A highly sensitive peptide-based biosensor using NiCo2O4 nanosheets and g-C3N4 nanocomposite to construct amplified strategy for trypsin detection

被引:23
作者
Lin, Yanyu [1 ]
Shen, Rongkai [2 ]
Liu, Nannan [1 ]
Yi, Huan [3 ]
Dai, Hong [1 ]
Lin, Jianhua [2 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat, Fujian Prov Key Lab Adv Mat Oriented Chem Engn, Fuzhou 350108, Fujian, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Fuzhou 350002, Fujian, Peoples R China
[3] Fujian Med Univ, Affiliated Hosp, Fujian Prov Matern & Childrens Hosp, Fuzhou 350108, Fujian, Peoples R China
基金
美国国家科学基金会;
关键词
NiCo2O4; nanosheets; Peptide-based sensor; Trypsin; g-C3N4; nanocomposite; ELECTROCHEMICAL IMMUNOSENSOR; NANOPARTICLES;
D O I
10.1016/j.aca.2018.06.040
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Here, a simple electrochemical biosensor was proposed based on the specific recognition between trypsin and peptide. Initially, NiCo2O4-PAMAM nanocomposite was casted on the bare electrode to achieve the electrochemical signal amplification in 0.1 mM [Ru(NH3)(6)](3+) solution owing to the great electronic conductivity and high electrochemical activity induced by the special structure of NiCo2O4 nanosheets (Ni3+ cations in octachedral sites of the Co3O4). Subsequently, a declined electrochemical signal was obtained when g-C3N4 labeled peptide composites were anchored on the electrode. However, after trypsin was added into solution and incubated with the biosensor, the electrochemical signal was re-promoted. Therefore, the as-synthesized biosensor could realize the sensitive detection of trypsin by virtue of the specific recognition between trypsin and peptide. As a result, the developed peptide-based exhibited a linear range from 10(-10) to 10(-4) mg mL(-1) with an ultralow detection limit of 10(-10) mg mL(-1), providing sensitive analytical performance and acceptable application potential in clinical test and disease diagnosis due to its high stability, excellent selectivity, acceptable reproducibility and accurate signal output. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 183
页数:9
相关论文
共 24 条
[1]   A novel optical nanoprobe for trypsin detection and inhibitor screening based on Mn-doped ZnSe quantum dots [J].
Gao, Xue ;
Tang, Guangchao ;
Li, Yang ;
Su, Xingguang .
ANALYTICA CHIMICA ACTA, 2012, 743 :131-136
[2]   Nickel Cobaltite Nanostructures with Enhanced Supercapacitance Activity [J].
Garg, Neha ;
Basu, Mrinmoyee ;
Ganguli, Ashok Kumar .
JOURNAL OF PHYSICAL CHEMISTRY C, 2014, 118 (31) :17332-17341
[3]   Synthesis of graphene supported graphene-like C3N4 metal-free layered nanosheets for enhanced electrochemical performance and their biosensing for biomolecules [J].
Gu, Hui ;
Zhou, Tianshu ;
Shi, Guoyue .
TALANTA, 2015, 132 :871-876
[4]   Peptide-templated gold nanoclusters as a novel label-free biosensor for the detection of protease activity [J].
Gu, Yi ;
Wen, Qian ;
Kuang, Yongqing ;
Tang, Lijuan ;
Jiang, Jianhui .
RSC ADVANCES, 2014, 4 (27) :13753-13756
[5]   Au nanoparticles/PAMAM dendrimer functionalized wired ethyleneamine-viologen as highly efficient interface for ultra-sensitive α-fetoprotein electrochemical immunosensor [J].
Kavosi, Begard ;
Hallaj, Rahman ;
Teymourian, Hazhir ;
Salimi, Abdollah .
BIOSENSORS & BIOELECTRONICS, 2014, 59 :389-396
[6]  
Marvin R.M. H, 1957, ANAL CHEM, V29, P3
[7]   Highly sensitive, label-free colorimetric assay of trypsin using silver nanoparticles [J].
Miao, Peng ;
Liu, Tao ;
Li, Xiaoxi ;
Ning, Limin ;
Yin, Jian ;
Han, Kun .
BIOSENSORS & BIOELECTRONICS, 2013, 49 :20-24
[8]   Peptic and tryptic digestion of peptides and proteins monitored by capillary electrophoresis with contactless conductivity detection [J].
Schuchert-Shi, Aiping ;
Hauser, Peter C. .
ANALYTICAL BIOCHEMISTRY, 2009, 387 (02) :202-207
[9]   A SPECTROPHOTOMETRIC DETERMINATION OF TRYPSIN AND CHYMOTRYPSIN [J].
SCHWERT, GW ;
TAKENAKA, Y .
BIOCHIMICA ET BIOPHYSICA ACTA, 1955, 16 (04) :570-575
[10]   High sensitive trypsin activity evaluation applying a nanostructured QCM-sensor [J].
Stoytcheva, M. ;
Zlatev, R. ;
Cosnier, S. ;
Arredondo, M. ;
Valdez, B. .
BIOSENSORS & BIOELECTRONICS, 2013, 41 :862-866