互补决定区
肽库
抗体
半抗原
计算生物学
大肠杆菌
噬菌体展示
组合化学
互补性(分子生物学)
寡核苷酸
定向进化
化学
免疫球蛋白轻链
生物
遗传学
生物化学
DNA
基因
肽序列
突变体
作者
Carlos F. Barbas,Jim D. Bain,Denise Hoekstra,R.A. Lerner
标识
DOI:10.1073/pnas.89.10.4457
摘要
The properties of naiveté and large diversity are considered to be essential starting features for combinatorial antibody libraries that eschew immunization by evolution in vitro. We have prepared large libraries with such properties by using random oligonucleotide synthesis, which has the potential to create approximately 10(20) complementarity-determining regions for antibody heavy chains. When combined with light chains and expressed on phage surfaces, high-affinity antibodies could be selected from 5.0 x 10(7) Escherichia coli transformants. Remarkably, antibodies selected only for binding displayed both general structural features known to be important in nature's own antibodies and specific consensus sequences thought to be critical for interaction with the hapten against which the library was selected. Semisynthetic and ultimately totally synthetic combinatorial libraries when coupled with mutation and selection procedures should replace immunization for generation of reagent, therapeutic, and catalytic antibodies.
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