Butts Christopher A, Xi Jin, Brannigan Grace, Saad Abdalla A, Venkatachalan Srinivasan P, Pearce Robert A, Klein Michael L, Eckenhoff Roderic G, Dmochowski Ivan J
Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A. 2009 Apr 21;106(16):6501-6. doi: 10.1073/pnas.0810590106. Epub 2009 Apr 3.
We identified a fluorophore, 1-aminoanthracene (1-AMA), that is anesthetic, potentiates GABAergic transmission, and gives an appropriate dissociation constant, K(d) approximately 0.1 mM, for binding to the general anesthetic site in horse spleen apoferritin (HSAF). 1-AMA fluorescence is enhanced when bound to HSAF. Thus, displacement of 1-AMA from HSAF by other anesthetics attenuates the fluorescence signal and allows determination of K(d), as validated by isothermal titration calorimetry. This provides a unique fluorescence assay for compound screening and anesthetic discovery. Additional electrophysiology experiments in isolated cells indicate that 1-AMA potentiates chloride currents elicited by GABA, similar to many general anesthetics. Furthermore, 1-AMA reversibly immobilizes stage 45-50 Xenopus laevis tadpoles (EC(50) = 16 microM) and fluorescence micrographs show 1-AMA localized to brain and olfactory regions. Thus, 1-AMA provides an unprecedented opportunity for studying general anesthetic distribution in vivo at the cellular and subcellular levels.
我们鉴定出一种荧光团,即1-氨基蒽(1-AMA),它具有麻醉作用,能增强GABA能传递,并且对于与马脾脱铁铁蛋白(HSAF)中的全身麻醉位点结合具有合适的解离常数K(d),约为0.1 mM。当与HSAF结合时,1-AMA的荧光会增强。因此,其他麻醉剂将1-AMA从HSAF上置换下来会减弱荧光信号,并能测定K(d),等温滴定量热法已验证了这一点。这为化合物筛选和麻醉剂发现提供了一种独特的荧光检测方法。在分离细胞中进行的额外电生理实验表明,1-AMA增强了由GABA引发的氯离子电流,这与许多全身麻醉剂类似。此外,1-AMA能使处于45 - 50期的非洲爪蟾蝌蚪可逆性固定(半数有效浓度EC(50) = 16 microM),荧光显微照片显示1-AMA定位于大脑和嗅觉区域。因此,1-AMA为在细胞和亚细胞水平研究体内全身麻醉剂的分布提供了前所未有的机会。