Peptide cleavage induced assembly enables highly sensitive electrochemiluminescence detection of protease activity

被引:18
作者
Cheng, Meng
Zhou, Jun
Zhou, Xiaoming [1 ]
Xing, Da
机构
[1] South China Normal Univ, Coll Biophoton, MOE Key Lab Laser Life Sci, Guangzhou 510631, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemiluminescence; Ru(bpy)(3)(2+)-2-cyanobenzothiazole; (Ru(bpy)(3)(2+)-(CBT); Peptide cleavage induced assembly; Trypsase; Caspase-3; BIOCOMPATIBLE CONDENSATION REACTION; GOLD NANOPARTICLES; TRYPSIN; ASSAY; BIOSENSOR; AMPLIFICATION; FLUORESCENCE; BIOMARKERS; ELECTRODE; SENSOR;
D O I
10.1016/j.snb.2018.01.191
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Proteases perform essential functions in a multitude of physiological processes and participate in many human diseases. Probing protease activity sensitively and accurately is critical for both basic research and clinical diagnosis. Herein, a novel optical biosensor for high-sensitive detection of protease was developed based on the specific protease cleavage of synthesized peptide substrate and subsequent assembly between exposed cysteine and Ru(bpy)(3)(2+)-2-cyanobenzothiazole (Ru(bpy)(3)(2+)-CBT). The assembly complexes can be enriched by streptavidin coated magnetic beads on work electrode for high-sensitive electrochemiluminescence (ECL) analysis. Using trypsase and caspase-3 as the examples, the limit of detection (LOD) of 8.4 x 10(-4) UmL(-1) and 5 x 10(-6) UmL(-1) were obtained respectively. This represents one of most sensitive protease assay reported. Current peptide cleavage induced assembly (PCIA) method can be easily extended to detect other proteases by changing peptide substrate sequence, shows its great potential as versatile biosensor in sensing techniques and clinical diagnosis. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:516 / 521
页数:6
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