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自然学派:配体非依赖性免疫调节肽。

SCHOOL of nature: ligand-independent immunomodulatory peptides.

机构信息

SignaBlok, Inc., Shrewsbury, MA, USA.

出版信息

Drug Discov Today. 2020 Aug;25(8):1298-1306. doi: 10.1016/j.drudis.2020.05.005. Epub 2020 May 12.

Abstract

Groundbreaking studies in protein biophysics have identified the mechanisms of transmembrane signaling at the level of druggable protein-protein interactions (PPIs). This resulted in the development of the signaling chain homooligomerization (SCHOOL) strategy to modulate cell responses using receptor-specific peptides. Inspired by nature, these short peptides use ligand-independent mechanisms of receptor inhibition and demonstrate potent efficacy in vitro and in vivo. The SCHOOL strategy is especially important when receptor ligands are unknown. An example is the triggering receptor expressed on myeloid cells-1 (TREM-1) receptor, an emerging therapeutic target involved in the pathogenesis of most inflammatory diseases. Here, I discuss advances in the field with a focus on TREM-1 inhibitory SCHOOL peptides that offer new hope for a 'magic bullet' cure for cancer, arthritis, sepsis, retinopathy, and other medical challenges.

摘要

开创性的蛋白质生物物理学研究已经确定了可药物结合的蛋白质-蛋白质相互作用(PPIs)水平的跨膜信号转导机制。这导致了信号链同源寡聚化(SCHOOL)策略的发展,该策略使用受体特异性肽来调节细胞反应。受自然启发,这些短肽使用受体抑制的配体独立机制,并在体外和体内显示出强大的疗效。当受体配体未知时,SCHOOL 策略尤为重要。触发受体表达在髓样细胞上-1(TREM-1)受体就是一个例子,它是一种新兴的治疗靶点,参与大多数炎症性疾病的发病机制。在这里,我将重点讨论该领域的进展,包括 TREM-1 抑制性 SCHOOL 肽,为癌症、关节炎、败血症、视网膜病变和其他医学挑战的“灵丹妙药”提供了新的希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1238/7217646/72b9ef54cb1d/fx1_lrg.jpg

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