Electrochemical detection of the disease marker human chitinase-3-like protein 1 by matching antibody-modified gold electrodes as label-free immunosensors

被引:13
作者
Chaocharoen, Wethaka [1 ,2 ]
Suginta, Wipa [1 ,2 ]
Limbut, Warakorn [3 ,4 ,5 ]
Ranok, Araya [1 ,2 ]
Numnuam, Apon [3 ,4 ,6 ]
Khunkaewla, Panida [1 ,2 ]
Kanatharana, Proespichaya [3 ,4 ,6 ]
Thavarungkul, Panote [3 ,4 ,7 ]
Schulte, Albert [1 ,2 ]
机构
[1] Suranaree Univ Technol, Biochem Electrochem Res Unit, Sch Chem, Nakhon Ratchasima 30000, Thailand
[2] Suranaree Univ Technol, Biochem Electrochem Res Unit, Sch Biochem, Nakhon Ratchasima 30000, Thailand
[3] Prince Songkla Univ, Trace Anal & Biosensor Res Ctr, Hat Yai 90112, Songkhla, Thailand
[4] Prince Songkla Univ, Ctr Excellence Innovat Chem, Fac Sci, Hat Yai 90112, Songkhla, Thailand
[5] Prince Songkla Univ, Dept Appl Sci, Fac Sci, Hat Yai 90112, Songkhla, Thailand
[6] Prince Songkla Univ, Dept Chem, Fac Sci, Hat Yai 90112, Songkhla, Thailand
[7] Prince Songkla Univ, Dept Phys, Fac Sci, Hat Yai 90112, Songkhla, Thailand
关键词
Human chitinase-3-like protein 1; Chitinase-like proteins; Capacitive immunosensor; Disease marker; Biomarker; CAPACITIVE BIOSENSOR; INFLAMMATORY BIOMARKER; YKL-40; THIOUREA; IMMOBILIZATION;
D O I
10.1016/j.bioelechem.2014.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tissue inflammation, certain cardiovascular syndromes and the occurrence of some solid tumors are correlated with raised serum concentrations of human chitinase-3-like protein 1 (YKL-40), a mammalian chitinase-like glycoprotein, which has become the subject of current research. Here we report the construction and characterization of an electrochemical platform for label-free immunosensing of YKL-40. Details of the synthesis of YKL-40 and production of anti-YKL-40 immunoglobulin G (IgG) are provided and cross-reactivity tests presented. Polyclonal anti-YKL-40 IgG was immobilized on gold electrodes and the resulting immunosensors were operated in an electrochemical flow system with capacitive signal generation. The strategy offered a wide linear detection range (0.1 mu g/L to 1 mg/L) with correlation coefficients (R-2) above 0.99 and good sensitivity (12.28 +/- 0.27 nF/cm(2) per decade of concentration change). Additionally, the detection limit of 0.07 +/- 0.01 mu g/L was well below that of optical enzyme-linked immunosorbent assays (ELISAs), which makes the proposed methodology a promising alternative for YKL-40 related disease studies. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:106 / 113
页数:8
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