Redox Host-Guest Nanosensors Installed with DNA Gatekeepers for Immobilization-Free and Ratiometric Electrochemical Detection of miRNA.
Xiyue XieZhenqiang WangMeizhen ZhouYuxin XingYuhua ChenJixi HuangKaiyong CaiJixi HuangPublished in: Small methods (2021)
Electrochemical nanosensors by integrating functional nucleic acids and nanomaterials hold a great promise in the fast detection of biomarkers, yet the current systems possess limitations on the accessibility of target-probe and probe-electrode interactions and the repeatability of detection. Herein, a host-guest assembly strategy is developed to build redox nanosensors for an immobilization-free and ratiometric electrochemical detection system. Specifically, electroactive molecule (E m ) guests are loaded in porous hosts of polydopamine nanoparticles (MPDA) to act as dual-signal redox reporters. Hybrid DNA probes of G-quadruplex and a single-stranded anchor DNA are installed as gatekeepers for sealing the mesopores. Thereby, miRNA triggered E m release by strand displacement reactions and the homogeneous transportation of the hosts/guests to the electrode facilitate the generation of reference signal/response signal at different potentials. Concomitantly applied NIR irradiation boosts the electron transfer from MPDA to the electrode and results in a tenfold increase in the reference signal. Finally, the sensing system through the differential pulse voltammetry method achieves a highly repeatable detection (relative standard deviation 3.8%) of miRNA with a lower detection limit (362 × 10 -15 m). This attractive system paves the way for rational designs of advanced electrochemical biosensors and smart diagnosis.
Keyphrases
- label free
- electron transfer
- loop mediated isothermal amplification
- real time pcr
- living cells
- gold nanoparticles
- ionic liquid
- fluorescent probe
- circulating tumor
- cell free
- photodynamic therapy
- drug delivery
- molecularly imprinted
- hydrogen peroxide
- radiation therapy
- sensitive detection
- blood pressure
- binding protein
- mass spectrometry
- circulating tumor cells
- artificial intelligence
- highly efficient
- simultaneous determination