化学
亲和层析
色谱法
dBc公司
配体(生物化学)
蛋白质工程
重组DNA
蛋白质A
抗体
生物化学
酶
受体
基因
光学
物理
相位噪声
生物
免疫学
作者
Saman Rahmati,Fatemeh Torkashvand,Massoud Amanlou,Kowsar Bagherzadeh,Pezhman Fard Esfahani,Hooman Aghamirza Moghim Aliabadi,Behrouz Vaziri
标识
DOI:10.1021/acs.analchem.1c01871
摘要
Protein L affinity chromatography is a useful method for the purification of antibody fragments containing kappa light chains. In affinity chromatography, increasing the binding affinity leads to increased product purity, recovery, and dynamic binding capacity (DBC). In this study, molecular docking and molecular dynamics simulation techniques were used to design the engineered Protein L with higher affinity to the kappa light chain. Each engineered ligand was produced as a recombinant protein and coupled to a solid matrix. The purity, recovery, and DBC of the engineered resins were evaluated and then compared to those of a commercially available resin. The results showed important parameters for engineering more efficient Protein L ligands for affinity chromatography.
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