细胞外蛋白的无偏鉴定-蛋白相互作用的药物靶点和生物药物发现

Shengya Cao, N. Martinez-Martin
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引用次数: 3

摘要

无偏筛选技术的进步加速了药物靶点的发现。特别是,膜嵌入和分泌蛋白因其协调细胞间通讯的能力而受到关注。它们的细胞外蛋白-蛋白相互作用(ePPIs)的失调是许多人类疾病的发生和发展的基础。实际上,由于eppi在质膜外起作用,因此也可以通过治疗药物进行调节。因此,尽管这些蛋白质占人类基因的30%左右,但它们包含了FDA批准的大多数药物靶点,这一点也不奇怪。即便如此,大多数分泌蛋白和膜蛋白在结合伴侣和细胞功能方面仍未被表征。为了解决这个问题,已经开发了许多方法来克服与膜蛋白生物学和ePPI发现相关的挑战。本章将涵盖使用高通量方法的最新进展,以实现人类eppi综合网络的生成,以用于未来的靶向药物发现。
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Unbiased Identification of Extracellular Protein–Protein Interactions for Drug Target and Biologic Drug Discovery
Technological improvements in unbiased screening have accelerated drug target discovery. In particular, membrane-embedded and secreted proteins have gained attention because of their ability to orchestrate intercellular communication. Dysregulation of their extracellular protein–protein interactions (ePPIs) underlies the initiation and progression of many human diseases. Practically, ePPIs are also accessible for modulation by therapeutics since they operate outside of the plasma membrane. Therefore, it is unsurprising that while these proteins make up about 30% of human genes, they encompass the majority of drug targets approved by the FDA. Even so, most secreted and membrane proteins remain uncharacterized in terms of binding partners and cellular functions. To address this, a number of approaches have been developed to overcome challenges associated with membrane protein biology and ePPI discovery. This chapter will cover recent advances that use high-throughput methods to move towards the generation of a comprehensive network of ePPIs in humans for future targeted drug discovery.
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Targeting the Aryl Hydrocarbon Receptor (AhR): A Review of the In-Silico Screening Approaches to Identify AhR Modulators Design and Implementation of High Throughput Screening Assays for Drug Discoveries Unbiased Identification of Extracellular Protein–Protein Interactions for Drug Target and Biologic Drug Discovery
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