A bombykol electrochemical receptor sensor and its kinetics

Bioelectrochemistry. 2019 Aug:128:263-273. doi: 10.1016/j.bioelechem.2019.04.009. Epub 2019 Apr 23.

Abstract

This study aimed to explore the interaction between bombykol and BmOR1 and also provide a paradigm for agroforestry pest control. The electrochemical biosensor signal amplification system was used: nanogold with horseradish peroxidase. An electrochemical bilayer nanogold membrane receptor sensor was developed using the following schemes and processes: twice self-assembly of nanogold and succeeding absorption of Bombyx mori olfactory receptor 1 (BmOR1); sex pheromone-binding protein; spectral scanning and transmission electron microscope to characterize nanogold sol; and atomic force microscope, cyclic voltammetry, and AC impedance methods to characterize individual processes of sensor assembly. The amperometric I-T curve was adopted to measure the response current upon interaction with different concentrations of bombykol (diluted in phosphate-buffered saline) and BmOR1. The results demonstrated the receptor-ligand interaction pattern, which was similar to enzymatic reaction kinetics, with the activation constant Ka of up to 8.57 × 10-20 mol/L and signal magnification of about 10,000-fold. In this study, the simulation of intracellular receptor signaling cascade by an electrochemical signal amplification system helped in directly measuring BmOR1-bombykol ligand interaction and exploring the kinetics after the self-assembly of BmOR1 on the biosensor. It provided a novel platform for future studies on receptor-ligand interaction.

Keywords: Bombykol; Electrochemical receptor biosensor; Electrochemical signal amplification system; GPCRs; Ligand interaction kinetics.

MeSH terms

  • Animals
  • Biosensing Techniques
  • Bombyx
  • Electrochemical Techniques / methods*
  • Fatty Alcohols / metabolism*
  • GTP-Binding Proteins / metabolism
  • Horseradish Peroxidase / metabolism
  • Kinetics
  • Limit of Detection
  • Receptors, Cell Surface / metabolism*

Substances

  • Fatty Alcohols
  • Receptors, Cell Surface
  • bombykol
  • Horseradish Peroxidase
  • GTP-Binding Proteins