点突变
突变体
亲和力成熟
计算生物学
突变
抗体
氢键
遗传学
生物
化学
基因
分子
有机化学
作者
Shuntaro Chiba,Yasushi Okuno,Masateru Ohta
标识
DOI:10.1007/978-1-0716-2609-2_18
摘要
Structure-based site-directed affinity maturation of antibodies can be expanded by multiple-point mutations to obtain various mutants. However, selecting the appropriate number of promising mutants for experimental evaluation from the vast number of combinations of multiple-point mutations is challenging. In this report, we describe how to narrow candidate mutants using the so-called weak interaction analysis such as CH–π and CH–O in addition to widely recognized interactions such as hydrogen bonds.
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