Journal
SCIENTIFIC REPORTS
Volume 7, Issue -, Pages -Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/srep42740
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Funding
- Hong Kong Baptist University [FRG2/15-16/002]
- Health and Medical Research Fund [HMRF/14130522]
- Research Grants Council [HKBU/12301115, HKBU/204612, HKBU/201913]
- French Agence Nationale de la Recherche/Research Grants Council Joint Research Scheme [AHKBU201/12, Oligoswitch ANR-12-IS07-0001]
- National Natural Science Foundation of China [21575121, 21628502]
- Guangdong Province Natural Science Foundation [2015A030313816]
- Hong Kong Baptist University Century Club Sponsorship Scheme
- Interdisciplinary Research Matching Scheme [RC-IRMS/15-16/03]
- Science and Technology Development Fund, Macao SAR [098/2014/A2]
- University of Macau [MYRG2015-00137-ICMS-QRCM, MYRG2016-00151-ICMS-QRCM, MRG044/LCH/2015/ICMS]
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A novel iridium(III) complex was prepared and used as a conductor for sensitive and enzyme-free electrochemical detection of interferon gamma (IFN-gamma). This assay is based on a dual signal amplification mechanism involving positively charged gold nanoparticles ((+) AuNPs) and hybridization chain reaction (HCR). To construct the sensor, nafion (Nf) and (+) AuNPs composite membrane was first immobilized onto the electrode surface. Subsequently, a loop-stem structured capture probe (CP) containing a special IFN-gamma interact strand was modified onto the (+) AuNP surface via the formation of Au-S bonds. Upon addition of IFN-gamma, the loop-stem structure of CP was opened, and the newly exposed sticky region of CP then hybridized with DNA hairpin-1 (H-1), which in turn opened its hairpin structure for hybridizing with DNA hairpin-2 (H-2). Happen of HCR between H-1 and H-2 thus generated a polymeric duplex DNA (dsDNA) chain. Meanwhile, the iridium(III) complex could interact with the grooves of the dsDNA polymer, producing a strong current signal that was proportional to IFN-gamma concentration. Thus, sensitive detection of IFN-gamma could be realized with a detection limit down to 16.3 fM. Moreover, satisfied results were achieved by using this method for the detection of IFN-gamma in human serum samples.
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