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从适应无血清悬浮培养的 CHO 细胞中实验室生产人催乳素。

Laboratory production of human prolactin from CHO cells adapted to serum-free suspension culture.

机构信息

Biotechnology Center, Instituto de Pesquisas Energéticas e Nucleares IPEN-CNEN/SP, Av. Prof. Lineu Prestes 2242, Cidade Universitária, 05508-900 São Paulo, Brazil.

出版信息

Appl Biochem Biotechnol. 2012 Aug;167(8):2212-24. doi: 10.1007/s12010-012-9745-1. Epub 2012 Jun 13.

Abstract

Human prolactin (hPRL) is a polypeptide with 199 amino acids and a molecular mass of 23 kDa. Previously, a eukaryotic hPRL expression vector was used to transfect Chinese hamster ovary (CHO) cells: this work describes a fast and practical laboratory adaptation of these transfected cells, in ~40 days, to grow in suspension in serum-free medium. High cell densities of up to 4.0 × 10(6) cell/ml were obtained from spinner flask cultures and a stable and continuous production process was developed for at least 30 days. Two harvesting strategies were set up, 50 or 100 % of the total conditioned medium being collected daily and replaced by fresh culture medium. The volumetric productivity was 5-7 μg hPRL/ml, as determined directly in the collected medium via reversed-phase HPLC (RP-HPLC). A two-step process based on a cationic exchanger followed by size exclusion chromatography was applied to obtain purified hPRL from conditioned medium. Two hPRL isoforms, non-glycosylated and glycosylated, could also be separated by high-performance size-exclusion chromatography (HPSEC) and, when analyzed by RP-HPLC, HPSEC, Western blotting, and bioassay, were found to be comparable to the World Health Organization International Reference Reagent of hPRL. These results are useful for the practical scale-up to the pilot and industrial scale of a bioprocess based on CHO cell culture.

摘要

人催乳素(hPRL)是一种具有 199 个氨基酸和 23 kDa 分子量的多肽。先前,使用真核 hPRL 表达载体转染中国仓鼠卵巢(CHO)细胞:这项工作描述了这些转染细胞在大约 40 天内在无血清培养基中悬浮生长的快速实用的实验室适应,高细胞密度高达 4.0×10(6)细胞/ml,从摇瓶培养物中获得,并开发了一种稳定且连续的生产工艺,至少持续 30 天。设置了两种收获策略,每天收集和更换新鲜培养基,收集总条件培养基的 50%或 100%。通过反相高效液相色谱(RP-HPLC)直接在收集的培养基中测定的体积产率为 5-7μg hPRL/ml。基于阳离子交换剂的两步工艺随后是分子筛层析,从条件培养基中获得纯化的 hPRL。还可以通过高性能凝胶过滤色谱(HPSEC)分离两种 hPRL 同工型,即非糖基化和糖基化同工型,并且当通过 RP-HPLC、HPSEC、Western blot 和生物测定分析时,发现它们与世界卫生组织 hPRL 国际参考标准品相当。这些结果对于基于 CHO 细胞培养的生物工艺从实验规模扩大到中试和工业规模是有用的。

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