纳米传感器
费斯特共振能量转移
荧光
纳米颗粒
DNA
化学
核酸
生物物理学
胶体金
纳米技术
分子信标
猝灭(荧光)
材料科学
寡核苷酸
生物化学
生物
物理
量子力学
作者
Shulian Bai,Bangtian Xu,Yongcan Guo,Juhui Qiu,Wenhao Yu,Guoming Xie
出处
期刊:Theranostics
[Ivyspring International Publisher]
日期:2018-01-01
卷期号:8 (9): 2424-2434
被引量:16
摘要
While detection of microRNA with or without signal amplification is highly informative, nanosensors with high specificity for cell-specific RNA detection are rare. Methods: In this study, a tetrahedral DNA nanostructure (TDN) with a specific function was combined with gold nanoparticles (Au-NP) possessing fluorescence quenching effects and a large surface area to fabricate a fluorescence resonance energy transfer based nanosensor (Au-TDNN). The presence of miR-21 (target) can separate the fluorescent dye-labeled detection probe on Au-TDNNs from Au-NPs, which separates the donor and acceptor, thus inducing an intensive fluorescence signal. High specificity for discerning point mutation targets was achieved by rationally designing the nucleic acid strand displacement reaction to occur spontaneously with ΔG0 ≈ 0 based on thermodynamic parameters; under this condition, slight thermodynamic changes caused by base mismatch exert significant effects on hybridization yield. Results: Chemically synthesized DNA of three single-base-changed analogues of target, let-7d, and miR-200b were tested. A discrimination factor (DF) of 15.4 was produced by the expected detection probe on Au-NPs for proximal single-base mismatch. As the control group, the DF produced by an ordinary detection probe on Au-NPs only reached 2.4. The feasibility of the proposed strategy was also confirmed using hepatocyte cancer cells (HepG2). Conclusion: This improved nanosensor opens a new avenue for the specific and easy detection of microRNA in live cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI