Technology and Process Development (TPD), WuXi Biologics, 288 Fute Zhong Road, Waigaoqiao Free Trade Zone, Shanghai, 200131, China.
,Analytical Sciences (AS), WuXi Biologics, 288 Fute Zhong Road, Waigaoqiao Free Trade Zone, Shanghai, 200131, China.
Protein Expr Purif. 2022 Nov;199:106144. doi: 10.1016/j.pep.2022.106144. Epub 2022 Jul 13.
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.
在之前的工作中,我们证明 CHO 蛋白酶会导致表达的双特异性抗体(bsAb)发生片段化,而这种有害的宿主细胞蛋白(HCP)可以通过优化的 Protein A 洗涤步骤有效去除。此外,初步证据表明,负责该过程的蛋白酶属于苏氨酸或半胱氨酸蛋白酶家族。在本研究中,该蛋白酶进一步被鉴定为组织蛋白酶 B。首先,我们使用液相色谱-串联质谱法(LC-MS/MS)在进一步分馏的 Protein A 洗涤液中鉴定了几种 CHO 蛋白酶,这使我们能够选择四种候选蛋白酶。接下来,通过检查每种蛋白酶的切割模式,并将其与纯化过程中观察到的切割模式进行比较,鉴定出组织蛋白酶 B 是导致观察到的 bsAb 片段化的蛋白酶。