药物发现
小分子
支柱
计算生物学
纳米技术
计算机科学
对偶(语法数字)
组合化学
化学
材料科学
生物
工程类
生物化学
结构工程
文学类
艺术
作者
Alice Lessing,Dimitar Petrov,Jörg Scheuermann
标识
DOI:10.1016/j.tips.2023.08.006
摘要
DNA-encoded chemical library technology (DECL or DEL) has become an important pillar for small-molecule drug discovery. The technology rapidly identifies small-molecule hits for relevant target proteins at low cost and with a high success rate, including ligands for targeted protein degradation (TPD). More recently, the setup of DNA- or peptide nucleic acid (PNA)-encoded chemical libraries based on the simultaneous display of ligand pairs, termed dual-display, allows for more sophisticated applications which will be reviewed herein. Both stable and dynamic dual-display DEL technologies enable innovative affinity-based selection modalities, even on and in cells. Novel methods for a seamless conversion between single- and double-stranded library formats allow for even more versatility. We present the first candidates emerging from dual-display technologies and discuss the future potential of dual-display for drug discovery.
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