Hibert M F, Trumpp-Kallmeyer S, Hoflack J, Bruinvels A
Department of Receptor Chemistry and Molecular Modelling, Marion Merrell Dow Research Institute, Strasbourg, France.
Trends Pharmacol Sci. 1993 Jan;14(1):7-12. doi: 10.1016/0165-6147(93)90106-t.
On his canvas entitled 'La trahison des Images' ('The Perfidy of Images'), René Magritte painted a tobacco pipe in a very realistic manner and added the words: 'Ceci n'est pas une pipe' ('This is not a pipe'). In similar style, it is of prime importance to state that the first three-dimensional (3D) models of G protein-coupled receptors (GPCRs) that have been defined and displayed are definitely not GPCRs and never will be. However, they probably represent a very important breakthrough in our understanding of GPCR structure and function as well as being a source of novel working hypotheses that can be experimentally explored. Several generations of scientists have elaborated their research on the concept of hormone-receptor interaction without having access to any structural representation of this molecular complex. Thus, for many years receptors remained only indirectly characterized through their functions or their binding properties. As a consequence, a number of important issues are still to be addressed. How does a hormone bind and activate its receptor? How does an antagonist inactivate a receptor? What is a partial agonist? What are the molecular mechanisms of signal transduction and modulation? Obviously, answers to these questions are of prime importance for medicinal chemists in their attempts to rationalize drug design.
勒内·马格利特在他的画作《形象的背叛》中,以非常写实的方式画了一只烟斗,并加上文字:“这不是一只烟斗”。以类似的方式,至关重要的是要表明,已定义并展示的G蛋白偶联受体(GPCR)的首批三维(3D)模型绝对不是GPCR,而且永远也不会是。然而,它们可能代表了我们在理解GPCR结构与功能方面的一个非常重要的突破,同时也是可以通过实验探索的新工作假设的来源。几代科学家在没有获得这种分子复合物任何结构表征的情况下,围绕激素 - 受体相互作用的概念开展了他们的研究。因此,多年来,受体仅通过其功能或结合特性进行间接表征。结果,许多重要问题仍有待解决。激素如何结合并激活其受体?拮抗剂如何使受体失活?什么是部分激动剂?信号转导和调节的分子机制是什么?显然,这些问题的答案对于药物化学家试图使药物设计合理化来说至关重要。