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趋化因子受体的变构抑制剂:机遇与陷阱

Allosteric inhibitors of chemoattractant receptors: opportunities and pitfalls.

作者信息

Allegretti Marcello, Bertini Riccardo, Bizzarri Cinzia, Beccari Andrea, Mantovani Alberto, Locati Massimo

机构信息

Research Center, Dompé pha.r.ma s.p.a., I-67100 L'Aquila, Italy.

出版信息

Trends Pharmacol Sci. 2008 Jun;29(6):280-6. doi: 10.1016/j.tips.2008.03.005. Epub 2008 Apr 20.

Abstract

Given the central role of chemokines in infection, inflammation and immunity, chemokine receptors are a prime target for pharmacological intervention, and more so after the recent approval of chemokine receptor inhibitors for HIV. Allosteric inhibitors offer a largely unexploited opportunity to interfere with and modulate chemokine receptor activation and signaling. In addition to characterizing binding mode as a first step to understanding the specific mechanism underlying drug action, allosteric inhibitors pose new questions concerning different phases in drug discovery and pharmacological characterization, including the identification of appropriate screening tests, the evaluation of inhibitory effects on different signaling pathways and the implications of agonist- and signaling pathway-dependent inhibition for overall in vivo efficacy.

摘要

鉴于趋化因子在感染、炎症和免疫中发挥的核心作用,趋化因子受体是药物干预的主要靶点,尤其是在趋化因子受体抑制剂最近获批用于治疗HIV之后。变构抑制剂为干扰和调节趋化因子受体激活及信号传导提供了一个很大程度上未被开发利用的机会。除了将结合模式作为理解药物作用具体机制的第一步进行表征外,变构抑制剂还在药物发现和药理学表征的不同阶段提出了新问题,包括确定合适的筛选试验、评估对不同信号通路的抑制作用以及激动剂和信号通路依赖性抑制对整体体内疗效的影响。

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