4.8 Article

Hydrogen Peroxide Sensing with Horseradish Peroxidase-Modified Polymer Single Conical Nanochannels

期刊

ANALYTICAL CHEMISTRY
卷 83, 期 5, 页码 1673-1680

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac102795a

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资金

  1. Beilstein-Institut, Frankfurt/Main, Germany
  2. Alexander von Humboldt Foundation
  3. National Science Foundation [CHE 0747237, CMMI 825661]
  4. Deutsche Forschungsgemeinschaft
  5. Bundesministerium fur Bildung und Forschung Germany [Center of Excellence BIOTECmarin]
  6. European Society for Marine Biotechnology
  7. International Human Frontier Science Program
  8. Division Of Chemistry
  9. Direct For Mathematical & Physical Scien [0747237] Funding Source: National Science Foundation

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Inspired from the funtioning and responsiveness of biological ion channels, researchers attempt to develop biosensing systems based on polymer and solid-state nanochannels. The applicability of these nanochannels for detection/sensing of any foreign analyte in the surrounding environment depends critically on the surface characteristics of the inner walls. Attaching recognition sites to the channel walls leads to the preparation of sensors targeted at a specific molecule. There are many nanochannel platforms for the detection of DNA and proteins, but only a few are capable of detecting small molecules. Here, we describe a nanochannel platform for the detection of hydrogen peroxide, H2O2, which is not only a toxic waste product in the cellular systems but also a key player in the redox signaling pathways. The sensor is based on single conical nanochannels fabricated in an ion tracked polymer membrane. The inner walls of the channel are decorated with horseradish peroxidase (HRP) enzyme using carbodiimide coupling chemistry. The success of the HRP immobilization on the channel surface is confirmed by measuring the pH-dependent current voltage (I V) curves of the system. The reported HRP-nanochannel system detects nanomolar concentrations of H2O2 with 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) as the substrate. The immobilized HRP enzyme is thus capable of inducing redox reactions in a subfemtoliter volume of single nanochannels. We demonstrate that functioning of the designed biosensor is reversible and can be used multiple times to detect H2O2 at various concentrations.

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