中国仓鼠卵巢细胞
蛋白质水解
蛋白酶
细胞生物学
重组DNA
生物
融合蛋白
丝氨酸蛋白酶
生物制药
跨膜蛋白
化学
蛋白质降解
生物化学
金属蛋白酶
激活剂(遗传学)
转染
细胞培养
蛋白酶体
靶蛋白
毛茛
分子生物学
膜蛋白
抗体
肠肽酶
蛋白水解酶
丝氨酸
作者
Qinghao Zhang,Fnu Aapjeet,Joyce Chen,Xiaoyan Tang,Gregory F. Pirrone,Alexey A. Makarov,Fengfei Ma,Luke Nelson,Jessica Pan,Ren Liu,Michael J. Hohn,David J. Busch
摘要
Proteolytic degradation of recombinant proteins in Chinese hamster ovary (CHO) cells remains a major challenge in biopharmaceutical manufacturing, often reducing product yield and quality. Matriptase-1, a type II transmembrane serine protease, has been identified as a key contributor to unwanted proteolysis. This study investigates hepatocyte growth factor activator inhibitor-1 (HAI-1) overexpression as a strategy to mitigate matriptase-1-mediated degradation in CHO cell culture. Using an IL-12 IgG1 Fc fusion protein and a multi-specific antibody (M molecule) as model proteins, we employed genetic and biochemical approaches to assess the impact of Chinese hamster HAI-1 overexpression on protein quality and yield. Our results demonstrate that HAI-1 overexpression effectively inhibits matriptase-1 activity, achieving up to a 98% reduction in proteolytic clipping while maintaining cell growth, viability, and product quality. Compared to other protease control strategies, HAI-1 overexpression presents a practical and scalable solution that does not disrupt essential cellular functions. These findings establish HAI-1 as a key modulatory tool in CHO-based protein production, with implications for reducing proteolysis of therapeutic proteins and optimizing biopharmaceutical manufacturing processes.
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