Understanding FRET in Upconversion Nanoparticle Nucleic Acid Biosensors

被引:46
作者
Bhuckory, Shashi [1 ,2 ]
Lahtinen, Satu [3 ]
Hoysniemi, Niina [3 ]
Guo, Jiajia [1 ,4 ]
Qiu, Xue [1 ,5 ,6 ]
Soukka, Tero [3 ]
Hildebrandt, Niko [1 ,7 ,8 ,9 ]
机构
[1] Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CEA, CNRS, F-91198 Gif Sur Yvette, France
[2] NAMSA, EMEA Clin Serv Operat, F-38670 Chasse Sur Rhoone, France
[3] Univ Turku, Dept Life Technol Biotechnol, Turku 20520, Finland
[4] Chinese Acad Sci, Inst Biomed & Hlth Engn, Shenzhen Inst Adv Technol, Bion Sensing & Intelligence Ctr, Shenzhen 518055, Peoples R China
[5] Ocean Univ China, Sch Med & Pharm, Qingdao 266003, Peoples R China
[6] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266237, Peoples R China
[7] Univ Rouen Normandie, Normandie Univ, Lab COBRA Chim Organ Bioorgan React & Anal, CNRS,INSA,UMR6014, F-76000 Rouen, France
[8] Univ Rouen Normandie, Normandie Univ, Lab COBRA Chim Organ Bioorgan React & Anal, CNRS,INSA,FR3038, F-76000 Rouen, France
[9] Seoul Natl Univ, Dept Chem, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
luminescence; upconverting nanocrystals; energy transfer; lanthanides; microRNA; RESONANCE ENERGY-TRANSFER; UPCONVERTING NANOPARTICLES; NANOPHOSPHORS; LUMINESCENCE; IMMUNOASSAY; EXCITATION; CORE; YB3+;
D O I
10.1021/acs.nanolett.2c04899
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Upconversion nanoparticles (UCNPs) have been frequently applied in Fo'rster resonance energy transfer (FRET) bioanalysis. However, the understanding of how surface coatings, bioconjugation, and dye-surface distance influence FRET biosensing performance has not significantly advanced. Here, we investigated UCNPto-dye FRET DNA-hybridization assays in H2O and D2O using similar to 24 nm large NaYF4:Yb3+,Er3+ UCNPs coated with thin layers of silica (SiO2) or poly(acrylic acid) (PAA). FRET resulted in strong distance-dependent PL intensity changes. However, the PL decay times were not significantly altered because of continuous Yb3+-to-Er3+ energy migration during Er3+-to-dye FRET. Direct bioconjugation of DNA to the thin PAA coating combined with the closest possible dye-surface distance resulted in optimal FRET performance with minor influence from competitive quenching by H2O. The better comprehension of UCNP-to-dye FRET was successfully translated into a microRNA (miR-20a) FRET assay with a limit of detection of 100 fmol in a 80 mu L sample volume.
引用
收藏
页码:2253 / 2261
页数:9
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