Department of Pharmaceutical Chemistry and the Cardiovascular Research Institute, University of California, San Francisco, CA 94158, United States.
Department of Pharmaceutical Chemistry and the Cardiovascular Research Institute, University of California, San Francisco, CA 94158, United States.
Bioorg Med Chem. 2021 Jan 1;29:115896. doi: 10.1016/j.bmc.2020.115896. Epub 2020 Nov 26.
Drugs with a covalent mechanism of action benefit from enhanced potency, selectivity, and in vivo efficacy. Historically, the only covalent drugs on the market have been covalent small molecules. However, many proteins and protein-protein interactions cannot be targeted by small molecules due to their lack of small molecule binding pockets, and are thus deemed "undruggable." In order to drug the undruggable, peptide and protein therapeutics that can better bind to flat protein surfaces have been developed. Until recently, peptide and protein therapeutics have had noncovalent mechanisms of action. The recent advancement of unnatural amino acid chemistry, along with the development of better and more specific electrophilic warheads, has allowed for the application of covalent mechanisms to peptide and protein drugs. Covalent peptide and protein therapeutics have the potential to benefit from the same advantages that covalent small molecules have over their noncovalent counterparts. Here we provide a brief overview of the chemistry that makes this advancement possible, as well as examples of covalent peptides and the first covalent protein drug. These examples successfully crosslink their target proteins and have beneficial therapeutic effects.
具有共价作用机制的药物受益于增强的效力、选择性和体内功效。从历史上看,市场上仅有的共价药物是共价小分子。然而,由于缺乏小分子结合口袋,许多蛋白质和蛋白质-蛋白质相互作用不能被小分子靶向,因此被认为是“不可成药的”。为了对这些“不可成药的”靶点进行药物治疗,已经开发了能够更好地结合平坦蛋白质表面的肽和蛋白质治疗药物。直到最近,肽和蛋白质治疗药物才具有非共价作用机制。非天然氨基酸化学的最新进展,以及更好、更特异的亲电弹头的开发,使得共价机制能够应用于肽和蛋白质药物。共价肽和蛋白质治疗药物有可能受益于共价小分子相对于非共价类似物的相同优势。在这里,我们简要概述了实现这一进展的化学原理,以及共价肽的实例和第一个共价蛋白质药物。这些实例成功地交联了它们的靶蛋白,并具有有益的治疗效果。