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通过流式细胞术监测腺病毒生产过程。

Monitoring of the adenovirus production process by flow cytometry.

作者信息

Sandhu Kalbinder Singh, Al-Rubeai Mohamed

机构信息

Department of Chemical Engineering, University of Birmingham, Edgbaston Birmingham, B15 2TT, United Kingdom.

出版信息

Biotechnol Prog. 2008 Jan-Feb;24(1):250-61. doi: 10.1021/bp070198s. Epub 2007 Dec 11.

Abstract

Adenovirus (Ad) has become the vector of choice for gene therapy clinical protocols worldwide; it is the only viral vector to date that has been licensed for use in a gene therapy treatment. There is, however, a need to develop a simple, reliable at-line method to monitor the production of virus and recombinant proteins (r-proteins) that have no intrinsic reporter properties. Here we utilize flow cytometry to measure cell size, granularity, and DNA content in a single-step analysis and to correlate these parameters to the production of a type-5 Ad (Ad5) expressing the recombinant green fluorescent protein (GFP). Clear correlations between these parameters and productivity are made, with forward scatter and DNA content showing the highest correlation coefficients, 0.9 and 0.83 for virus production and r-protein production, respectively. Measuring these parameters requires little or no processing of the cells from culture to analysis. These parameters have been used successfully to monitor, at-line, the amount of Ad and r-protein product in a 293-Ad system.

摘要

腺病毒(Ad)已成为全球基因治疗临床方案的首选载体;它是迄今为止唯一已获许可用于基因治疗的病毒载体。然而,需要开发一种简单、可靠的在线方法来监测不具有内在报告特性的病毒和重组蛋白(r蛋白)的产生。在这里,我们利用流式细胞术在单步分析中测量细胞大小、粒度和DNA含量,并将这些参数与表达重组绿色荧光蛋白(GFP)的5型腺病毒(Ad5)的产生相关联。这些参数与生产率之间建立了明确的相关性,前向散射和DNA含量显示出最高的相关系数,病毒产生和r蛋白产生的相关系数分别为0.9和0.83。测量这些参数几乎不需要对细胞进行从培养到分析的处理。这些参数已成功用于在线监测293-Ad系统中Ad和r蛋白产物的量。

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