被劫持的受体

David J Triggle
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引用次数: 2

摘要

药理学受体通常由它们对配体识别的选择性来定义,包括在适当的情况下相互作用的立体选择性。越来越清楚的是,受体实际上可能是混杂的物种。这种乱交出现在几个层次的组织中:其中两个似乎特别重要。给定的配体-受体复合物可能与不同的效应器偶联,并可能产生完全不同的生理反应:对于G蛋白偶联受体来说,这是特别常见的,尽管不是唯一的。或者,单个受体可能识别本质上不同的配体,通常具有显著不同的特征:许多病毒通过与神经递质、肽或激素受体的相互作用进入细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hijacked receptors

Pharmacological receptors are typically defined by their selectivity of ligand recognition, including where appropriate stereoselectivity of interaction. It is increasingly clear that receptors may, in fact, be promiscuous species. This promiscuity arises at several levels of organization: two appear to be of particular importance. A given ligand–receptor complex may couple with different effectors and may generate quite different physiological responses: this is particularly common, although not uniquely so, for G protein-coupled receptors. Or a single receptor may recognize fundamentally different ligands often of significantly different characteristics: a number of viruses gain entry to cells through their interaction at receptors for neurotransmitters, peptides or hormones.

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