CdS:Mn quantum dot-functionalized g-C3N4 nanohybrids as signal-generation tags for photoelectrochemical immunoassay of prostate specific antigen coupling DNAzyme concatamer with enzymatic biocatalytic precipitation

被引:220
作者
Zhang, Kangyao [1 ]
Lv, Shuzhen [1 ]
Lin, Zhenzhen [1 ]
Tang, Dianping [1 ]
机构
[1] Fuzhou Univ, Key Lab Anal & Detect Food Safety MOE & Fujian Pr, Collaborat Innovat Ctr Detect Technol Waixi Food, State Key Lab Photocatalysis Energy & Environm,De, Fuzhou 350116, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Photoelectrochemical immunosensor; Mn-doped CdS quantum dots; G-C3N4; nanosheets; Enzyme biocatalytic precipitation; DNAzyme concatamers; Hybridization chain reaction; CARBON NITRIDE NANOSHEETS; AMPLIFICATION STRATEGY; SENSITIVE DETECTION; SENSING PLATFORM; ELECTRON-DONOR; ASCORBIC-ACID; GRAPHENE; ELECTROCATALYSTS; IMMUNOSENSOR; BIOSENSOR;
D O I
10.1016/j.bios.2017.04.005
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new photoelectrochemical (PEC) immunosensor based on Mn-doped CdS quantum dots (CdS:Mn QDs) on g-C3N4 nanosheets was developed for the sensitive detection of prostate specific antibody (PSA) in biological fluids. The signal derived from the as-synthesized Cd:Mn QDs-functionalized g-C3N4 nanohybrids via a hydrothermal method and was amplified through DNAzyme concatamers on gold nanoparticles accompanying enzymatic biocatalytic precipitation. Experimental results by UV-vis absorption spectra and photoluminescence revealed that CdS:Mn QDs/g-C3N4 nanohybrids exhibited higher photocurrent than those of CdS:Mn QDs and g-C3N4 alone. Upon addition of target PSA, a sandwich-type immunoreaction was carried out between capture antibodies and the labeled detection antibodies. Accompanying introduction of gold nanoparticles, the labeled initiator strands on the AuNPs triggered hybridization chain reaction and the formation of DNAzyme concatamers in the presence of hemin. The formed DNAzyme catalyzed 4-chloro-1-naphthol (4-CN) to produce an insoluble/insulating precipitate on the Mn:CdS QDs/g-C3N4, and blocked the light harvesting of Mn:CdS QDs/g-C3N4, thus resulting in the decreasing photocurrent. Under optimal conditions, the immunosensor exhibited good photocurrent responses for determination of target PSA, and allowed detection of PSA at a concentration as low as 3.8 pg mL(-1). The specificity, reproducibility and precision of this system were acceptable. Significantly, this methodology was further evaluated for analyzing human serum samples, giving well-matched results with referenced PSA enzyme-linked immunosorbent assay (ELISA) method.
引用
收藏
页码:34 / 40
页数:7
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