Amundarain María Julia, Ribeiro Rui Pedro, Costabel Marcelo Daniel, Giorgetti Alejandro
Departamento de Física, Instituto de Física del Sur (IFISUR), Universidad Nacional del Sur (UNS), CONICET, Av L N Alem 1253, B8000CPB - Bahía Blanca, Argentina.
Department of Biotechnology, University of Verona, Strada Le Grazie 15, I-37134 Verona, Italy.
Future Med Chem. 2019 Feb;11(3):229-245. doi: 10.4155/fmc-2018-0336. Epub 2019 Feb 25.
The pentameric γ-aminobutyric acid type A receptors are ion channels activated by ligands, which intervene in the rapid inhibitory transmission in the mammalian CNS. Due to their rich pharmacology and therapeutic potential, it is essential to understand their structure and function thoroughly. This deep characterization was hampered by the lack of experimental structural information for many years. Thus, computational techniques have been extensively combined with experimental data, in order to undertake the study of γ-aminobutyric acid type A receptors and their interaction with drugs. Here, we review the exciting journey made to assess the structures of these receptors and outline major outcomes. Finally, we discuss the brand new structure of the αβγ subtype and the amazing advances it brings to the field.
五聚体A型γ-氨基丁酸受体是由配体激活的离子通道,其参与哺乳动物中枢神经系统中的快速抑制性传递。由于其丰富的药理学特性和治疗潜力,全面了解其结构和功能至关重要。多年来,由于缺乏实验结构信息,这一深入表征受到了阻碍。因此,计算技术已广泛与实验数据相结合,以开展对A型γ-氨基丁酸受体及其与药物相互作用的研究。在此,我们回顾了为评估这些受体结构所经历的激动人心的历程,并概述了主要成果。最后,我们讨论了αβγ亚型的全新结构及其给该领域带来的惊人进展。