On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors

ACS Sens. 2017 Dec 22;2(12):1767-1773. doi: 10.1021/acssensors.7b00692. Epub 2017 Nov 27.

Abstract

Porous silicon (PSi) nanomaterials have been widely studied as label-free optical biosensors for protein detection. However, these biosensors' performance, specifically in terms of their sensitivity (which is typically in the micromolar range), is insufficient for many applications. Herein, we present a proof-of-concept application of the electrokinetic isotachophoresis (ITP) technique for real-time preconcentration of a target protein on a PSi biosensor. With ITP, a highly concentrated target zone is delivered to the sensing area, where the protein target is captured by immobilized aptamers. The detection of the binding events is conducted in a label-free manner by reflective interferometric Fourier transformation spectroscopy (RIFTS). Up to 1000-fold enhancement in local concentration of the protein target and the biosensor's sensitivity are achieved, with a measured limit of detection of 7.5 nM. Furthermore, the assay is successfully performed in complex media, such as bacteria lysate samples, while the selectivity of the biosensor is retained. The presented assay could be further utilized for other protein targets, and to promote the development of clinically useful PSi biosensors.

Keywords: aptamer; isotachophoresis; label-free; optical biosensor; porous silicon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aptamers, Nucleotide / chemistry
  • Biosensing Techniques / instrumentation
  • Biosensing Techniques / methods*
  • Escherichia coli K12
  • Glycoside Hydrolases / analysis*
  • Glycoside Hydrolases / chemistry
  • Isotachophoresis / methods
  • Lab-On-A-Chip Devices
  • Limit of Detection
  • Peptide Fragments / analysis*
  • Peptide Fragments / chemistry
  • Porosity
  • Protein Domains
  • Sensitivity and Specificity
  • Silicon / chemistry*
  • Spectrophotometry / methods

Substances

  • Aptamers, Nucleotide
  • Peptide Fragments
  • Glycoside Hydrolases
  • arabinan endo-1,5-alpha-L-arabinosidase
  • Silicon