Department of Chemistry and the State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China.
Laboratory for Synthetic Chemistry and Chemical Biology Limited, Health@InnoHK, Innovation and Technology Commission, Units 1503-1511, 15/F., Building 17W, Hong Kong Science and Technology Parks, New Territories, Hong Kong SAR, China.
Chembiochem. 2021 Jul 15;22(14):2384-2397. doi: 10.1002/cbic.202100144. Epub 2021 May 7.
DNA-encoded libraries (DEL) have come of age and become a major technology platform for ligand discovery in both academia and the pharmaceutical industry. Technological maturation in the past two decades and the recent explosive developments of DEL-compatible chemistries have greatly improved the chemical diversity of DELs and fueled its applications in drug discovery. A relatively less-covered aspect of DELs is the selection method. Typically, DEL selection is considered as a binding assay and the selection is conducted with purified protein targets immobilized on a matrix, and the binders are separated from the non-binding background via physical washes. However, the recent innovations in DEL selection methods have not only expanded the target scope of DELs, but also revealed the potential of the DEL technology as a powerful tool in exploring fundamental biology. In this Review, we first cover the "classic" DEL selection methods with purified proteins on solid phase, and then we discuss the strategies to realize DEL selections in solution phase. Finally, we focus on the emerging approaches for DELs to interrogate complex biological targets.
DNA 编码文库 (DEL) 已经成熟,成为学术界和制药行业配体发现的主要技术平台。在过去的二十年中,技术的成熟和最近 DEL 兼容化学的爆炸式发展极大地提高了 DEL 的化学多样性,并推动了其在药物发现中的应用。DEL 的一个相对较少被关注的方面是选择方法。通常,DEL 选择被认为是一种结合测定法,并且使用固定在基质上的纯化蛋白靶标进行选择,并且通过物理洗涤将结合物与非结合背景分离。然而,最近 DEL 选择方法的创新不仅扩展了 DEL 的靶标范围,而且还揭示了 DEL 技术作为探索基础生物学的强大工具的潜力。在这篇综述中,我们首先介绍固相纯化蛋白的“经典”DEL 选择方法,然后讨论在溶液相中实现 DEL 选择的策略。最后,我们重点介绍 DEL 用于研究复杂生物靶标的新兴方法。