平移(音频)
生物信息学
单域抗体
表位
计算生物学
亲和力成熟
重组DNA
抗体
蛋白质工程
表位定位
抗原
生物
分子生物学
化学
生物化学
遗传学
酶
基因
缩放
古生物学
镜头(地质)
作者
Barbara Medagli,Miguel A. Soler,Rita De Zorzi,Sara Fortuna
标识
DOI:10.1007/978-1-0716-2609-2_19
摘要
Nanobodies (VHHs) are engineered fragments of the camelid single-chain immunoglobulins. The VHH domain contains the highly variable segments responsible for antigen recognition. VHHs can be easily produced as recombinant proteins. Their small size is a good advantage for in silico approaches. Computer methods represent a valuable strategy for the optimization and improvement of their binding affinity. They also allow for epitope selection offering the possibility to design new VHHs for regions of a target protein that are not naturally immunogenic. Here we present an in silico mutagenic protocol developed to improve the binding affinity of nanobodies together with the first step of their in vitro production. The method, already proven successful in improving the low Kd of a nanobody hit obtained by panning, can be employed for the ex novo design of antibody fragments against selected protein target epitopes.
科研通智能强力驱动
Strongly Powered by AbleSci AI