Unknown

Dataset Information

0

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


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.

SUBMITTER: Yuan Y 

PROVIDER: S-EPMC5426343 | biostudies-literature | 2017 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

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

Yuan Youyong Y   Zhang Chong-Jing CJ   Kwok Ryan T K RTK   Mao Duo D   Tang Ben Zhong BZ   Liu Bin B   Liu Bin B  

Chemical science 20170109 4


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-fluor  ...[more]

Similar Datasets

| S-EPMC6013802 | biostudies-other
| S-EPMC3462246 | biostudies-literature
| S-EPMC7497988 | biostudies-literature
| S-EPMC5771094 | biostudies-literature
| S-EPMC5501095 | biostudies-literature
| S-EPMC6731743 | biostudies-literature
| S-EPMC3895904 | biostudies-literature
| S-EPMC8319955 | biostudies-literature
| S-EPMC5840378 | biostudies-literature
| S-EPMC7307831 | biostudies-literature