Department of Neurochemistry, Institute of Physiology CAS, 142 20 Prague, Czech Republic.
Department of Experimental and Clinical Pharmacology, University of Minnesota College of Pharmacy, Minneapolis, MN 55455, USA.
Biomolecules. 2020 Feb 18;10(2):325. doi: 10.3390/biom10020325.
Allosteric modulators are ligands that bind to a site on the receptor that is spatially separated from the orthosteric binding site for the endogenous neurotransmitter. Allosteric modulators modulate the binding affinity, potency, and efficacy of orthosteric ligands. Muscarinic acetylcholine receptors are prototypical allosterically-modulated G-protein-coupled receptors. They are a potential therapeutic target for the treatment of psychiatric, neurologic, and internal diseases like schizophrenia, Alzheimer's disease, Huntington disease, type 2 diabetes, or chronic pulmonary obstruction. Here, we reviewed the progress made during the last decade in our understanding of their mechanisms of binding, allosteric modulation, and in vivo actions in order to understand the translational impact of studying this important class of pharmacological agents. We overviewed newly developed allosteric modulators of muscarinic receptors as well as new spin-off ideas like bitopic ligands combining allosteric and orthosteric moieties and photo-switchable ligands based on bitopic agents.
变构调节剂是一类配体,它们结合到受体上与内源性神经递质的正位结合位点在空间上分开的位点。变构调节剂调节正位配体的结合亲和力、效力和效能。毒蕈碱型乙酰胆碱受体是典型的变构调节 G 蛋白偶联受体。它们是治疗精神疾病、神经疾病和内部疾病(如精神分裂症、阿尔茨海默病、亨廷顿病、2 型糖尿病或慢性阻塞性肺病)的潜在治疗靶点。在这里,我们回顾了过去十年中在理解它们的结合机制、变构调节以及体内作用方面所取得的进展,以便了解研究这一类重要的药理学药物的转化影响。我们综述了毒蕈碱受体的新型变构调节剂,以及新的衍生想法,如结合变构和正位部分的双位点配体,以及基于双位点配体的光可切换配体。