Allosteric Modulation of G Protein-Coupled Receptors: An Emerging Approach of Drug Discovery.

Austin journal of pharmacology and therapeutics Pub Date : 2014-01-01 Epub Date: 2014-02-27
Christopher Wild, Kathryn A Cunningham, Jia Zhou
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Abstract

Allosteric modulation of G protein-coupled receptors (GPCRs) confers several significant advantages over the traditional targeting of orthosteric sites. While the field of allosteric modulation of GPCRs as we now know it will benefit from continued investigation, the explosion of interest has led to a more in-depth understanding as to precisely how allosteric modulators may usher in a new paradigm for drug discovery.

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G蛋白偶联受体的变构调节:一种新兴的药物发现方法。
G蛋白偶联受体(gpcr)的变构调节与传统的正构位点靶向相比具有几个显著的优势。虽然我们现在知道gpcr的变构调节领域将受益于持续的研究,但兴趣的爆炸式增长已经导致了对变构调节剂如何引领药物发现新范式的更深入理解。
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