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Photoactivatable drugs for nicotinic optopharmacology
Nature Methods ( IF 36.1 ) Pub Date : 2018-03-26 , DOI: 10.1038/nmeth.4637
Sambashiva Banala 1 , Matthew C Arvin 2 , Nicholas M Bannon 3 , Xiao-Tao Jin 2 , John J Macklin 1 , Yong Wang 2 , Can Peng 2 , Guiqing Zhao 2 , John J Marshall 4 , Kyle R Gee 5 , David L Wokosin 4 , Veronica J Kim 2 , J Michael McIntosh 6 , Anis Contractor 3, 4 , Henry A Lester 1, 7 , Yevgenia Kozorovitskiy 3 , Ryan M Drenan 2 , Luke D Lavis 1
Affiliation  

Photoactivatable pharmacological agents have revolutionized neuroscience, but the palette of available compounds is limited. We describe a general method for caging tertiary amines by using a stable quaternary ammonium linkage that elicits a red shift in the activation wavelength. We prepared a photoactivatable nicotine (PA-Nic), uncageable via one- or two-photon excitation, that is useful to study nicotinic acetylcholine receptors (nAChRs) in different experimental preparations and spatiotemporal scales.



中文翻译:

用于烟碱光药理学的光激活药物

光活化药物已经彻底改变了神经科学,但可用化合物的范围有限。我们描述了一种通过使用稳定的季铵键来封闭叔胺的通用方法,该键会引起激活波长的红移。我们制备了一种光活化尼古丁(PA-Nic),通过一个或两个光子激发无法控制,这对于在不同的实验准备和时空尺度上研究烟碱乙酰胆碱受体(nAChR)很有用。

更新日期:2018-03-26
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