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针对人类免疫缺陷病毒HIV-1的人源单克隆抗体的中试规模生产。

Pilot scale production of a human monoclonal antibody against human immunodeficiency virus HIV-1.

作者信息

Jungbauer A, Tauer C, Wenisch E, Steindl F, Purtscher M, Reiter M, Unterluggauer F, Buchacher A, Uhl K, Katinger H

机构信息

Institute of Applied Microbiology, University of Agriculture and Forestry, Vienna, Austria.

出版信息

J Biochem Biophys Methods. 1989 Aug-Sep;19(2-3):223-40. doi: 10.1016/0165-022x(89)90029-8.

Abstract

Human monoclonal antibodies against the transmembrane protein gp41 of HIV-1 were isolated and purified on a pilot scale. A purification scheme was established for the production of human monoclonal antibodies on the gram scale. 50 1 of culture supernatant can be treated in one purification cycle. The hybridomas were mass cultured in an airlift fermenter. The culture broth was clarified by microfiltration and chromatographed on CM-Sepharose fast flow and protein A Superose. Scale up of the high performance affinity chromatography from 1 ml protein A Superose up to 40 ml is described. All desalting steps were performed by gel filtration on Sephadex G-25 coarse. The yield of the whole purification procedure is in the range of 50-60%. The purity is higher than 99.9%. DNA and reverse transcriptase could not be detected. The whole method is designed as a basis for scale up to industrial scale. Results from quality control assays have proven the validity of this approach.

摘要

已小规模分离并纯化了针对HIV-1跨膜蛋白gp41的人单克隆抗体。建立了一种用于克级规模生产人单克隆抗体的纯化方案。一个纯化循环可处理50升培养上清液。杂交瘤细胞在气升式发酵罐中进行大规模培养。培养液通过微滤澄清,然后在CM-琼脂糖快速流动柱和蛋白A超级琼脂糖柱上进行色谱分离。描述了从1毫升蛋白A超级琼脂糖柱放大到40毫升的高效亲和色谱法。所有脱盐步骤均通过在Sephadex G-25粗粒上进行凝胶过滤来完成。整个纯化过程的产率在50%-60%范围内。纯度高于99.9%。未检测到DNA和逆转录酶。整个方法被设计为扩大到工业规模的基础。质量控制分析结果证明了该方法的有效性。

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