蛋白酵素
蛋白酶
组织蛋白酶B
分子生物学
半胱氨酸蛋白酶
NS2-3蛋白酶
生物化学
组织蛋白酶
碎片(计算)
组织蛋白酶L
化学
生物
丝氨酸蛋白酶
酶
生态学
作者
Lixia Hu,Shanshan Liu,Lisha Xia,Xiaoji Cong,Xu Chu,Li Wang,Yifeng Li
标识
DOI:10.1016/j.pep.2022.106144
摘要
In a previous work we demonstrated that CHO protease caused fragmentation of an expressed bispecific antibody (bsAb) and this detrimental host cell protein (HCP) can be effectively removed through an optimized Protein A wash step. In addition, preliminary evidence suggested that the responsible protease belongs to the threonine or cysteine protease family. In the current study, this protease was further identified as cathepsin B. First, we identified several CHO proteases in the further fractionated Protein A wash using liquid chromatography-tandem mass spectrometry (LC-MS/MS), and this allowed us to select four candidate proteases. Next, by examining the cleavage pattern of each individual protease and comparing it with that observed during purification, cathepsin B was identified as the protease responsible for the observed bsAb fragmentation.
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