噬菌体展示
表位
肽库
单链
化学
平移(音频)
抗体
分子生物学
生物
功能(生物学)
噬菌体
计算生物学
细胞生物学
肽序列
噬菌体
生物化学
基因
大肠杆菌
遗传学
缩放
古生物学
镜头(地质)
作者
Steffen U. Eisenhardt,Meike Schwarz,Nicole Bassler,Karlheinz Peter
出处
期刊:Nature Protocols
[Springer Nature]
日期:2007-11-21
卷期号:2 (12): 3063-3073
被引量:70
标识
DOI:10.1038/nprot.2007.455
摘要
Phage-display of antibody libraries is a powerful tool to select antibodies for specific epitopes. We describe a strategy for selecting highly specific scFv-clones that discriminate between various conformational states of cell surface receptors. This approach adapts the M13 pIII phage-display technology toward a cell suspension-based strategy, which allows panning against complex, multimeric, fully functional cell membrane epitopes without alteration of structure due to purification or immobilization. As the functional properties are preserved, phage can be specifically depleted or selected for neo-epitopes exposed after physiological alterations of the targeted molecules. This subtractive strategy allows highly specific selection for single-chain antibodies directed against functionally regulated epitopes on the cell surface molecules that can be tailored for diagnostic and therapeutic applications. Using this protocol, activation-specific single-chain antibodies can be obtained within 4-6 weeks.
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