r-PAI-2治疗蛋白的酵母菌特异性HCP测定

G. Rajasekariah
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引用次数: 0

摘要

每当宿主细胞用于重组体的繁殖时,一定会遇到一些杂质,它们总是宿主细胞成分,是最终重组蛋白的一部分。这是首次在重组宿主“酵母细胞”酿酒酵母的情况下进行研究。在非常小心的情况下,使用基因缺失(空细胞)酵母组分产生针对酵母蛋白的高亲和力抗体,该组分通过下游技术用适当的树脂纯化用于柱纯化,并且这些抗体被用于构建特异性夹心ELISA系统,以监测宿主污染物蛋白(HCP)的程度。这是如何做到的,遵循了什么战略方法,HCP检测ELISA系统是如何构建的,限制是什么?。对这些要点进行了描述和讨论,并对HCP在强化治疗蛋白制备中的前景进行了展望。我们的HCP测定足够灵敏,可以检测最终PAI-2产物中的200-250ppm。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Saccharomyces Specific- HCP Assay for r-PAI-2 Therapeutic Proteins
Whenever a host cell is employed for a means of propagation of recombinants, some impurities are bound to come across and they are invariably of host cell components and are part of final recombinant proteins. These are investigated for the first time in case of recombinant host, “yeast cells” Saccharomyces. With great care, high affinity antibodies are generated for yeast proteins using Gene-minus (null-cell) yeast components purified by down-stream techniques with appropriate resins for column purification and these antibodies are being used to construct specific sandwich ELISA system to monitor the degree of host contaminants proteins (HCPs). How this is being done and what strategic methods are followed and how the HCP- detection ELISA systems are constructed and what are the limitations?. These points are described and discussed along with prospects of HCPs in the intensified therapeutic proteins preparation. Our HCP assay is sensitive enough to detect 200-250 ppm in the final PAI-2 product.
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