药物发现
计算生物学
药品
单克隆抗体
整体膜蛋白
化学
膜
生物化学
膜蛋白
药理学
医学
药物开发
生物
计算机科学
生物信息学
抗体
免疫学
作者
Ellen Gulezian,Christina Crivello,Janna Bednenko,Claudia Zafra,Yihui Zhang,Paul A. Colussi,Sunyia Hussain
标识
DOI:10.1016/j.tips.2021.05.006
摘要
Integral membrane proteins (MPs) are important drug targets across most fields of medicine, but historically have posed a major challenge for drug discovery due to difficulties in producing them in functional forms. We review the state of the art in drug discovery strategies using recombinant multipass MPs, and outline methods to successfully express, stabilize, and formulate them for small-molecule and monoclonal antibody therapeutics development. Advances in structure-based drug design and high-throughput screening are allowing access to previously intractable targets such as ion channels and transporters, propelling the field towards the development of highly specific therapies targeting desired conformations.
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