单克隆抗体
整体膜蛋白
膜蛋白
药物发现
跨膜蛋白
计算生物学
抗体
脂质双层
抗原
生物
化学
细胞生物学
受体
生物化学
膜
免疫学
作者
Roger B. Dodd,Darren J. Schofield,Trevor Wilkinson,Zachary T. Britton
出处
期刊:Methods
[Elsevier]
日期:2020-05-15
卷期号:180: 111-126
被引量:15
标识
DOI:10.1016/j.ymeth.2020.05.006
摘要
Complex integral membrane proteins, which are embedded in the cell surface lipid bilayer by multiple transmembrane spanning helices, encompass families of proteins which are important target classes for drug discovery. These protein families include G protein-coupled receptors, ion channels and transporters. Although these proteins have typically been targeted by small molecule drugs and peptides, the high specificity of monoclonal antibodies offers a significant opportunity to selectively modulate these target proteins. However, it remains the case that isolation of antibodies with desired pharmacological function(s) has proven difficult due to technical challenges in preparing membrane protein antigens suitable to support antibody drug discovery. In this review recent progress in defining strategies for generation of membrane protein antigens is outlined. We also highlight antibody isolation strategies which have generated antibodies which bind the membrane protein and modulate the protein function.
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