Department of Neuroscience, Mount Sinai School of Medicine , New York, New York 10029, United States.
Department of Physiology, Feinberg School of Medicine, Northwestern University , Chicago, Illinois 60611, United States.
ACS Chem Neurosci. 2017 Oct 18;8(10):2139-2144. doi: 10.1021/acschemneuro.7b00237. Epub 2017 Aug 1.
We have made a new caged cGMP that is photolyzed with blue light. Using our recently developed derivative of 7-diethylaminocourmarin (DEAC) called DEAC450, we synthesized coumarin phosphoester derivatives of cGMP with two negative charges appended to the DEAC450 moiety. DEAC450-cGMP is freely soluble in physiological buffer without the need for any organic cosolvents. With a photolysis quantum yield of 0.18 and an extinction coefficient of 43 000 M cm at 453 nm, DEAC450-cGMP is the most photosensitive caged cGMP made to date. In patch-clamped neurons in acutely isolated brain slices, blue light effectively uncaged cGMP from DEAC450 and facilitated activation of hyperpolarization and cyclic nucleotide gated cation (HCN) channels in cholinergic interneurons. Thus, DEAC450-cGMP has a unique set of optical and chemical properties that make it a useful addition to the optical arsenal available to neurobiologists.
我们合成了一种新的笼状 cGMP,它可以用蓝光进行光解。我们使用最近开发的 7-二乙氨基香豆素(DEAC)衍生物 DEAC450,将 cGMP 的磷酸酯衍生物与两个负电荷附加到 DEAC450 部分上。DEAC450-cGMP 在生理缓冲液中自由溶解,无需任何有机溶剂。DEAC450-cGMP 的光解量子产率为 0.18,在 453nm 处的消光系数为 43000M cm,是迄今为止制造的最敏感的笼状 cGMP。在急性分离脑片的 patched 神经元中,蓝光有效地从 DEAC450 中释放 cGMP,并促进胆碱能中间神经元的超极化和环核苷酸门控阳离子(HCN)通道的激活。因此,DEAC450-cGMP 具有独特的光学和化学性质,使其成为神经生物学家可用的光学武器库中的有用补充。