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High-Throughput Low-Background G-Quadruplex Aptamer Chemiluminescence Assay for Ochratoxin A Using a Single Photonic Crystal Microsphere.
Shen, Peng; Li, Wei; Liu, Yan; Ding, Zhi; Deng, Yang; Zhu, Xuerui; Jin, Yanhao; Li, Yichen; Li, Jianlin; Zheng, Tiesong.
Afiliação
  • Shen P; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Li W; Department of Electronic and Electrical Engineering, The University of Sheffield , Sheffield S3 7HQ, United Kingdom.
  • Liu Y; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Ding Z; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Deng Y; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Zhu X; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Jin Y; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Li Y; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Li J; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
  • Zheng T; Department of Food Science and Engineering, Nanjing Normal University , Nanjing 210024, China.
Anal Chem ; 89(21): 11862-11868, 2017 11 07.
Article em En | MEDLINE | ID: mdl-28988477
ABSTRACT
We reported a novel hemin-G-quadruplex aptamer chemiluminescence assay platform for ochratoxin A (OTA) using the single silica photonic crystal microsphere (SPCM). The oligonucleotide A sequence containing aptamer sequences of hemin and OTA is immobilized on the surface of SPCM. The other oligonucleotide B sequence containing a partially complementary sequence with one part OTA aptamer and one part hemin aptamer is used as a blocking chain. The hybridization between chain A and chain B will be influenced by the presence or absence of OTA in the system, which will affect the bioactivity of DNAzyme. Thus, the chemiluminescence signal depends on the concentration of OTA in the samples. In the single particle assay platform, the signal/noise is remarkably enhanced, and the background signal can be ignored by separating hemin from the surface of SPCM. The limit of detection of the new method reaches to the pg/mL scale, and the linear detection range is 4 orders of magnitude for OTA. The new assay platform can provide a sensitive, cost-efficient, simple, and high-throughput screening for OTA.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Aptâmeros de Nucleotídeos / Quadruplex G / Ocratoxinas Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Aptâmeros de Nucleotídeos / Quadruplex G / Ocratoxinas Idioma: En Ano de publicação: 2017 Tipo de documento: Article