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基于聚集诱导发光(AIE)gens的点亮型探针:用于半胱天冬酶级联激活监测的双信号开启

Light-up probe based on AIEgens: dual signal turn-on for caspase cascade activation monitoring.

作者信息

Yuan Youyong, Zhang Chong-Jing, Kwok Ryan T K, Mao Duo, Tang Ben Zhong, Liu Bin

机构信息

Department of Chemical and Biomolecular Engineering , National University of Singapore , 4 Engineering Drive 4 , Singapore 117585 . Email:

Department of Chemistry , The Hong Kong University of Science and Technology , Clear Water Bay , Kowloon , Hong Kong , China.

出版信息

Chem Sci. 2017 Apr 1;8(4):2723-2728. doi: 10.1039/c6sc04322d. Epub 2017 Jan 9.

Abstract

Direct monitoring of multiple enzyme activities in a given biological process is extremely important for disease diagnosis. Herein, we report a single fluorescent probe that targets two caspase activities in living cells. The probe consists of three parts that includes two AIE fluorogens with distinctive green and red emission colors excitable at a single wavelength, and a hydrophilic peptide as the substrate of the apoptosis initiator caspase-8 and the effector caspase-3. The probe is non-fluorescent in aqueous media. The green and red fluorescence can be sequentially turned on when the peptide substrate is cleaved by the cascade activation of caspase-8 and caspase-3 in early apoptotic HeLa cells induced by hydrogen peroxide. This sequential fluorescence turn-on allows real-time monitoring of the caspase cascade activation during the apoptotic process, which was further explored for evaluating the therapeutic efficiency of anticancer drugs. The probe design strategy developed in this study also proved to be general, which opens a new avenue for real-time, multiplexed imaging of cellular enzyme activity in a biological process.

摘要

在给定的生物过程中直接监测多种酶活性对于疾病诊断极为重要。在此,我们报告了一种针对活细胞中两种半胱天冬酶活性的单一荧光探针。该探针由三部分组成,包括两种具有独特绿色和红色发射颜色且可在单一波长激发的聚集诱导发光荧光团,以及一种亲水性肽,作为凋亡起始半胱天冬酶 -8 和效应半胱天冬酶 -3 的底物。该探针在水性介质中无荧光。当肽底物在过氧化氢诱导的早期凋亡HeLa细胞中通过半胱天冬酶 -8 和半胱天冬酶 -3 的级联激活被切割时,绿色和红色荧光可依次开启。这种顺序荧光开启允许在凋亡过程中实时监测半胱天冬酶级联激活,这进一步用于评估抗癌药物的治疗效果。本研究中开发的探针设计策略也被证明具有通用性,为生物过程中细胞酶活性的实时、多重成像开辟了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe28/5426343/4b4c61504b9c/c6sc04322d-s1.jpg

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