Target controlled alternative hybridization chain reaction for fluorescent detection of dual mycotoxins

A target controlled alternative hybridization chain reaction (HCR) was developed for fluorescent detection of multiple mycotoxin. Ochratoxin A (OTA) and aflatoxin B1 (AFB1) can bind with their specific aptamer on the gold nanoparticles and cause the releasing of the short DNA sequences. The short DN...

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Published inAnalytica chimica acta Vol. 1237; p. 340595
Main Authors Ma, Qin, Lin, Yiyan, Yang, Yun, Yang, Wenming, Yun, Wen, Zhang, Mingming, Yang, Lizhu
Format Journal Article
LanguageEnglish
Published Elsevier B.V 02.01.2023
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Abstract A target controlled alternative hybridization chain reaction (HCR) was developed for fluorescent detection of multiple mycotoxin. Ochratoxin A (OTA) and aflatoxin B1 (AFB1) can bind with their specific aptamer on the gold nanoparticles and cause the releasing of the short DNA sequences. The short DNA sequences can trigger different reaction route of HCR and thus produce two kinds of side-chain sequences. The side-chain sequences can cause the opening of the DNA tweezers and result the recovery of fluorescent signals. Good linear relationships were obtained in the range of 0.06–2 ng/mL (R2 = 0.994) for OTA and 0.005–1 ng/mL (R2 = 0.992) for AFB1 with limit of detection of 0.02 ng/mL for OTA and 0.002 ng/mL for AFB1. Importantly, it showed great sensitivity and excellent selectivity in practical food sample analysis for simultaneous detection of OTA and AFB1. [Display omitted] •An alternative hybridization chain reaction was developed for dual mycotoxins detection.•The hybridization chain reaction route can be controlled by the target.•This strategy shows promising potentials for simultaneous detection of OTA and AFB1.
AbstractList A target controlled alternative hybridization chain reaction (HCR) was developed for fluorescent detection of multiple mycotoxin. Ochratoxin A (OTA) and aflatoxin B1 (AFB1) can bind with their specific aptamer on the gold nanoparticles and cause the releasing of the short DNA sequences. The short DNA sequences can trigger different reaction route of HCR and thus produce two kinds of side-chain sequences. The side-chain sequences can cause the opening of the DNA tweezers and result the recovery of fluorescent signals. Good linear relationships were obtained in the range of 0.06-2 ng/mL (R2 = 0.994) for OTA and 0.005-1 ng/mL (R2 = 0.992) for AFB1 with limit of detection of 0.02 ng/mL for OTA and 0.002 ng/mL for AFB1. Importantly, it showed great sensitivity and excellent selectivity in practical food sample analysis for simultaneous detection of OTA and AFB1.A target controlled alternative hybridization chain reaction (HCR) was developed for fluorescent detection of multiple mycotoxin. Ochratoxin A (OTA) and aflatoxin B1 (AFB1) can bind with their specific aptamer on the gold nanoparticles and cause the releasing of the short DNA sequences. The short DNA sequences can trigger different reaction route of HCR and thus produce two kinds of side-chain sequences. The side-chain sequences can cause the opening of the DNA tweezers and result the recovery of fluorescent signals. Good linear relationships were obtained in the range of 0.06-2 ng/mL (R2 = 0.994) for OTA and 0.005-1 ng/mL (R2 = 0.992) for AFB1 with limit of detection of 0.02 ng/mL for OTA and 0.002 ng/mL for AFB1. Importantly, it showed great sensitivity and excellent selectivity in practical food sample analysis for simultaneous detection of OTA and AFB1.
A target controlled alternative hybridization chain reaction (HCR) was developed for fluorescent detection of multiple mycotoxin. Ochratoxin A (OTA) and aflatoxin B1 (AFB1) can bind with their specific aptamer on the gold nanoparticles and cause the releasing of the short DNA sequences. The short DNA sequences can trigger different reaction route of HCR and thus produce two kinds of side-chain sequences. The side-chain sequences can cause the opening of the DNA tweezers and result the recovery of fluorescent signals. Good linear relationships were obtained in the range of 0.06–2 ng/mL (R2 = 0.994) for OTA and 0.005–1 ng/mL (R2 = 0.992) for AFB1 with limit of detection of 0.02 ng/mL for OTA and 0.002 ng/mL for AFB1. Importantly, it showed great sensitivity and excellent selectivity in practical food sample analysis for simultaneous detection of OTA and AFB1. [Display omitted] •An alternative hybridization chain reaction was developed for dual mycotoxins detection.•The hybridization chain reaction route can be controlled by the target.•This strategy shows promising potentials for simultaneous detection of OTA and AFB1.
ArticleNumber 340595
Author Yang, Lizhu
Lin, Yiyan
Yang, Yun
Yun, Wen
Ma, Qin
Yang, Wenming
Zhang, Mingming
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Keywords Aflatoxin B1
Hybridization chain reaction
DNA tweezer
Ochratoxin A
Mycotoxin
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Snippet A target controlled alternative hybridization chain reaction (HCR) was developed for fluorescent detection of multiple mycotoxin. Ochratoxin A (OTA) and...
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SubjectTerms Aflatoxin B1
DNA tweezer
Hybridization chain reaction
Mycotoxin
Ochratoxin A
Title Target controlled alternative hybridization chain reaction for fluorescent detection of dual mycotoxins
URI https://dx.doi.org/10.1016/j.aca.2022.340595
https://www.proquest.com/docview/2742658741
Volume 1237
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