Rapid monitoring of recombinant protein products: a comparison of current technologies

被引:83
作者
Baker, KN [1 ]
Rendall, MH
Patel, A
Boyd, P
Hoare, M
Freedman, RB
James, DC
机构
[1] Univ Kent, Res Sch Biosci, Canterbury CT2 7NJ, Kent, England
[2] GlaxoSmithKline Res & Dev Ltd, Beckenham BR3 3BS, Kent, England
[3] UCL, Adv Ctr Biochem Engn, London WC1E 7JE, England
[4] Univ Queensland, Dept Chem Engn, Brisbane, Qld 4072, Australia
关键词
D O I
10.1016/S0167-7799(01)01914-X
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
Specific measurement of recombinant protein titer in a complex environment during industrial bioprocessing has traditionally relied on labor-intensive and time-consuming immunoassays. In recent years, however, developments in analytical technology have resulted in improved methods for protein product monitoring during bioprocessing. The choice of product-monitoring technology for a particular bioprocess will depend on a variety of assay factors and instrument-specific factors. In this article, we have compiled an overview of the advantages and disadvantages of the most commonly used technologies used: electrochemiluminescence, optical biosensors, rapid chromatography and nephelometry. The advantages of each technology for measuring both small and large recombinant therapeutic proteins are compared with a conventional enzyme-linked immunosorbent assay (ELISA) technique.
引用
收藏
页码:149 / 156
页数:8
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