Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales , Universidad de Buenos Aires , Ciudad Universitaria , Buenos Aires C1428EGA , Argentina.
UMYMFOR , CONICET-Universidad de Buenos Aires , Ciudad Universitaria , Buenos Aires C1428EGA , Argentina.
J Med Chem. 2019 Jun 13;62(11):5250-5260. doi: 10.1021/acs.jmedchem.8b01400. Epub 2018 Dec 31.
Neurosteroids (NS) are the main modulators of γ-aminobutyric acid type A receptors (GABARs), which are the ligand-gated channels target of the major inhibitory neurotransmitter in vertebrates. As a consequence of their ability to modify inhibitory functions in the brain, NS have high physiological and clinical relevance. Accumulated evidence has strongly suggested that NS binding sites were located in the GABAR transmembrane domain; however the specific localization of these sites has remained an enigma for decades. Fortunately, recent resolution of GABARs crystal structures, together with computational strategies applied to investigate the NS binding, has paved the way to rationalizing the molecular basis of NS modulation. This work reviews from a historical perspective the road followed for establishing the GABAR/NS binding mode, from their initial molecular modeling to the latest findings. Furthermore, a comparative analysis describing the NS binding is provided, plus a preliminary analysis of putative NS sites in other assemblies.
神经甾体(NS)是γ-氨基丁酸 A 型受体(GABAR)的主要调节剂,GABAR 是脊椎动物主要抑制性神经递质的配体门控通道靶标。由于其能够调节大脑中的抑制功能,NS 具有很高的生理和临床相关性。大量证据强烈表明,NS 结合位点位于 GABAR 跨膜域;然而,这些位点的具体定位几十年来一直是个谜。幸运的是,最近 GABAR 晶体结构的解析,以及应用于研究 NS 结合的计算策略,为合理化 NS 调节的分子基础铺平了道路。这项工作从历史角度回顾了确定 GABAR/NS 结合模式的途径,从最初的分子建模到最新的发现。此外,还提供了对 NS 结合的比较分析,并对其他组合中的假定 NS 位点进行了初步分析。