4.8 Article

Photoelectrochemical Sensing of α-Synuclein Based on a AuNPs/Graphdiyne-Modified Electrode Coupled with a Nanoprobe

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 22, Pages 26515-26521

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c07617

Keywords

photoelectrochemistry; graphdiyne; WSe2 nanoflower; nanoprobe; alpha-synuclein

Funding

  1. NSFC [21575073]
  2. Laoshan Scholar Program of Qingdao University of Science and Technology [201802685]

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A sensing method utilizing AuNPs/graphdiyne as low background signal composite material, coupled with a WSe2 nanoflower and nanoprobe for alpha-Syn detection, was developed and exhibited high signal-to-noise ratio, low detection limit, high sensitivity, and good selectivity, showing promising potential in clinical diagnostics.
We developed a method for photoelectrochemical (PEC) sensing based on a AuNPs/graphdiyne, as a low background signal composite material, modified electrode coupled with a nanoprobe (probe DNA/DA/MBA/WSe2) for sensitive alpha-synuclein (alpha-Syn) detection. A tungsten selenide (WSe2) nanoflower was first produced with a one-pot solvothermal method and employed as a signal amplification element and the modified substrate of the nanoprobe. The synergy effect between the WSe2 nanoflower and graphdiyne (GDY) can reduce the photoinduced electron-hole recombination and expedite the spatial charge separation. Due to the synergistic effect of AuNPs/GDY and WSe2, this detection strategy provides a high signal-to-noise ratio and good performance. The signal indicator, dopamine/4-mercaptophenyl boronic acid/WSe2 (DA/MBA/WSe2), was generated with the recognition of boron-diol. In the presence of the a-Syn oligomer, the target triggered cycle I strand displacement amplification and achieved the conversion of the a-Syn oligomer to a massive output of false-target DNA (FT). The output FT was used for the cycle II catalytic hairpin assembly onto the electrode which was modified with AuNPs/GDY and triple-stranded DNA (TsDNA); thereby, plenty of PEC nanoprobes which are composed of probe DNA and the signal indicator are captured, and the photocurrent response is produced correspondingly. This PEC biosensor generated a strong photocurrent with low blank (27.6 nA) and was sensitive to alpha-Syn oligomer. The limit of detection was 3.3 aM, and the relative standard deviation (RSD) was 3.7% at 100 aM. Moreover, it also has good selectivity, indicating promising potential in clinical diagnostics.

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