Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
Angew Chem Int Ed Engl. 2013 Jul 8;52(28):7098-124. doi: 10.1002/anie.201208344. Epub 2013 May 31.
Freestanding nonproteinogenic amino acids have long been recognized for their antimetabolite properties and tendency to be uncovered to reactive functionalities by the catalytic action of target enzymes. By installing them regiospecifically into biogenic peptides and proteins, it may be possible to usher a new era at the interface between small molecule and large molecule medicinal chemistry. Site-selective protein functionalization offers uniquely attractive strategies for posttranslational modification of proteins. Last, but not least, many of the amino acids not selected by nature for protein incorporation offer rich architectural possibilities in the context of ribosomally derived polypeptides. This Review summarizes the biosynthetic routes to and metabolic logic for the major classes of the noncanonical amino acid building blocks that end up in both nonribosomal peptide frameworks and in hybrid nonribosomal peptide-polyketide scaffolds.
非天然存在的氨基酸很早就因其抗代谢物特性以及被靶酶的催化作用暴露于反应性功能基团的倾向而受到关注。通过将它们区域特异性地引入生物源肽和蛋白质中,有可能在小分子和大分子药物化学的界面上开创一个新时代。定点蛋白质功能化提供了用于蛋白质翻译后修饰的极具吸引力的策略。最后但同样重要的是,自然界中没有被选择用于蛋白质掺入的许多氨基酸在核糖体衍生多肽的背景下提供了丰富的结构可能性。本综述总结了非典型氨基酸构建块的生物合成途径和代谢逻辑,这些构建块最终存在于非核糖体肽框架和混合非核糖体肽-聚酮骨架中。