生物信息学
抗体
人源化抗体
互补决定区
生物
免疫球蛋白轻链
计算生物学
人性化鼠标
癌症研究
基因
免疫学
单克隆抗体
分子生物学
免疫系统
遗传学
作者
Haihui Yu,Ziyi Wang,Bowen Zhu,Ziheng Jia,Jing Luo,Han Xiao,Hui Chen,Rong Shao
标识
DOI:10.1016/j.bcp.2024.116335
摘要
Drugs specifically targeting YKL-40, an over-expressed gene (CHI3L1) in various diseases remain developed. The current study is to create a humanized anti-YKL-40 neutralizing antibody and characterize its potentially therapeutic signature. We utilized in silico CDR-grafting bioinformatics to replace the complementarity determining regions (CDRs) of human IgG1 with mouse CDRs of our previously established anti-YKL-40 antibody (mAY). In fifteen candidates (VL1-3/VH1-5) of heavy and light chain variable region combination, one antibody L3H4 named Rosazumab demonstrated strong binding affinity with YKL-40 (K
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