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Enhanced Colorimetric Immunoassay Accompanying with Enzyme Cascade Amplification Strategy for Ultrasensitive Detection of Low-Abundance Protein
被引:144
|作者:
Gao, Zhuangqiang
[1
]
Hou, Li
[1
]
Xu, Mingdi
[1
]
Tang, Dianping
[1
]
机构:
[1] Fuzhou Univ, Dept Chem, Minist Educ Key Lab Anal & Detect Food Safety, Fujian Prov Key Lab Anal & Detect Food Safety, Fuzhou 350108, Peoples R China
来源:
SCIENTIFIC REPORTS
|
2014年
/
4卷
基金:
美国国家科学基金会;
中国国家自然科学基金;
关键词:
CANCER BIOMARKER;
GOLD;
NANOPARTICLES;
IMMUNOSENSOR;
RESONANCE;
SIGNAL;
ASSAY;
PALLADIUM;
GRAPHENE;
PLATFORM;
D O I:
10.1038/srep03966
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Methods based on enzyme labels have been developed for colorimetric immunoassays, but most involve poor sensitivity and are unsuitable for routine use. Herein, we design an enhanced colorimetric immunoassay for prostate-specific antigen (PSA) coupling with an enzyme-cascade-amplification strategy (ECAS-CIA). In the presence of target PSA, the labeled alkaline phosphatase on secondary antibody catalyzes the formation of palladium nanostructures, which catalyze 3,3',5,5'-tetramethylbenzidine-H2O2 system to produce the colored products, thus resulting in the signal cascade amplification. Results indicated that the ECAS-CIA presents good responses toward PSA, and allows detection of PSA at a concentration as low as 0.05 ng mL(-1). Intra-and inter-assay coefficients of variation are below 9.5% and 10.7%, respectively. Additionally, the methodology is validated for analysis of clinical serum specimens with consistent results obtained by PSA ELISA kit. Importantly, the ECAS-CIA opens a new horizon for protein diagnostics and biosecurity.
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页数:8
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