An integrated and continuous downstream process for microbial virus-like particle vaccine biomanufacture

被引:6
作者
Gerstweiler, Lukas [1 ]
Billakanti, Jagan [2 ]
Bi, Jingxiu [1 ]
Middelberg, Anton P. J. [3 ]
机构
[1] Univ Adelaide, Sch Chem Engn & Adv Mat, North Terr, Adelaide, SA 5000, Australia
[2] Global Life Sci Solut Australia Pty Ltd, Parramatta, NSW, Australia
[3] Univ Adelaide, Div Res & Innovat, Adelaide, SA, Australia
关键词
biomanufacture; cont; continuous downstream processing; process integration; vaccine; virus-likeparticle; CELL-CULTURE SUPERNATANT; CONTINUOUS PURIFICATION; PROTEIN; CHROMATOGRAPHY; DESIGN; SIZE; AGGREGATION;
D O I
10.1002/bit.28118
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
In this study, we present the first integrated and continuous downstream process for the production of microbial virus-like particle vaccines. Modular murine polyomavirus major capsid VP1 with integrated J8 antigen was used as a model virus-like particle vaccine. The integrated continuous downstream process starts with crude cell lysate and consists of a flow-through chromatography step followed by periodic counter-current chromatography (PCC) (bind-elute) using salt-tolerant mixed-mode resin and subsequent in-line assembly. The automated process showed a robust behavior over different inlet feed concentrations ranging from 1.0 to 3.2 mg ml(-1) with only minimal adjustments needed, and produced continuously high-quality virus-like particles, free of nucleic acids, with constant purity over extended periods of time. The average size remained constant between 44.8 +/- 2.3 and 47.2 +/- 2.9 nm comparable to literature. The process had an overall product recovery of 88.6% and a process productivity up to 2.56 mg h(-1) ml(resin)(-1) in the PCC step, depending on the inlet concentration. Integrating a flow through step with a subsequent PCC step allowed streamlined processing, showing a possible continuous pathway for a wide range of products of interest.
引用
收藏
页码:2122 / 2133
页数:12
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