TY - JOUR
T1 - Upconversion nanoparticles based FRET aptasensor for rapid and ultrasenstive bacteria detection
AU - Jin, Birui
AU - Wang, Shurui
AU - Lin, Min
AU - Jin, Ying
AU - Zhang, Shujing
AU - Cui, Xingye
AU - Gong, Yan
AU - Li, Ang
AU - Xu, Feng
AU - Lu, Tian Jian
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2017/4/15
Y1 - 2017/4/15
N2 - Pathogenic bacteria cause serious harm to human health, which calls for the development of advanced detection methods. Herein, we developed a novel detection platform based on fluorescence resonance energy transfer (FRET) for rapid, ultrasensitive and specific bacteria detection, where gold nanoparticles (AuNPs, acceptor) were conjugated with aptamers while upconversion nanoparticles (UCNPs, donor) were functionalized with corresponding complementary DNA (cDNA). The spectral overlap between UCNPs fluorescence emission and AuNPs absorption enables the occurrence of FRET when hybridizing the targeted aptamer and cDNA, causing upconversion fluorescence quenching. In the presence of target bacteria, the aptamers preferentially bind to bacteria forming a three-dimensional structure and thereby dissociate UCNPs-cDNA from AuNPs-aptamers, resulting in the recovery of upconversion fluorescence. Using the UCNPs based FRET aptasensor, we successfully detected Escherichia coli ATCC 8739 (as a model analyte) with a detection range of 5–106 cfu/mL and detection limit of 3 cfu/mL. The aptasensor was further used to detect E. coli in real food and water samples (e.g., tap/pond water, milk) within 20 min. The novel UCNPs based FRET aptasensor could be used to detect a broad range of targets from whole cells to metal ions by using different aptamer sequences, holding great potential in environmental monitoring, medical diagnostics and food safety analysis.
AB - Pathogenic bacteria cause serious harm to human health, which calls for the development of advanced detection methods. Herein, we developed a novel detection platform based on fluorescence resonance energy transfer (FRET) for rapid, ultrasensitive and specific bacteria detection, where gold nanoparticles (AuNPs, acceptor) were conjugated with aptamers while upconversion nanoparticles (UCNPs, donor) were functionalized with corresponding complementary DNA (cDNA). The spectral overlap between UCNPs fluorescence emission and AuNPs absorption enables the occurrence of FRET when hybridizing the targeted aptamer and cDNA, causing upconversion fluorescence quenching. In the presence of target bacteria, the aptamers preferentially bind to bacteria forming a three-dimensional structure and thereby dissociate UCNPs-cDNA from AuNPs-aptamers, resulting in the recovery of upconversion fluorescence. Using the UCNPs based FRET aptasensor, we successfully detected Escherichia coli ATCC 8739 (as a model analyte) with a detection range of 5–106 cfu/mL and detection limit of 3 cfu/mL. The aptasensor was further used to detect E. coli in real food and water samples (e.g., tap/pond water, milk) within 20 min. The novel UCNPs based FRET aptasensor could be used to detect a broad range of targets from whole cells to metal ions by using different aptamer sequences, holding great potential in environmental monitoring, medical diagnostics and food safety analysis.
KW - Aptamer
KW - E. coli ATCC 8739
KW - Gold nanoparticle
KW - Microorganism detection
KW - Upconversion nanoparticle
UR - https://www.scopus.com/pages/publications/85007043796
U2 - 10.1016/j.bios.2016.10.029
DO - 10.1016/j.bios.2016.10.029
M3 - 文章
C2 - 27825886
AN - SCOPUS:85007043796
SN - 0956-5663
VL - 90
SP - 525
EP - 533
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -