Sakamoto Seiji, Yamaura Kei, Numata Tomohiro, Harada Fumio, Amaike Kazuma, Inoue Ryuji, Kiyonaka Shigeki, Hamachi Itaru
Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.
Department of Physiology, School of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.
ACS Cent Sci. 2019 Sep 25;5(9):1541-1553. doi: 10.1021/acscentsci.9b00539. Epub 2019 Aug 16.
γ-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the central nervous system. The fast inhibitory actions of GABA are mainly mediated by GABA receptors (GABARs), which are widely recognized as clinically relevant drug targets. However, it remains difficult to create screening systems for drug candidates that act on GABARs because of the existence of multiple ligand-binding sites and the delicate pentameric structures of GABARs. We here developed the first turn-on fluorescent imaging probe for GABARs, which can be used to quantitatively evaluate ligand-receptor interactions under live cell conditions. Using noncovalent labeling of GABARs with this turn-on probe, a new imaging-based ligand assay system, which allows discovery of positive allosteric modulators (PAMs) for the GABAR, was successfully constructed. Our system is applicable to high-throughput ligand screening, and we discovered new small molecules that function as PAMs for GABARs. These results highlight the power of the use of a turn-on fluorescent probe to screen drugs for complicated membrane proteins that cannot be addressed by conventional methods.
γ-氨基丁酸(GABA)是中枢神经系统中的主要抑制性神经递质。GABA的快速抑制作用主要由GABA受体(GABARs)介导,GABARs被广泛认为是临床相关的药物靶点。然而,由于GABARs存在多个配体结合位点以及精细的五聚体结构,为作用于GABARs的候选药物创建筛选系统仍然很困难。我们在此开发了首个用于GABARs的开启式荧光成像探针,可用于在活细胞条件下定量评估配体-受体相互作用。通过使用这种开启式探针非共价标记GABARs,成功构建了一种基于成像的新型配体检测系统,该系统能够发现GABAR的正变构调节剂(PAMs)。我们的系统适用于高通量配体筛选,并且我们发现了可作为GABARs的PAMs的新小分子。这些结果凸显了使用开启式荧光探针筛选传统方法无法解决的复杂膜蛋白药物的强大作用。