| Literature DB >> 33744680 |
Wenting Cheng1, Jiehua Ma2, Liangliang Xiang3, Ying Sun1, Wei Huang1, Zhaoli Zhang3, Dehua Kong4, Jinlong Li5.
Abstract
An electrochemical platform has been developed to detect protein kinase activity through the combined actions of Zr4+ mediated signal transition and hybridization chain reaction (HCR)-stimulated DNAzymes nanowires. First of all, protein kinase A (PKA) phosphorylates substrate peptides immobilized on gold electrode surface. Thereafter, the DNA1 containing 5'-phosphoryl ends is linked to the phosphorylated substrate peptide via the robust phosphate-Zr4+-phosphate linkages. By the introduction of molecular beacons (MBs), the DNA1 can open the hairpin structures of MBs through toehold mediated strand displacement (TMSDR), leading to an autonomous stem-opening process and subsequent assembly of G-quadruplex-containing DNA chains by HCR. After the addition of hemin, the formed HRP-mimicking DNAzymes can catalyze the hydroquinone-H2O2 system to generate amplified electrochemical signals. As expected, this method can achieve ultrahigh analytical performance with a low detection limit of 0.02U/mL and exhibit high cost-savings potential without the need for antibody, protease and labeling. Therefore, this method can serve as a new tool for the assay of protein kinase A and its inhibitor screening in the future.Entities:
Keywords: Electrochemical biosensor; HCR; PKA activity; Phosphorylation; Zr(4+)
Year: 2021 PMID: 33744680 DOI: 10.1016/j.bioelechem.2021.107796
Source DB: PubMed Journal: Bioelectrochemistry ISSN: 1567-5394 Impact factor: 5.373