Issue 81, 2015

A ‘signal on-off’ electrochemical peptide biosensor for matrix metalloproteinase 2 based on target induced cleavage of a peptide

Abstract

In this work, a ‘signal on-off’ electrochemical peptide biosensor was developed for the determination of matrix metalloproteinase 2 (MMP-2) on the basis of target induced cleavage of a specific peptide. The prepared single-stranded DNA–porous platinum nanoparticles–peptide (S1–pPtNPs–P1) bioconjugates were employed as nanoprobes, where the specific peptide (P1, biotin–Gly–Pro–Leu–Gly–Val–Arg–Gly–Lys–Gly–Gly–Cys) was used as a cleavage-sensing element, offering the capability of ‘on-off’ electrochemical signalling for the target MMP-2. As for the construction of the biosensor, S1–pPtNPs–P1 was immobilized on the electrode surface through the conjunction of biotin–streptavidin. Then, hybridization chain reaction (HCR) was triggered to embed the electroactive thionine (Thi). The pPtNPs could effectively catalyze the decomposition of added H2O2, resulting in the electrochemical signal of Thi being enhanced significantly (‘signal on’ state). Upon sensing cleavage with MMP-2, pPtNPs and eletroactive Thi left the electrode surface, leading to an observable decrease in the electrochemical signal of Thi (‘signal off’ state). Compared with other methods of detecting MMP-2, the proposed ‘signal on-off’ electrochemical peptide biosensor exhibited an improved sensitivity with a detection limit of 0.32 pg mL−1 and wide linear range from 1 pg mL−1 to 10 ng mL−1.

Graphical abstract: A ‘signal on-off’ electrochemical peptide biosensor for matrix metalloproteinase 2 based on target induced cleavage of a peptide

Supplementary files

Article information

Article type
Paper
Submitted
05 Jun 2015
Accepted
25 Jul 2015
First published
27 Jul 2015

RSC Adv., 2015,5, 65725-65730

Author version available

A ‘signal on-off’ electrochemical peptide biosensor for matrix metalloproteinase 2 based on target induced cleavage of a peptide

P. Jing, H. Yi, S. Xue, R. Yuan and W. Xu, RSC Adv., 2015, 5, 65725 DOI: 10.1039/C5RA10662A

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