Highly Selective Cerebral ATP Assay Based on Micrometer Scale Ion Current Rectification at Polyimidazolium-Modified Micropipettes

Anal Chem. 2017 Jun 20;89(12):6794-6799. doi: 10.1021/acs.analchem.7b01218. Epub 2017 May 31.

Abstract

Development of new principles and methods for cerebral ATP assay is highly imperative not only for determining ATP dynamics in brain but also for understanding physiological and pathological processes related to ATP. Herein, we for the first time demonstrate that micrometer scale ion current rectification (MICR) at a polyimidazolium brush-modified micropipette can be used as the signal transduction output for the cerebral ATP assay with a high selectivity. The rationale for ATP assay is essentially based on the competitive binding ability between positively charged polyimidazolium and ATP toward negatively charged ATP aptamer. The method is well responsive to ATP with a good linearity within a concentration range from 5 nM to 100 nM, and high selectivity toward ATP. These properties essentially enable the method to determine the cerebral ATP by combining in vivo microdialysis. The basal dialysate level of ATP in rat brain cortex is determined to be 11.32 ± 2.36 nM (n = 3). This study demonstrates that the MICR-based sensors could be potentially used for monitoring neurochemicals in cerebral systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / analysis*
  • Adenosine Triphosphate / metabolism
  • Animals
  • Aptamers, Nucleotide / chemistry
  • Aptamers, Nucleotide / metabolism
  • Binding, Competitive
  • Brain / metabolism*
  • Electric Conductivity
  • Electrochemical Techniques / methods*
  • Electrodes
  • Imidazoles / chemistry
  • Male
  • Microdialysis / instrumentation
  • Microdialysis / methods*
  • Polymers / chemistry
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Aptamers, Nucleotide
  • Imidazoles
  • Polymers
  • imidazole
  • Adenosine Triphosphate