Literature DB >> 31846307

Bioorthogonal "Labeling after Recognition" Affording an FRET-Based Luminescent Probe for Detecting and Imaging Caspase-3 via Photoluminescence Lifetime Imaging.

Qi Wu1, Kenneth Yin Zhang1, Peiling Dai1, Hengyu Zhu1, Yun Wang1, Linna Song1, Ling Wang1, Shujuan Liu1, Qiang Zhao1, Wei Huang1,2.   

Abstract

Bis-labeling with a luminescent energy donor/acceptor pair onto biological substrates affords probes which give FRET readouts for the detection of interaction partners. However, the covalently bound luminophores bring about steric hindrance and nonspecific interaction, which probably perturb the biological recognition. Herein, we designed a highly sensitive and specific "labeling after recognition" sensing approach, where luminophore labeling occurred after the biological recognition. Taking the cutting enzyme caspase-3 as an example, we demonstrated the detection of its catalytic activity in solution and apoptotic cells using the tetrapeptide motif Asp-Glu-Val-Asp (DEVD) as the cleavable substrate, and an iridium(III) complex and a rhodamine derivative as the energy donor/acceptor pair. The DEVD tetrapeptide was modified with an azide and a GK-norbornylene groups at the amino and carboxyl terminuses, respectively, which allowed donor/acceptor bis-labeling via two independent catalysis-free bioorthogonal reactions. The phosphorescence lifetime of the iridium(III) complex was quenched upon bis-labeling owing to the intracellular FRET to the rhodamine derivative, and significantly elongated upon the peptide being catalytically cleaved by caspase-3. Interestingly, the sensitivity and efficiency of the lifetime responses were much higher in the "labeling after recognition" sensing approach. Molecular docking analysis showed that the steric hindrance and nonspecific interactions partially inhibited the biological recognition of the DEVD substrate by caspase-3. The imaging of the catalytic activity of caspase-3 in apoptotic cells was demonstrated via photoluminescence lifetime imaging microscopy. Lifetime analysis not only confirmed the occurrence of intracellular bioorthogonal bis-labeling and catalytic cleavage, but also showed the extent to which the two dynamic processes occurred.

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Year:  2019        PMID: 31846307     DOI: 10.1021/jacs.9b12191

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  6 in total

Review 1.  Phosphorescent Ir(III) Complexes for Biolabeling and Biosensing.

Authors:  Byung Hak Jhun; Dayoon Song; Soo Young Park; Youngmin You
Journal:  Top Curr Chem (Cham)       Date:  2022-08-10

2.  A Coumarin-Porphyrin FRET Break-Apart Probe for Heme Oxygenase-1.

Authors:  Edward R H Walter; Ying Ge; Justin C Mason; Joseph J Boyle; Nicholas J Long
Journal:  J Am Chem Soc       Date:  2021-04-12       Impact factor: 15.419

3.  Completely aqueous processable stimulus responsive organic room temperature phosphorescence materials with tunable afterglow color.

Authors:  Dan Li; Yujie Yang; Jie Yang; Manman Fang; Ben Zhong Tang; Zhen Li
Journal:  Nat Commun       Date:  2022-01-17       Impact factor: 14.919

Review 4.  Activated molecular probes for enzyme recognition and detection.

Authors:  Meng Yuan; Ying Wu; Caiyan Zhao; Zhongxiang Chen; Lichao Su; Huanghao Yang; Jibin Song
Journal:  Theranostics       Date:  2022-01-01       Impact factor: 11.556

5.  Stimulus-responsive room temperature phosphorescence materials with full-color tunability from pure organic amorphous polymers.

Authors:  Dan Li; Jie Yang; Manman Fang; Ben Zhong Tang; Zhen Li
Journal:  Sci Adv       Date:  2022-02-25       Impact factor: 14.136

6.  Real-time tracking of ER turnover during ERLAD by a rhenium complex via lifetime imaging.

Authors:  Liang Hao; Yu-Yi Ling; Zhi-Xin Huang; Zheng-Yin Pan; Cai-Ping Tan; Zong-Wan Mao
Journal:  Natl Sci Rev       Date:  2021-10-28       Impact factor: 23.178

  6 in total

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