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一种用于通过多重 FLIM-EPR 光谱法可视化和定量组织中靶分子的双荧光-自旋标记探针。

A Dual Fluorescence-Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM-EPR Spectroscopy.

机构信息

Department of Dermatology, Venereology and Allergology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.

Freie Universität Berlin, Institute of Pharmacy, Berlin, Germany.

出版信息

Angew Chem Int Ed Engl. 2021 Jun 25;60(27):14938-14944. doi: 10.1002/anie.202012852. Epub 2021 May 26.

Abstract

Simultaneous visualization and concentration quantification of molecules in biological tissue is an important though challenging goal. The advantages of fluorescence lifetime imaging microscopy (FLIM) for visualization, and electron paramagnetic resonance (EPR) spectroscopy for quantification are complementary. Their combination in a multiplexed approach promises a successful but ambitious strategy because of spin label-mediated fluorescence quenching. Here, we solved this problem and present the molecular design of a dual label (DL) compound comprising a highly fluorescent dye together with an EPR spin probe, which also renders the fluorescence lifetime to be concentration sensitive. The DL can easily be coupled to the biomolecule of choice, enabling in vivo and in vitro applications. This novel approach paves the way for elegant studies ranging from fundamental biological investigations to preclinical drug research, as shown in proof-of-principle penetration experiments in human skin ex vivo.

摘要

在生物组织中同时可视化和定量分子是一个重要但具有挑战性的目标。荧光寿命成像显微镜 (FLIM) 在可视化方面的优势,以及电子顺磁共振 (EPR) 光谱法在定量方面的优势是互补的。它们在多路复用方法中的结合有望成为一种成功但雄心勃勃的策略,因为这是基于自旋标记介导的荧光猝灭。在这里,我们解决了这个问题,并提出了一种双标记 (DL) 化合物的分子设计,该化合物由高荧光染料和 EPR 自旋探针组成,这也使荧光寿命对浓度敏感。DL 可以很容易地与所需的生物分子结合,从而能够进行体内和体外应用。这种新方法为从基础生物学研究到临床前药物研究的优雅研究铺平了道路,正如在人体皮肤 ex vivo 的原理验证渗透实验中所展示的那样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a444/8251738/e1bc0a86de31/ANIE-60-14938-g002.jpg

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