Fan Yu, Feng Ruibing, Zhang Xinya, Wang Zhen-Liang, Xiong Feng, Zhang Shuihua, Zhong Zhang-Feng, Yu Hua, Zhang Qing-Wen, Zhang Zhang, Wang Yitao, Li Guodong
Macao Centre for Research and Development in Chinese Medicine, State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao SAR 999078, China.
State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao SAR 999078, China.
Acta Pharm Sin B. 2024 Aug;14(8):3362-3384. doi: 10.1016/j.apsb.2024.04.006. Epub 2024 Apr 10.
Drug discovery is a sophisticated process that incorporates scientific innovations and cutting-edge technologies. Compared to traditional bioactivity-based screening methods, encoding and display technologies for combinatorial libraries have recently advanced from proof-of-principle experiments to promising tools for pharmaceutical hit discovery due to their high screening efficiency, throughput, and resource minimization. This review systematically summarizes the development history, typology, and prospective applications of encoding and displayed technologies, including phage display, ribosomal display, mRNA display, yeast cell display, one-bead one-compound, DNA-encoded, peptide nucleic acid-encoded, and new peptide-encoded technologies, and examples of preclinical and clinical translation. We discuss the progress of novel targeted therapeutic agents, covering a spectrum from small-molecule inhibitors and nonpeptidic macrocycles to linear, monocyclic, and bicyclic peptides, in addition to antibodies. We also address the pending challenges and future prospects of drug discovery, including the size of screening libraries, advantages and disadvantages of the technology, clinical translational potential, and market space. This review is intended to establish a comprehensive high-throughput drug discovery strategy for scientific researchers and clinical drug developers.
药物发现是一个复杂的过程,它融合了科学创新和前沿技术。与传统的基于生物活性的筛选方法相比,组合文库的编码和展示技术由于其高筛选效率、通量和资源最小化,最近已从原理验证实验发展成为药物先导物发现的有前景的工具。本文系统总结了编码和展示技术的发展历史、类型及潜在应用,包括噬菌体展示、核糖体展示、mRNA展示、酵母细胞展示、一珠一化合物、DNA编码、肽核酸编码和新型肽编码技术,以及临床前和临床转化的实例。我们讨论了新型靶向治疗药物的进展,涵盖从小分子抑制剂、非肽大环化合物到线性、单环和双环肽,以及抗体。我们还探讨了药物发现面临的挑战和未来前景,包括筛选文库的规模、技术的优缺点、临床转化潜力和市场空间。本文旨在为科研人员和临床药物开发者建立一个全面的高通量药物发现策略。