TY - JOUR
T1 - Real time PCR based on fluorescent quenching of mercaptoacetic acid-modified cdte quantum dots for ultrasensitive specific detection of nucleic acids
AU - Cui, Daxiang
AU - Li, Qing
AU - Huang, Peng
AU - Wang, Kan
AU - Kong, Yifei
AU - Zhang, Hong
AU - You, Xiaogang
AU - He, Rong
AU - Song, Hua
AU - Wang, Jingping
AU - Bao, Chenchen
AU - Asahi, Toru
AU - Gao, Feng
AU - Osaka, Tetsuya
N1 - Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2010
Y1 - 2010
N2 - A ultra-sensitive, highly specific, real-time polymerase chain reaction system based on mercaptoacetic acid-modified CdTe nanocrystals(mQDs) is reported. With the addition of 3 nm mQDs into the PCR reagent, the photoluminescent(PL) intensities of mQDs decreased gradually as the DNA templates and PCR cycles increased, in an approximate negative linear relation to the DNA concentration logarithm or cycles, the PL peaks exhibited red-shifts synchronously. Mg2+ ions decreased the PL intensity of mQDs in a dose-dependent means, and Taq DNA polymerase enhanced the PL intensity of mQDs in a dose-dependent means. Real-time PCR based on mQDs showed an increased sensitivity at least 103 fold higher than that based on SYBR Green I. The specificity of PCR was enhanced in the PCR reagent with less than 1.33mg/mL mQDs. The potential mechanism is also discussed. This novel PCR system based on mQDs has great potential in applications such as ultra-sensitive specific DNA or RNA detection, dynamic molecular imaging, and photoelectric biosensors.
AB - A ultra-sensitive, highly specific, real-time polymerase chain reaction system based on mercaptoacetic acid-modified CdTe nanocrystals(mQDs) is reported. With the addition of 3 nm mQDs into the PCR reagent, the photoluminescent(PL) intensities of mQDs decreased gradually as the DNA templates and PCR cycles increased, in an approximate negative linear relation to the DNA concentration logarithm or cycles, the PL peaks exhibited red-shifts synchronously. Mg2+ ions decreased the PL intensity of mQDs in a dose-dependent means, and Taq DNA polymerase enhanced the PL intensity of mQDs in a dose-dependent means. Real-time PCR based on mQDs showed an increased sensitivity at least 103 fold higher than that based on SYBR Green I. The specificity of PCR was enhanced in the PCR reagent with less than 1.33mg/mL mQDs. The potential mechanism is also discussed. This novel PCR system based on mQDs has great potential in applications such as ultra-sensitive specific DNA or RNA detection, dynamic molecular imaging, and photoelectric biosensors.
KW - Mercaptoacetic acid-modified cdte quantum dot
KW - Photoluminescence
KW - Polymerase chain reaction
KW - Sensitivity
KW - Specificity
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U2 - 10.5101/nbe.v2i1.p44-54
DO - 10.5101/nbe.v2i1.p44-54
M3 - Article
AN - SCOPUS:79551666907
SN - 2150-5578
VL - 2
SP - 45
EP - 55
JO - Nano Biomedicine and Engineering
JF - Nano Biomedicine and Engineering
IS - 1
ER -