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评估毕赤酵母大规模表达重组乙型肝炎表面抗原过程中病毒样颗粒的形成和 r-HBsAg 的聚集。

Assessing virus like particles formation and r-HBsAg aggregation during large scale production of recombinant hepatitis B surface antigen from Pichia pastoris.

机构信息

Department of recombinant Hepatitis B Vaccine, Production and Research Complex, Pasteur Institute of Iran, Iran.

Biotechnology Group, Faculty of Chemical Engineering, Tarbiat Modares University, Tehran, Iran.

出版信息

Int J Biol Macromol. 2019 Oct 15;139:697-711. doi: 10.1016/j.ijbiomac.2019.08.019. Epub 2019 Aug 2.

DOI:10.1016/j.ijbiomac.2019.08.019
PMID:31381908
Abstract

The aggregation of recombinant proteins in the different stages of purification leads to the loss of a considerable portion of target protein and reduction in the process efficiency. As the active HBsAg used in Hepatitis B vaccine production is in the form of virus-like particle (VLP), therefore the time and stages at which the VLP assembling happened through the process would be important. The aim of this study was to explore the product aggregation during different stages of large scale production of rHBsAg in Pichia pastoris at production unit of the Pasteur Institute of Iran. Dynamic light scattering (DLS) and transmission electron microscopy (TEM), and also size exclusion-high-performance liquid chromatography (SE-HPLC) were carried out on samples taken from each downstream processes steps to determine the rate of VLPs formation as the desired product and the aggregated form at each stage of the purification. Based on the results, it was found that VLPs formation started at the acid precipitation stage and reached up to 80% at the thermal treatment stage. The ultrafiltration, ion exchange chromatography and immunoaffinity chromatography stages were disclosed to have the highest contribution in the formation of VLP (virus like particle) 22 nm.

摘要

在不同的纯化阶段,重组蛋白的聚集会导致目标蛋白的大量损失,并降低过程效率。由于乙型肝炎疫苗生产中使用的活性 HBsAg 是以病毒样颗粒 (VLP) 的形式存在的,因此 VLP 通过该过程组装发生的时间和阶段将非常重要。本研究旨在探索伊朗巴斯德研究所生产单位在毕赤酵母中大规模生产 rHBsAg 的不同阶段的产物聚集情况。对每个下游工艺步骤中取出的样品进行动态光散射 (DLS) 和透射电子显微镜 (TEM) 以及分子筛高效液相色谱 (SE-HPLC) 分析,以确定作为期望产物的 VLPs 形成率,以及在每个纯化阶段的聚集形式。结果表明,VLP 的形成始于酸沉淀阶段,在热处理阶段达到 80%。超滤、离子交换色谱和免疫亲和色谱阶段被揭示在 22nm 病毒样颗粒 (VLP) 的形成中具有最高的贡献。

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