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基于 BODIPY 的实时、可逆和靶向生物硫醇荧光探针用于活细胞中的生物硫醇成像。

BODIPY based realtime, reversible and targeted fluorescent probes for biothiol imaging in living cells.

机构信息

Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.

出版信息

Chem Commun (Camb). 2020 Dec 4;56(93):14717-14720. doi: 10.1039/d0cc06313d. Epub 2020 Nov 11.

Abstract

Real-time live cell imaging and quantification of biothiol dynamics are important for understanding pathophysiological processes. However, the design and synthesis of rational probes that have reversible and real-time capabilities is still challenging. In this work, we have prepared boron-dipyrrolemethene (BODIPY) based fluorescent molecules as ratiometric probes that allow the real-time biothiol dynamics to be observed in living cells. The Michael reaction between α-formyl-BODIPY (BOD-JQ) and GSH exhibited a reversible fluorogenic mechanism with fluorescent emission shifting from 592 nm to 544 nm with t = 16 ms. In particular, we showed that the probes with targeting agents are capable of detecting biothiols in mitochondria and the endoplasmic reticulum (ER) with high temporal resolution.

摘要

实时活细胞成像和生物硫醇动力学的定量分析对于理解病理生理过程非常重要。然而,设计和合成具有可逆性和实时性的合理探针仍然具有挑战性。在这项工作中,我们制备了基于硼二吡咯甲川(BODIPY)的荧光分子作为比率探针,可实时观察活细胞中的生物硫醇动力学。α-甲酰基-BODIPY(BOD-JQ)与 GSH 之间的迈克尔反应表现出可逆的荧光发生机制,荧光发射从 592nm 转移到 544nm,t = 16ms。特别地,我们表明,带有靶向剂的探针能够以高时间分辨率检测线粒体和内质网(ER)中的生物硫醇。

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