Monitoring of the adenovirus production process by flow cytometry

被引:13
|
作者
Sandhu, Kalbinder Singh [1 ,2 ]
Al-Rubeai, Mohamed [1 ,2 ]
机构
[1] Univ Birmingham, Dept Chem Engn, Birmingham B15 2TT, W Midlands, England
[2] Univ Coll Dublin Belfield, Sch Chem & Bioproc Engn, Dublin 4, Ireland
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1021/bp070198s
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:250 / 261
页数:12
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