Electrochemical analysis of HIV-1 reverse transcriptase serum level: exploiting protein binding to a functionalized nanostructured surface

Talanta. 2011 Jul 15;85(1):770-8. doi: 10.1016/j.talanta.2011.04.070. Epub 2011 May 5.

Abstract

This manuscript describes an electrochemical approach to the detection of the reverse transcriptase of the human immunodeficiency virus type-1 (HIV-1 RT) in serum exploiting an organometallic peptide conjugate that is chemically linked to a nanostructured gold surface. The assay format is based on the formation of a thin film of a ferrocene-labeled lipoic acid (Fc-LA) onto a gold nanoparticles-functionalized screen-printed carbon electrode (GNPs-SPCE). Time-of-Flight secondary ion mass spectrometry (TOF-SIMS) and X-ray photoelectron spectroscopy were employed to confirm the binding of the Fc-LA to the electrode surface via formation of a gold-thiol bond. The RT biosensor was developed by covalent attachment of the peptide VEAIIRILQQLLFIH to the carboxylic acid group of Fc-LA. Square wave voltammetry offered a two-dimensional measurement of RT based on the anodic shift and reduction of current density of the Fc redox signal upon binding of RT to its specific peptide. This allowed a linear quantification of the target RT in the range of 1-500 pg mL(-1) equivalent to 0.9-427 fM, with a detection limit of 0.8 pg mL(-1) (0.7 fM) with a short response time.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques / methods*
  • Electrochemical Techniques / methods*
  • Ferrous Compounds
  • HIV Reverse Transcriptase / blood*
  • Humans
  • Limit of Detection
  • Metallocenes
  • Nanostructures / chemistry*
  • Peptides
  • Protein Binding
  • Thioctic Acid

Substances

  • Ferrous Compounds
  • Metallocenes
  • Peptides
  • Thioctic Acid
  • reverse transcriptase, Human immunodeficiency virus 1
  • HIV Reverse Transcriptase
  • ferrocene