计算生物学
药物发现
鉴定(生物学)
DNA
DNA测序
计算机科学
小分子
生物
纳米技术
数据科学
组合化学
化学
生物信息学
遗传学
材料科学
植物
作者
Daniel H. Madsen,Carlos Azevedo,Iolanda Micco,L. Petersen,Nils Jakob Vest Hansen
出处
期刊:Progress in Medicinal Chemistry
[Elsevier BV]
日期:2020-01-01
卷期号:: 181-249
被引量:53
标识
DOI:10.1016/bs.pmch.2020.03.001
摘要
DNA-encoded libraries (DELs) are collections of small molecules covalently attached to amplifiable DNA tags carrying unique information about the structure of each library member. A combinatorial approach is used to construct the libraries with iterative DNA encoding steps, facilitating tracking of the synthetic history of the attached compounds by DNA sequencing. Various screening protocols have been developed which allow protein target binders to be selected out of pools containing up to billions of different small molecules. The versatile methodology has allowed identification of numerous biologically active compounds and is now increasingly being adopted as a tool for lead discovery campaigns and identification of chemical probes. A great focus in recent years has been on developing DNA compatible chemistries that expand the structural diversity of the small molecule library members in DELs. This chapter provides an overview of the challenges and accomplishments in DEL technology, reviewing the technological aspects of producing and screening DELs with a perspective on opportunities, limitations, and future directions.
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