Sensitive detection of p53 tumor suppressor gene using an enzyme-based solid-state electrochemiluminescence sensing platform

被引:39
作者
Wang, Xiaoying [1 ]
Zhang, Xiangyi [1 ]
He, Pingang [2 ]
Fang, Yuzhi [2 ]
机构
[1] Southeast Univ, Sch Publ Hlth, Dept Hyg Analyt Chem, Key Lab Environm Med & Engn,Minist Educ, Nanjing 210009, Peoples R China
[2] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
关键词
MWNTs-Ru(bpy)(3)(2+) composite; Solid-state electrochemiluminescence; Glucose-dehydrogenase; Wild type p53 sequence; Muted type p53 sequence; ELECTROGENERATED CHEMILUMINESCENCE; ALCOHOL-DEHYDROGENASE; IMMUNOHISTOCHEMICAL DETECTION; HYBRIDIZATION DETECTION; DNA HYBRIDIZATION; GOLD; BIOSENSOR; RU(BPY)(3)(2+); MONOLAYERS; PROTEIN;
D O I
10.1016/j.bios.2011.02.012
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An enzyme-based solid-state electrochemiluminescence (ECL) sensing platform for sensitive detection of a single point mutation is developed successfully using p53 tumor suppressor gene as a model analyte. A composite of multiwalled carbon nanotubes and Ruthenium (II) tris-(bipyridine)(MWNTs-Ru(bpy)(3)(2+)) was prepared and coated on an electrode surface, which was covered by polypyrrole (PPy) to immobilize ssDNA. Then, the ssDNA recognized the gold nanoparticle (AuNP)-labeled p53 tumor suppressor gene, and produced AuNP-dsDNA electrode with AuNP layer. The surface adsorbed the glucose-dehydrogenase (GDH) molecules for producing ECL signal. This system combined enzyme reaction with ECL detection, and it can recognize sequence-specific wild type p53 sequence (wtp53) and muted type p53 sequence (mtp53) with discrimination of up to 56.3%. The analytic results were sensitive and specific. It holds promise for the diagnosis and management of cancer. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:3608 / 3613
页数:6
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