Magnetic beads–assisted fluorescence aptasensing approach based on dual DNA tweezers for detection of ochratoxin A and fumonisin B1 in wine and corn
A magnetic beads (MBs)–assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of ochratoxin A (OTA) and fumonisin B 1 (FB 1 ). A dual DNA tweezers structure with four ends linked with fluorophores (FAM, ROX) and quenchers (BHQ...
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Published in | Analytical and bioanalytical chemistry Vol. 413; no. 26; pp. 6677 - 6685 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.11.2021
Springer Nature B.V |
Subjects | |
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Abstract | A magnetic beads (MBs)–assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of ochratoxin A (OTA) and fumonisin B
1
(FB
1
). A dual DNA tweezers structure with four ends linked with fluorophores (FAM, ROX) and quenchers (BHQ
1
, BHQ
2
) was designed, and produced the high initial fluorescence signals because of the long spatial distance between FAM and BHQ
1
, ROX, and BHQ
2
. Bio-aptamer/anti-aptamer of OTA and bio-aptamer/anti-aptamer of FB
1
were respectively annealed to form dsDNA, and immobilized to MBs coated with streptavidin (SA). With the existence of OTA and FB
1
, OTA and FB
1
preferentially bound with their respective bio-aptamers, which made anti-aptamers dissociate from dsDNA coupled on MBs. After magnetic separation, the dissociated anti-aptamers reacted with dual DNA tweezers, respectively, which made DNA tweezers close and the fluorescence was quenched. The linear ranges of approach for OTA and FB
1
detection were 0.05–20 ng/mL and 0.1–40 ng/mL, respectively. The limit of detection for OTA and FB
1
was 0.029 ng/mL and 0.061 ng/mL. The prepared MBs-assisted fluorescence aptasensing approach was applied to detect OTA and FB
1
in spiked red wine and corn samples, which showed good recoveries between 92 and 106%. |
---|---|
AbstractList | A magnetic beads (MBs)–assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of ochratoxin A (OTA) and fumonisin B1 (FB1). A dual DNA tweezers structure with four ends linked with fluorophores (FAM, ROX) and quenchers (BHQ1, BHQ2) was designed, and produced the high initial fluorescence signals because of the long spatial distance between FAM and BHQ1, ROX, and BHQ2. Bio-aptamer/anti-aptamer of OTA and bio-aptamer/anti-aptamer of FB1 were respectively annealed to form dsDNA, and immobilized to MBs coated with streptavidin (SA). With the existence of OTA and FB1, OTA and FB1 preferentially bound with their respective bio-aptamers, which made anti-aptamers dissociate from dsDNA coupled on MBs. After magnetic separation, the dissociated anti-aptamers reacted with dual DNA tweezers, respectively, which made DNA tweezers close and the fluorescence was quenched. The linear ranges of approach for OTA and FB1 detection were 0.05–20 ng/mL and 0.1–40 ng/mL, respectively. The limit of detection for OTA and FB1 was 0.029 ng/mL and 0.061 ng/mL. The prepared MBs-assisted fluorescence aptasensing approach was applied to detect OTA and FB1 in spiked red wine and corn samples, which showed good recoveries between 92 and 106%. A magnetic beads (MBs)-assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of ochratoxin A (OTA) and fumonisin B1 (FB1). A dual DNA tweezers structure with four ends linked with fluorophores (FAM, ROX) and quenchers (BHQ1, BHQ2) was designed, and produced the high initial fluorescence signals because of the long spatial distance between FAM and BHQ1, ROX, and BHQ2. Bio-aptamer/anti-aptamer of OTA and bio-aptamer/anti-aptamer of FB1 were respectively annealed to form dsDNA, and immobilized to MBs coated with streptavidin (SA). With the existence of OTA and FB1, OTA and FB1 preferentially bound with their respective bio-aptamers, which made anti-aptamers dissociate from dsDNA coupled on MBs. After magnetic separation, the dissociated anti-aptamers reacted with dual DNA tweezers, respectively, which made DNA tweezers close and the fluorescence was quenched. The linear ranges of approach for OTA and FB1 detection were 0.05-20 ng/mL and 0.1-40 ng/mL, respectively. The limit of detection for OTA and FB1 was 0.029 ng/mL and 0.061 ng/mL. The prepared MBs-assisted fluorescence aptasensing approach was applied to detect OTA and FB1 in spiked red wine and corn samples, which showed good recoveries between 92 and 106%.A magnetic beads (MBs)-assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of ochratoxin A (OTA) and fumonisin B1 (FB1). A dual DNA tweezers structure with four ends linked with fluorophores (FAM, ROX) and quenchers (BHQ1, BHQ2) was designed, and produced the high initial fluorescence signals because of the long spatial distance between FAM and BHQ1, ROX, and BHQ2. Bio-aptamer/anti-aptamer of OTA and bio-aptamer/anti-aptamer of FB1 were respectively annealed to form dsDNA, and immobilized to MBs coated with streptavidin (SA). With the existence of OTA and FB1, OTA and FB1 preferentially bound with their respective bio-aptamers, which made anti-aptamers dissociate from dsDNA coupled on MBs. After magnetic separation, the dissociated anti-aptamers reacted with dual DNA tweezers, respectively, which made DNA tweezers close and the fluorescence was quenched. The linear ranges of approach for OTA and FB1 detection were 0.05-20 ng/mL and 0.1-40 ng/mL, respectively. The limit of detection for OTA and FB1 was 0.029 ng/mL and 0.061 ng/mL. The prepared MBs-assisted fluorescence aptasensing approach was applied to detect OTA and FB1 in spiked red wine and corn samples, which showed good recoveries between 92 and 106%. A magnetic beads (MBs)–assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of ochratoxin A (OTA) and fumonisin B₁ (FB₁). A dual DNA tweezers structure with four ends linked with fluorophores (FAM, ROX) and quenchers (BHQ₁, BHQ₂) was designed, and produced the high initial fluorescence signals because of the long spatial distance between FAM and BHQ₁, ROX, and BHQ₂. Bio-aptamer/anti-aptamer of OTA and bio-aptamer/anti-aptamer of FB₁ were respectively annealed to form dsDNA, and immobilized to MBs coated with streptavidin (SA). With the existence of OTA and FB₁, OTA and FB₁ preferentially bound with their respective bio-aptamers, which made anti-aptamers dissociate from dsDNA coupled on MBs. After magnetic separation, the dissociated anti-aptamers reacted with dual DNA tweezers, respectively, which made DNA tweezers close and the fluorescence was quenched. The linear ranges of approach for OTA and FB₁ detection were 0.05–20 ng/mL and 0.1–40 ng/mL, respectively. The limit of detection for OTA and FB₁ was 0.029 ng/mL and 0.061 ng/mL. The prepared MBs-assisted fluorescence aptasensing approach was applied to detect OTA and FB₁ in spiked red wine and corn samples, which showed good recoveries between 92 and 106%. A magnetic beads (MBs)–assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of ochratoxin A (OTA) and fumonisin B 1 (FB 1 ). A dual DNA tweezers structure with four ends linked with fluorophores (FAM, ROX) and quenchers (BHQ 1 , BHQ 2 ) was designed, and produced the high initial fluorescence signals because of the long spatial distance between FAM and BHQ 1 , ROX, and BHQ 2 . Bio-aptamer/anti-aptamer of OTA and bio-aptamer/anti-aptamer of FB 1 were respectively annealed to form dsDNA, and immobilized to MBs coated with streptavidin (SA). With the existence of OTA and FB 1 , OTA and FB 1 preferentially bound with their respective bio-aptamers, which made anti-aptamers dissociate from dsDNA coupled on MBs. After magnetic separation, the dissociated anti-aptamers reacted with dual DNA tweezers, respectively, which made DNA tweezers close and the fluorescence was quenched. The linear ranges of approach for OTA and FB 1 detection were 0.05–20 ng/mL and 0.1–40 ng/mL, respectively. The limit of detection for OTA and FB 1 was 0.029 ng/mL and 0.061 ng/mL. The prepared MBs-assisted fluorescence aptasensing approach was applied to detect OTA and FB 1 in spiked red wine and corn samples, which showed good recoveries between 92 and 106%. |
Author | He, Xing Zhao, Luyang Qu, Chenling Yu, Songcheng Wei, Min |
Author_xml | – sequence: 1 givenname: Chenling surname: Qu fullname: Qu, Chenling email: quchenling82@163.com organization: College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology – sequence: 2 givenname: Luyang surname: Zhao fullname: Zhao, Luyang organization: College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology – sequence: 3 givenname: Xing surname: He fullname: He, Xing organization: College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology – sequence: 4 givenname: Songcheng surname: Yu fullname: Yu, Songcheng organization: College of Public Health, Zhengzhou University – sequence: 5 givenname: Min surname: Wei fullname: Wei, Min email: wei_min80@163.com organization: College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology |
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Copyright | Springer-Verlag GmbH Germany, part of Springer Nature 2021 Springer-Verlag GmbH Germany, part of Springer Nature 2021. 2021. Springer-Verlag GmbH Germany, part of Springer Nature. |
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Keywords | Fumonisin B Dual DNA tweezers Detection MBs-assisted fluorescence aptasensing approach Ochratoxin A |
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Snippet | A magnetic beads (MBs)–assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of... A magnetic beads (MBs)-assisted fluorescence aptasensing approach based on dual DNA tweezers and magnetic separation was established for the detection of... |
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SubjectTerms | Analytical Chemistry Aptamers Beads Biochemistry Characterization and Evaluation of Materials Chemical compounds Chemistry Chemistry and Materials Science Corn Deoxyribonucleic acid detection limit DNA DNA structure Fluorescence fluorescent dyes Fluorophores Food Food Science Fumonisin B1 Laboratory Medicine Magnetic separation magnetism Monitoring/Environmental Analysis Ochratoxin A Public health red wines Research Paper Sensors Streptavidin Wine |
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Title | Magnetic beads–assisted fluorescence aptasensing approach based on dual DNA tweezers for detection of ochratoxin A and fumonisin B1 in wine and corn |
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