4.8 Article

A DNA nanopillar as a scaffold to regulate the ratio and distance of mimic enzymes for an efficient cascade catalytic platform

期刊

CHEMICAL SCIENCE
卷 12, 期 1, 页码 407-411

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc03584j

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资金

  1. NNSF of China [21974108, 21775124, 21675129]
  2. Fundamental Research Funds for the Central Universities [XDJK2019B022, XDJK2020TY002]
  3. Chongqing Natural Science Foundation [cstc2018jcyjAX0085]

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This study utilized a rigid 3D DNA nanopillar to investigate the influence of spatial organization on cascade activity in multienzyme systems, achieving controllable regulation of mimic enzyme ratio and spacing. The results demonstrate that the optimal mimic enzyme ratio can be obtained by adjusting the DNA polyhedron structure, and the constructed DNA nanopillar supports directional movement of a bipedal DNA walker for continuous enzyme spacing regulation.
Herein, a rigid 3D DNA nanopillar was used to investigate the influence of spatial organization on the cascade activity in multienzyme systems, realizing controllable regulation of the mimic enzyme ratio and spacing for acquiring a high-efficiency enzyme cascade catalytic platform. Initially, the ratio of mimic enzyme AuNPs (glucose oxidase-like activity) and hemin/G-quadruplex DNAzyme (peroxidase-like activity) fixed at the designed position was adjusted by changing the number of edges in a DNA polyhedron, resulting in an optimal mimic enzyme ratio of 1 : 4 with a quadrangular prism as the scaffold. Notably, the DNA nanopillar formed by quadrangular prism layer-by-layer assembly acted as a track for directional and controllable movement of a bipedal DNA walker based on the toehold mediated strand displacement reaction (TSDR), which endowed the assay system with continuous enzyme spacing regulation compared with previous enzyme cascade systems that induced inflexible operation. Furthermore, enzyme mimetics in this work circumvented the drawbacks of natural enzymes, such as time-consuming purification processes and poor thermal stability. As a proof of concept, the proposed dual regulation strategy of cascade enzymes was applied in the ultrasensitive electrochemical detection of Pb2+, which provided a new route to fabrication of high-performance artificial enzyme cascade platforms for ultimate application in bioanalysis and biodiagnostics.

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