| Literature DB >> 2584609 |
A Jungbauer1, C Tauer, E Wenisch, F Steindl, M Purtscher, M Reiter, F Unterluggauer, A Buchacher, K Uhl, H Katinger.
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.Entities:
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Year: 1989 PMID: 2584609 DOI: 10.1016/0165-022x(89)90029-8
Source DB: PubMed Journal: J Biochem Biophys Methods ISSN: 0165-022X