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Deciphering the Mechanisms of Therapeutic Protein Production

机译:阐明治疗性蛋白质生产的机制

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Preduction of therapeutic recombinant proteins from mammalian systems is one of the fastest growing segments of the pharmaceutical market(2).Several analyses indicate that demand will eventually outpace production of these proteins.This imminent shortage has served to emphasize the need to improve on the yield that can be obtained from the systems currently in place.The majority of these proteins are produced in Chinese Hamster Ovary(CHO)cells,while the remainder are produced in a variety of other cell types including mouse myelomas NSO and SP2/0,baby hamster kidney(BHK)and a variety of others.CHO cells were first cultured in the late 1950's after their isolation from a Chinese hamster(Cricetulus griseus)ovary epithelial tumor(2).Produced in CHO,tPA was the first of these recombinant proteins to receive approval for therapeutic use in 1986(3).Many changes to the process have occurred since that time,including changes to the cells,the growth medium and the reactor conditions to improve from that first venture.
机译:从哺乳动物系统中制备治疗性重组蛋白是药物市场增长最快的部分之一(2)。多项分析表明,需求最终将超过这些蛋白的生产,这一迫在眉睫的短缺强调了提高产量的必要性。这些蛋白质的大部分是在中国仓鼠卵巢(CHO)细胞中产生的,而其余的则是在多种其他细胞类型中产生的,包括小鼠骨髓瘤NSO和SP2 / 0,婴儿仓鼠CHO细胞是在1950年代末从中国仓鼠卵巢上皮肿瘤中分离后首次培养的(2).CHO细胞是在CHO中产生的,tPA是第一个重组蛋白自1986年(3)获批准用于治疗以来。此后发生了许多过程变化,包括细胞,生长培养基和反应器条件的改善。从第一次冒险开始。

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