期刊
ANALYTICA CHIMICA ACTA
卷 1158, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.aca.2021.338413
关键词
Catalytic hairpin assembly; Hybridization chain reaction; Exonuclease III; Homogeneous solution; Double signal fragments
资金
- National Natural Science Foundation of China [U1504216, 21575130]
A novel electrochemical biosensing strategy was proposed to detect CYFRA 21-1 DNA based on Exo III-assisted digestion of DNA polymer, achieving high sensitivity and reliability.
A novel electrochemical biosensing strategy was proposed to detect cytokeratin fragment antigen 21-1 (CYFRA 21-1) DNA based on Exo III-assisted digestion of dsDNA polymer (EADDP) from hybridization chain reaction (HCR). Primarily, the presence of target can drive a catalytic hairpin assembly (CHA) reaction, which was aimed to achieve target recognition and circulation. Then the HCR can be triggered for further signal amplification and generate long dsDNA polymer with signal tags. Subsequently, the introduction of Exo III can digest the long dsDNA polymer to produce large amounts of double signal fragments (DSFs). The above experiments were all carried out in homogeneous solution. Finally, the released DSF can be captured onto the electrode directly by capture probe (CP) and a highly amplified electrochemical signal can be detected. The EADDP in homogeneous solution circumvented complex solid-liquid interface reaction and tedious operation steps on electrode. Besides, one target can be converted into abundant DSFs, which greatly improved the sensitivity. This biosensor exhibited a low detection limit (0.0348 fM) and wide linear range (5 fM similar to 50 nM) for CYFRA 21-1 DNA biosensing with reliable specificity and stability. (c) 2021 Elsevier B.V. All rights reserved.
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