Carbon dots-based red fluorescence nanoprobe for caspase-1 activity assay and living cell imaging

A novel fluorescent “turn on” nanoprobe for caspase-1 activity assay has been constructed based on conjugation of AuNRs and RCDs through a short peptide. This fabrication and detection strategy provides high sensitivity, specificity, and stability in cell extract sample detection and in-situ living...

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Veröffentlicht in:Sensors and actuators. B, Chemical Chemical, 2021-10, Vol.344, p.130285, Article 130285
Hauptverfasser: Wang, Gai-Gai, Lv, Qi-Yan, Song, Xiaojie, Cui, Hui-Fang
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Lv, Qi-Yan
Song, Xiaojie
Cui, Hui-Fang
description A novel fluorescent “turn on” nanoprobe for caspase-1 activity assay has been constructed based on conjugation of AuNRs and RCDs through a short peptide. This fabrication and detection strategy provides high sensitivity, specificity, and stability in cell extract sample detection and in-situ living cell imaging. [Display omitted] •A novel fluorescence nanoprobe were constructed for caspase-1 activity analysis.•The facet-controlled AuNRs improve fluorescence surface energy transfer efficiency.•Prior treated the AuNRs with PEG-SH enhanced the stability of the nanoprobe.•The nanoprobe determine caspase-1 activity sensitively with a LOD of 1.76 ng mL-1.•The fluorescence nanoprobe can probe the intracellular caspase-1 activity levels. The development of sensitive and convenient strategies for monitoring intracellular caspase-1 activity is of great significance. Herein, a novel fluorescence nanoprobe for caspase-1 activity determination was constructed based on surface energy transfer (SET) between red-emissive carbon dots (RCDs) as a donor, and Au nanorods (AuNRs) as an acceptor. The donor/acceptor pair were covalently bridged with a peptide containing a caspase-1 cleavage site (YVAD) at middle. The stability and dispersivity of the AuNR-Pep-RCD nanoprobe was realized/enhanced by pretreating the AuNRs with PEG-SH. Active caspase-1 cleaves the YVAD site, releasing RCDs and recovering the fluorescence. Synergic effect of the red-emission, sensitive and selective cleavage, and excellent SET efficiency contribute to the nanoprobe with high sensitivity and selectivity, especially in biological samples. More importantly, the nanoprobe can be uptaken by living cells, capable of in-situ intracellular caspase-1 activity imaging. The fluorescence recovery is linearly correlated with caspase-1 activity in the range of 5‒300 ng·mL−1 (2.5 × 10−5‒1.3 × 10−3 U·mL−1), with a limit of detection of 1.76 ng·mL−1 (8.8 × 10-6 U·mL−1). In particular, the fluorescence nanoprobe can accurately detect caspase-1 activity in cells extract, and sensitively probe the caspase-1 activation treatment and inhibition treatment for the intracellular caspase-1 activity levels.
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This fabrication and detection strategy provides high sensitivity, specificity, and stability in cell extract sample detection and in-situ living cell imaging. [Display omitted] •A novel fluorescence nanoprobe were constructed for caspase-1 activity analysis.•The facet-controlled AuNRs improve fluorescence surface energy transfer efficiency.•Prior treated the AuNRs with PEG-SH enhanced the stability of the nanoprobe.•The nanoprobe determine caspase-1 activity sensitively with a LOD of 1.76 ng mL-1.•The fluorescence nanoprobe can probe the intracellular caspase-1 activity levels. The development of sensitive and convenient strategies for monitoring intracellular caspase-1 activity is of great significance. Herein, a novel fluorescence nanoprobe for caspase-1 activity determination was constructed based on surface energy transfer (SET) between red-emissive carbon dots (RCDs) as a donor, and Au nanorods (AuNRs) as an acceptor. The donor/acceptor pair were covalently bridged with a peptide containing a caspase-1 cleavage site (YVAD) at middle. The stability and dispersivity of the AuNR-Pep-RCD nanoprobe was realized/enhanced by pretreating the AuNRs with PEG-SH. Active caspase-1 cleaves the YVAD site, releasing RCDs and recovering the fluorescence. Synergic effect of the red-emission, sensitive and selective cleavage, and excellent SET efficiency contribute to the nanoprobe with high sensitivity and selectivity, especially in biological samples. More importantly, the nanoprobe can be uptaken by living cells, capable of in-situ intracellular caspase-1 activity imaging. The fluorescence recovery is linearly correlated with caspase-1 activity in the range of 5‒300 ng·mL−1 (2.5 × 10−5‒1.3 × 10−3 U·mL−1), with a limit of detection of 1.76 ng·mL−1 (8.8 × 10-6 U·mL−1). 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B, Chemical</title><description>A novel fluorescent “turn on” nanoprobe for caspase-1 activity assay has been constructed based on conjugation of AuNRs and RCDs through a short peptide. This fabrication and detection strategy provides high sensitivity, specificity, and stability in cell extract sample detection and in-situ living cell imaging. [Display omitted] •A novel fluorescence nanoprobe were constructed for caspase-1 activity analysis.•The facet-controlled AuNRs improve fluorescence surface energy transfer efficiency.•Prior treated the AuNRs with PEG-SH enhanced the stability of the nanoprobe.•The nanoprobe determine caspase-1 activity sensitively with a LOD of 1.76 ng mL-1.•The fluorescence nanoprobe can probe the intracellular caspase-1 activity levels. The development of sensitive and convenient strategies for monitoring intracellular caspase-1 activity is of great significance. Herein, a novel fluorescence nanoprobe for caspase-1 activity determination was constructed based on surface energy transfer (SET) between red-emissive carbon dots (RCDs) as a donor, and Au nanorods (AuNRs) as an acceptor. The donor/acceptor pair were covalently bridged with a peptide containing a caspase-1 cleavage site (YVAD) at middle. The stability and dispersivity of the AuNR-Pep-RCD nanoprobe was realized/enhanced by pretreating the AuNRs with PEG-SH. Active caspase-1 cleaves the YVAD site, releasing RCDs and recovering the fluorescence. Synergic effect of the red-emission, sensitive and selective cleavage, and excellent SET efficiency contribute to the nanoprobe with high sensitivity and selectivity, especially in biological samples. More importantly, the nanoprobe can be uptaken by living cells, capable of in-situ intracellular caspase-1 activity imaging. 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[Display omitted] •A novel fluorescence nanoprobe were constructed for caspase-1 activity analysis.•The facet-controlled AuNRs improve fluorescence surface energy transfer efficiency.•Prior treated the AuNRs with PEG-SH enhanced the stability of the nanoprobe.•The nanoprobe determine caspase-1 activity sensitively with a LOD of 1.76 ng mL-1.•The fluorescence nanoprobe can probe the intracellular caspase-1 activity levels. The development of sensitive and convenient strategies for monitoring intracellular caspase-1 activity is of great significance. Herein, a novel fluorescence nanoprobe for caspase-1 activity determination was constructed based on surface energy transfer (SET) between red-emissive carbon dots (RCDs) as a donor, and Au nanorods (AuNRs) as an acceptor. The donor/acceptor pair were covalently bridged with a peptide containing a caspase-1 cleavage site (YVAD) at middle. 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subjects Biological properties
Carbon dots
Caspase-1 activity
Cells (biology)
Cleavage
Energy transfer
Fluorescence
Fluorescence nanoprobe
Gold
Living cell imaging
Nanorods
Red emission
Selectivity
Surface energy
Surface energy transfer
title Carbon dots-based red fluorescence nanoprobe for caspase-1 activity assay and living cell imaging
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