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Phosphopeptide-bridged NH-TiO-mediated carbon dots self-enhancing and electrochemiluminescence microsensors for label-free protein kinase A detection. | LitMetric

Phosphopeptide-bridged NH-TiO-mediated carbon dots self-enhancing and electrochemiluminescence microsensors for label-free protein kinase A detection.

Mikrochim Acta

State Key Laboratory of Food Nutrition and Safety, Tianjin Economy and Technology Development Area, Tianjin University of Science & Technology, 29 The Thirteenth Road, Tianjin, 300457, P.R. China.

Published: September 2024

A novel electrochemiluminescence (ECL) method was developed for determination of protein kinase A (PKA) ultra-sensitively based on amidated nano-titanium (NH-TiO) embellished carbon dots (Mg@N-CDs) fluorescent probe, which integrated the target recognition and ECL signal enhancement. The Cys-labeled kemptides were employed to build a serine-rich synthetic substrate-heptapeptide (Cys-kemptide) on the Au-electrode surface. Then, the PKA-induced biosensor was triggered as a signal switch to introduce the large amounts of TiO decorated Mg@N-CD nanohybrid (Ti@NMg-CDs) into AuE/Cys-phosphopeptides for signal output. In particular, the presence of PKA could induce the formation of Cys-phosphopeptides by the catalytic reaction between specific substrate (kemptide) and PKA, which acts as an initiator to link the Ti@NMg-CDs according to the bridge interactions Ti-O-P. In this way, multiple Cys-phosphopeptides were adsorbed onto a single Ti@NMg-CDs, and the Ti@NMg-CDs not only provided high specific selectivity but also large surface area, as well as unprecedented high ECL efficiency. Using this PKA-induced enhanced sensor, the limit of detection of the PKA was 4.89 × 10 U/mL (S/N = 3). The proposed ECL biosensor was also universally applicable for the screening of PKA inhibitors and determining of other kinases activity. Our sensing system has excellent performance of specificity and the screening of kinase inhibitors, as well as it will inspire future effort in clinical diagnostics and new drug discovery.

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Source
http://dx.doi.org/10.1007/s00604-024-06711-8DOI Listing

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