计算生物学
表位
结构生物学
噬菌体展示
重组DNA
蛋白质工程
生物
抗原
细胞生物学
抗体
生物化学
基因
遗传学
酶
作者
Els Pardon,Toon Laeremans,Sarah Triest,Søren G. F. Rasmussen,Alexandre Wohlkönig,A. Ruf,Serge Muyldermans,Wim G. J. Hol,Brian K. Kobilka,Jan Steyaert
出处
期刊:Nature Protocols
[Springer Nature]
日期:2014-02-27
卷期号:9 (3): 674-693
被引量:649
标识
DOI:10.1038/nprot.2014.039
摘要
There is growing interest in using antibodies as auxiliary tools to crystallize proteins. Here we describe a general protocol for the generation of Nanobodies to be used as crystallization chaperones for the structural investigation of diverse conformational states of flexible (membrane) proteins and complexes thereof. Our technology has a competitive advantage over other recombinant crystallization chaperones in that we fully exploit the natural humoral response against native antigens. Accordingly, we provide detailed protocols for the immunization with native proteins and for the selection by phage display of in vivo–matured Nanobodies that bind conformational epitopes of functional proteins. Three representative examples illustrate that the outlined procedures are robust, making it possible to solve by Nanobody-assisted X-ray crystallography in a time span of 6–12 months.
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