
SLAS Discovery Chemistry-Analytical Chemistry
CiteScore
7.00
自引率
3.20%
发文量
58
审稿时长
39 days
期刊介绍: Advancing Life Sciences R&D: SLAS Discovery reports how scientists develop and utilize novel technologies and/or approaches to provide and characterize chemical and biological tools to understand and treat human disease. SLAS Discovery is a peer-reviewed journal that publishes scientific reports that enable and improve target validation, evaluate current drug discovery technologies, provide novel research tools, and incorporate research approaches that enhance depth of knowledge and drug discovery success. SLAS Discovery emphasizes scientific and technical advances in target identification/validation (including chemical probes, RNA silencing, gene editing technologies); biomarker discovery; assay development; virtual, medium- or high-throughput screening (biochemical and biological, biophysical, phenotypic, toxicological, ADME); lead generation/optimization; chemical biology; and informatics (data analysis, image analysis, statistics, bio- and chemo-informatics). Review articles on target biology, new paradigms in drug discovery and advances in drug discovery technologies. SLAS Discovery is of particular interest to those involved in analytical chemistry, applied microbiology, automation, biochemistry, bioengineering, biomedical optics, biotechnology, bioinformatics, cell biology, DNA science and technology, genetics, information technology, medicinal chemistry, molecular biology, natural products chemistry, organic chemistry, pharmacology, spectroscopy, and toxicology. SLAS Discovery is a member of the Committee on Publication Ethics (COPE) and was published previously (1996-2016) as the Journal of Biomolecular Screening (JBS).
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