Woll Kellie A, Dailey William P, Brannigan Grace, Eckenhoff Roderic G
From the Departments of *Anesthesiology and Critical Care and †Pharmacology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania; ‡Department of Chemistry, University of Pennsylvania School of Arts and Sciences, Philadelphia, Pennsylvania; and §Department of Physics, Rutgers University, Camden, New Jersey.
Anesth Analg. 2016 Nov;123(5):1253-1262. doi: 10.1213/ANE.0000000000001365.
Anesthetic photoaffinity ligands have had an increasing presence within anesthesiology research. These ligands mimic parent general anesthetics and allow investigators to study anesthetic interactions with receptors and enzymes; identify novel targets; and determine distribution within biological systems. To date, nearly all general anesthetics used in medicine have a corresponding photoaffinity ligand represented in the literature. In this review, we examine all aspects of the current methodologies, including ligand design, characterization, and deployment. Finally we offer points of consideration and highlight the future outlook as more photoaffinity ligands emerge within the field.
麻醉光亲和配体在麻醉学研究中的应用日益广泛。这些配体模拟母体全身麻醉药,使研究人员能够研究麻醉药与受体和酶的相互作用;识别新的靶点;并确定其在生物系统中的分布。迄今为止,医学中使用的几乎所有全身麻醉药在文献中都有相应的光亲和配体。在本综述中,我们研究了当前方法的各个方面,包括配体设计、表征和应用。最后,我们提出了一些需要考虑的要点,并强调了随着该领域出现更多光亲和配体的未来前景。