平移(音频)
噬菌体展示
噬菌体
单域抗体
生物
计算生物学
单克隆抗体
抗原
抗体
分子生物学
遗传学
噬菌体
基因
大肠杆菌
缩放
古生物学
镜头(地质)
作者
Callum Joyce,Louise Speight,Alastair D. G. Lawson,Anthony Scott-Tucker,Alex Macpherson
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 83-97
被引量:1
标识
DOI:10.1007/978-1-0716-3279-6_6
摘要
Phage display is an in vitro technique used in the discovery of monoclonal antibodies that has been used successfully in the discovery of both camelid VHH and shark variable new antigen receptor domains (VNAR). Bovines also contain a unique "ultralong CDRH3" with a conserved structural motif, comprising a knob domain and β-stalk. When removed from the antibody scaffold, either the entire ultralong CDRH3 or the knob domain alone, is typically capable of binding an antigen, to produce antibody fragments that are smaller than both VHH and VNAR. By extracting immune material from bovine animals and specifically amplifying knob domain DNA sequences by PCR, knob domain sequences can be cloned into a phagemid vector producing knob domain phage libraries. Target-specific knob domains can be enriched by panning the libraries against an antigen of interest. Phage display of knob domains exploits the link between phage genotype and phenotype and could prove to be a high throughput method to discover target-specific knob domains, helping to explore the pharmacological properties of this unique antibody fragment.
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