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基于肽的PDZ结构域抑制剂的开发。

Development of Peptide-Based PDZ Domain Inhibitors.

作者信息

Essig Dominik J, Balboa Javier R, Strømgaard Kristian

机构信息

Department of Drug Design and Pharmacology, Center for Biopharmaceuticals, University of Copenhagen, Copenhagen, Denmark.

Novo Nordisk A/S, Research Chemistry 3, Måløv, Denmark.

出版信息

Methods Mol Biol. 2021;2256:157-177. doi: 10.1007/978-1-0716-1166-1_10.

Abstract

Over the past decades, peptide-based drugs have gained increasing interest in a wide range of treatment applications, primarily because of high potency and selectivity, as well as good efficacy, tolerability, and safety often achieved with peptides. Attempts to target postsynaptic density protein of 95 (PSD-95) PSD-95/Discs large/Zonula occludens-1 (PDZ) domains, which mediate the formation of a ternary complex with the N-methyl-D-aspartate (NMDA) receptor and neuronal nitric oxide synthase (nNOS) responsible for excitotoxicity in ischemic stroke, by high-affinity small molecules have failed in the past. In this chapter, we focus on the discovery of peptide-based drugs targeting PSD-95, using AVLX-144 as an example, from the synthesis, over binding assays to its target, to further in vitro experiments based on the development of AVLX-144, a potential stroke treatment, which is planned to enter clinical trials in 2020.

摘要

在过去几十年中,基于肽的药物在广泛的治疗应用中越来越受到关注,主要是因为肽通常具有高效能、高选择性,以及良好的疗效、耐受性和安全性。过去,试图通过高亲和力小分子靶向95kDa突触后致密蛋白(PSD-95)的PSD-95/盘状大蛋白/闭合蛋白-1(PDZ)结构域的尝试均告失败,该结构域介导与N-甲基-D-天冬氨酸(NMDA)受体和神经元型一氧化氮合酶(nNOS)形成三元复合物,而这两种物质在缺血性中风中会导致兴奋性毒性。在本章中,我们以AVLX-144为例,重点介绍基于肽的靶向PSD-95药物的发现过程,内容涵盖从合成、与靶点的结合试验,到基于AVLX-144开展的进一步体外实验,AVLX-144是一种潜在的中风治疗药物,计划于2020年进入临床试验。

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