Department of Chemistry, Molecular Design and Synthesis, KU Leuven Campus Arenberg Celestijnenlaan 200F -, box 2404, 3001, Leuven, Belgium.
Department of Neurosciences, Experimental Neurology and Leuven Brain Institute (LBI), KU Leuven Campus Gasthuisberg O&N5 -, box 602 Herestraat 49, 3000, Leuven, Belgium.
Chemistry. 2021 Jun 16;27(34):8605-8641. doi: 10.1002/chem.202100296. Epub 2021 Jun 1.
Despite the fact that transmembrane proteins represent the main therapeutic targets for decades, complete and in-depth knowledge about their biochemical and pharmacological profiling is not fully available. In this regard, target-tailored small-molecule fluorescent ligands are a viable approach to fill in the missing pieces of the puzzle. Such tools, coupled with the ability of high-precision optical techniques to image with an unprecedented resolution at a single-molecule level, helped unraveling many of the conundrums related to plasma proteins' life-cycle and druggability. Herein, we review the recent progress made during the last two decades in fluorescent ligand design and potential applications in fluorescence microscopy of voltage-gated ion channels, ligand-gated ion channels and G-coupled protein receptors.
尽管跨膜蛋白作为主要的治疗靶点已经有几十年了,但我们对于它们生化和药理学特性的了解还并不全面。在这方面,针对靶点的小分子荧光配体是一种可行的方法,可以填补其中的空白。这些工具与高精度光学技术结合使用,可以以前所未有的单分子水平分辨率进行成像,有助于解决与血浆蛋白生命周期和可药性相关的许多难题。本文综述了过去二十年中在设计荧光配体方面取得的进展,以及在荧光显微镜技术中应用于电压门控离子通道、配体门控离子通道和 G 蛋白偶联受体的潜在应用。