工具箱
药物发现
肽
氨基酸
计算机科学
计算生物学
符号
化学
组合化学
生物化学
生物
数学
程序设计语言
算术
作者
Jennifer L. Hickey,Daniel Sindhikara,Susan L. Zultanski,Danielle M. Schultz
标识
DOI:10.1021/acsmedchemlett.3c00037
摘要
Life is constructed primarily using a toolbox of 20 canonical amino acids─relying upon these building blocks for the assembly of proteins and peptides that regulate nearly every cellular task, including cell structure, function, and maintenance. While Nature continues to be a source of inspiration for drug discovery, medicinal chemists are not beholden to only 20 canonical amino acids and have begun to explore non-canonical amino acids (ncAAs) for the construction of designer peptides with improved drug-like properties. However, as our toolbox of ncAAs expands, drug hunters are encountering new challenges in approaching the iterative peptide design–make–test–analyze cycle with a seemingly boundless set of building blocks. This Microperspective focuses on new technologies that are accelerating ncAA interrogation in peptide drug discovery (including HELM notation, late-stage functionalization, and biocatalysis) while shedding light on areas where further investment could not only accelerate the discovery of new medicines but also improve downstream development.
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