?-shaped fiber optic LSPR biosensor based on mismatched hybridization chain reaction and gold nanoparticles for detection of circulating cell-free DNA

被引:26
|
作者
Ning, Wei [1 ]
Zhang, Chuyan [2 ]
Tian, Ziyi [1 ]
Wu, Mengfan [3 ]
Luo, Zewei [3 ]
Hu, Shunming [1 ]
Pan, Hongzhi [4 ]
Li, Yongxin [1 ]
机构
[1] Sichuan Univ, West China Sch Publ Hlth, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Med Equipment Innovat Res Ctr, Precis Med Ctr,MedX Ctr Mfg, Chengdu 610041, Peoples R China
[3] Sichuan Univ, Res Ctr Analyt Instrumentat, Sch Mech Engn, Chengdu 610065, Peoples R China
[4] Shanghai Univ Med & Hlth Sci, Affiliated Zhoupu Hosp, Shanghai 201318, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Fiber optic; Localized surface plasmon resonance; Mismatched hybridization chain reaction; Gold nanoparticles; Cell -free DNA; NUCLEIC-ACIDS; CANCER; TOOL; AMPLIFICATION; BLOOD; PCR;
D O I
10.1016/j.bios.2023.115175
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Circulating cell-free DNA (cfDNA) is a promising biomarker of liquid biopsy, but it still faces some difficulties in achieving sensitive and convenient detection. Herein, an omega-shaped fiber optic localized surface plasmon resonance (FO-LSPR) biosensor based on hybridization chain reaction (HCR) coupled with gold nanoparticles (AuNPs) was developed, and applied in simple and sensitive detection of cfDNA. Specifically, one-base mismatch was designed in HCR hairpins (H1 and H2) to obtain high reaction efficiency, and AuNPs was introduced onto H1 through poly-adenine to construct HCR coupled with AuNPs strategy. Meanwhile, target cfDNA was designed into two domains: one could trigger HCR to generate dsDNA concatemer carrying numerous AuNPs, and the other could hybridize with capture DNA on the surface of omega-shaped fiber optic (FO) probes. Thus, the presence of target cfDNA would initiate HCR, and bring the formed dsDNA concatemer and AuNPs to approach the probe surface, resulting in dramatically amplified LSPR signal. Besides, HCR required simple isothermal and enzymefree condition, and omega-shaped FO probe with high refractive index sensitivity just needed to be immersed into HCR solution directly for signal monitoring. Benefiting from the synergetic amplification of mismatched HCR and AuNPs, the proposed biosensor exhibited high sensitivity with a limit of detection of 14.0 pM, and therefore could provide a potential strategy for biomedical analysis and disease diagnosis.
引用
收藏
页数:7
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