蛋白质G
化学
抗体
蛋白质A/G
蛋白质A
碎片结晶区
结合蛋白
融合蛋白
绑定域
生物化学
结合位点
生物
受体
免疫学
重组DNA
基因
作者
Lixia Hu,Rongrong Wang,Qinxue Wu,Yan Wan,Yifeng Li
出处
期刊:Protein and Peptide Letters
[Bentham Science]
日期:2024-08-16
卷期号:31
被引量:2
标识
DOI:10.2174/0109298665320125240805112024
摘要
Protein A resins have been widely used for product capture during mAb, bispecific antibody (bsAb), and Fc-fusion protein purification. While Protein A ligands mainly bind the Fc region, many of them can also bind the VH3 domain. During mAb/bsAb purification, certain truncated byproducts may contain the same Fc region as the product but fewer numbers of the VH3 domain. In such a scenario, VH3-binding Protein A resins provide a potential means for byproduct separation based on the difference in VH3-binding valency. As the ligands of different VH3-binding Protein A resins are derived from distinct domains of the native Protein A, it would be interesting to know whether they possess comparable capabilities for separating species with the same Fc region but different numbers of VH3 domain.
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