Perelman School of Medicine, Department of Anesthesiology and Critical Care, University of Pennsylvania, John Morgan Building, 3620 Hamilton Walk, Philadelphia, Pennsylvania 19104, United States.
Perelman School of Medicine, Department of Biochemistry and Biophysics, Smilow Center for Translational Research, University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, Pennsylvania 19104, United States.
ACS Chem Neurosci. 2021 Jan 6;12(1):176-183. doi: 10.1021/acschemneuro.0c00667. Epub 2020 Dec 23.
The mechanisms of general anesthetics have been debated in the literature for many years and continue to be of great interest. As anesthetic molecules are notoriously difficult to study due to their low binding affinities and multitude of binding partners, it is advantageous to have additional tools to study these interactions. Fropofol is a hydroxyl to fluorine-substituted propofol analogue that is able to antagonize the actions of propofol. Understanding fropofol's ability to antagonize propofol would facilitate further characterization of the binding interactions of propofol that may contribute to its anesthetic actions. However, the study of fropofol's molecular interactions has many of the same difficulties as its parent compound. Here, we present the synthesis and characterization of -azi-fropofol (AziF) as a suitable photoaffinity label (PAL) of fropofol that can be used to covalently label proteins of interest to characterize fropofol's binding interactions and their contribution to general anesthetic antagonism.
全麻机制在文献中已经争论了很多年,并且仍然是人们非常感兴趣的话题。由于麻醉分子的结合亲和力低,结合伴侣众多,因此很难研究,因此有额外的工具来研究这些相互作用是有利的。氟丙酚是一种羟基到氟取代的丙泊酚类似物,能够拮抗丙泊酚的作用。了解氟丙酚拮抗丙泊酚的能力将有助于进一步表征丙泊酚的结合相互作用,这可能有助于其麻醉作用。然而,氟丙酚的分子相互作用的研究与母体化合物有许多相同的困难。在这里,我们提出了 -azi-fropofol(AziF)的合成和表征,作为氟丙酚的合适光亲和标记物(PAL),可用于共价标记感兴趣的蛋白质,以表征氟丙酚的结合相互作用及其对全身麻醉拮抗作用的贡献。