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缺氧诱导因子(HIF)作为研究蛋白质-蛋白质相互作用抑制的模型。

Hypoxia inducible factor (HIF) as a model for studying inhibition of protein-protein interactions.

作者信息

Burslem George M, Kyle Hannah F, Nelson Adam, Edwards Thomas A, Wilson Andrew J

机构信息

School of Chemistry , University of Leeds , Woodhouse Lane , Leeds LS2 9JT , UK . Email:

Astbury Centre for Structural Molecular Biology , University of Leeds , Woodhouse Lane , Leeds LS2 9JT , UK.

出版信息

Chem Sci. 2017 Jun 1;8(6):4188-4202. doi: 10.1039/c7sc00388a. Epub 2017 Apr 26.

Abstract

The modulation of protein-protein interactions (PPIs) represents a major challenge in modern chemical biology. Current approaches ( high-throughput screening, computer aided ligand design) are recognised as having limitations in terms of identification of hit matter. Considerable success has been achieved in terms of developing new approaches to PPI modulator discovery using the p53/DM2 and Bcl-2 family of PPIs. However these important targets in oncology might be considered as "low-hanging-fruit". Hypoxia inducible factor (HIF) is an emerging, but not yet fully validated target for cancer chemotherapy. Its role is to regulate the hypoxic response and it does so through a plethora of protein-protein interactions of varying topology, topography and complexity: its modulation represents an attractive approach to prevent development of new vasculature by hypoxic tumours.

摘要

蛋白质-蛋白质相互作用(PPI)的调控是现代化化学生物学面临的一项重大挑战。目前的方法(高通量筛选、计算机辅助配体设计)在命中物质的识别方面存在局限性,这已得到公认。在开发利用p53/DM2和Bcl-2家族PPI发现PPI调节剂的新方法方面已经取得了相当大的成功。然而,肿瘤学中的这些重要靶点可能被视为“低垂的果实”。缺氧诱导因子(HIF)是癌症化疗中一个新兴但尚未完全验证的靶点。它的作用是调节缺氧反应,并且通过大量拓扑结构、形貌和复杂性各异的蛋白质-蛋白质相互作用来实现这一点:对其进行调控是一种有吸引力的方法,可用于阻止缺氧肿瘤形成新的脉管系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d5/5576430/a07afd98d710/c7sc00388a-f1.jpg

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