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用于病毒纯化的不对称流场流分馏方法。

Asymmetric flow field flow fractionation methods for virus purification.

作者信息

Eskelin Katri, Lampi Mirka, Meier Florian, Moldenhauer Evelin, Bamford Dennis H, Oksanen Hanna M

机构信息

Department of Biosciences and Institute of Biotechnology, Viikinkaari 9, University of Helsinki, FIN-00014 Helsinki, Finland.

Postnova Analytics, Max-Planck-Str. 14, 86899 Landsberg, Germany.

出版信息

J Chromatogr A. 2016 Oct 21;1469:108-119. doi: 10.1016/j.chroma.2016.09.055. Epub 2016 Sep 28.

Abstract

Detailed biochemical and biophysical characterization of viruses requires viral preparations of high quantity and purity. The optimization of virus production and purification is an essential, but laborious and time-consuming process. Asymmetric flow field flow fractionation (AF4) is an attractive alternative method for virus purification because it is a rapid and gentle separation method that should preserve viral infectivity. Here we optimized the AF4 conditions to be used for purification of a model virus, bacteriophage PRD1, from various types of starting materials. Our results show that AF4 is well suited for PRD1 purification as monitored by virus recovery and specific infectivity. Short analysis time and high sample loads enabled us to use AF4 for preparative scale purification of PRD1. Furthermore, we show that AF4 enables the rapid real-time analysis of progeny virus production in infected cells.

摘要

对病毒进行详细的生化和生物物理特性分析需要大量且纯净的病毒制剂。病毒生产和纯化的优化是一个必不可少但又费力且耗时的过程。不对称流场流分馏(AF4)是一种颇具吸引力的病毒纯化替代方法,因为它是一种快速且温和的分离方法,有望保留病毒感染力。在此,我们优化了AF4条件,用于从各种起始材料中纯化模型病毒——噬菌体PRD1。我们的结果表明,通过病毒回收率和比感染力监测,AF4非常适合PRD1的纯化。短分析时间和高样品负载量使我们能够将AF4用于PRD1的制备规模纯化。此外,我们表明AF4能够对感染细胞中后代病毒的产生进行快速实时分析。

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