Hamzeh-Mivehroud Maryam, Alizadeh Ali Akbar, Morris Michael B, Church W Bret, Dastmalchi Siavoush
Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; School of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Drug Discov Today. 2013 Dec;18(23-24):1144-57. doi: 10.1016/j.drudis.2013.09.001. Epub 2013 Sep 17.
Phage display represents an important approach in the development pipeline for producing peptides and peptidomimetics therapeutics. Using randomly generated DNA sequences and molecular biology techniques, large diverse peptide libraries can be displayed on the phage surface. The phage library can be incubated with a target of interest and the phage which bind can be isolated and sequenced to reveal the displayed peptides' primary structure. In this review, we focus on the 'mechanics' of the phage display process, whilst highlighting many diverse and subtle ways it has been used to further the drug-development process, including the potential for the phage particle itself to be used as a drug carrier targeted to a particular pathogen or cell type in the body.
噬菌体展示是生产肽和肽模拟物疗法开发流程中的一种重要方法。利用随机生成的DNA序列和分子生物学技术,可以在噬菌体表面展示大量多样的肽库。可以将噬菌体文库与感兴趣的靶标一起孵育,然后分离并测序结合的噬菌体,以揭示所展示肽的一级结构。在本综述中,我们关注噬菌体展示过程的“机制”,同时强调它在推进药物开发过程中被使用的多种不同且微妙的方式,包括噬菌体颗粒本身用作靶向体内特定病原体或细胞类型的药物载体的潜力。