Biomolecular interfaces based on self-assembly and self-recognition form biosensors capable of recording molecular binding and release

Nanoscale. 2019 Mar 14;11(11):4987-4998. doi: 10.1039/c8nr10090j.

Abstract

This research proposed to create the next generation of versatile electrochemical-based biosensors capable of monitoring target capture and release as dictated by molecular binding or unbinding. The biosensor integrates cellular machines (i.e., microtubules, structural elements of cells and kinesin molecular motors involved in cellular transport) as functional units; its assembly is based on molecular self-assembly and self-recognition. Our results demonstrate that the designed biosensor was capable of allowing detection of binding and unbinding events based on redox reactions at user-controlled electrode interfaces. The analysis also showed that the sensitivity of the designed biosensor or its ability to record such events could be user-controlled at any given time by adjusting the energy source that "fuels" the system.

MeSH terms

  • Adenosine Triphosphate
  • Biosensing Techniques / instrumentation*
  • Biosensing Techniques / methods*
  • Electrochemical Techniques
  • Electrodes
  • Kinesins / chemistry
  • Kinesins / metabolism
  • Microtubules / chemistry
  • Microtubules / metabolism
  • Nanotechnology
  • Oxidation-Reduction
  • Protein Binding

Substances

  • Adenosine Triphosphate
  • Kinesins