Feng Zhaoqianqi, Xu Bing
Biomol Concepts. 2016 Jun 1;7(3):179-87. doi: 10.1515/bmc-2015-0035.
D-amino acids, the enantiomers of naturally abundant L-amino acids, bear unique stereochemistry properties that lead to the resistance towards most of the endogenous enzymes. Previous works have demonstrated applications of D-amino acids in therapeutic development with the aid of mirror-image phage display and retro-inverso peptide synthesis. In this review, we highlight the recent progress and challenges in the exploration of D-amino acids at the interface of chemistry and life science. First, we will introduce some progress made in traditional application of D-amino acids to enhance biostability of peptide therapeutics. Then, we discuss some works that explore the relatively underexplored interactions between the enzyme and D-amino acids and enzymatic reactions of D-amino acids. To highlight the enzymatic reactions of D-amino acids, we will describe several emerging works on the enzyme-instructed self-assembly (EISA) and their potential application in selective anti-inflammatory or anticancer therapies. At the end, we briefly mention the challenges and possible future directions.
D-氨基酸是天然丰富的L-氨基酸的对映体,具有独特的立体化学性质,使其对大多数内源性酶具有抗性。先前的研究已经证明了D-氨基酸在镜像噬菌体展示和逆反转肽合成的辅助下在治疗开发中的应用。在这篇综述中,我们重点介绍了在化学与生命科学交叉领域探索D-氨基酸的最新进展和挑战。首先,我们将介绍D-氨基酸在增强肽类治疗药物生物稳定性的传统应用方面取得的一些进展。然后,我们讨论一些探索酶与D-氨基酸之间相对未充分研究的相互作用以及D-氨基酸的酶促反应的研究工作。为了突出D-氨基酸的酶促反应,我们将描述一些关于酶指导的自组装(EISA)的新兴研究及其在选择性抗炎或抗癌治疗中的潜在应用。最后,我们简要提及挑战和可能的未来方向。