SERS Assay for Copper(II) Ions Based on Dual Hot-Spot Model Coupling with MarR Protein: New Cu2+-Specific Biorecognition Element

Anal Chem. 2017 Jun 20;89(12):6392-6398. doi: 10.1021/acs.analchem.6b05106. Epub 2017 Jun 8.

Abstract

We have developed a rapid and ultrasensitive surface-enhanced Raman scattering (SERS) assay for Cu2+ detection using the multiple antibiotic resistance regulator (MarR) as specific bridging molecules in a SERS hot-spot model. In the assay, Cu2+ induces formation of MarR tetramers, which provide Au nanoparticle (NP)-AuNP bridges, resulting in the formation of SERS hot spots. 4-Mercaptobenzoic acid (4-MBA) was used as a Raman reporter. The addition of Cu2+ increased the Raman intensity of 4-MBA. Use of a dual hot-spot signal-amplification strategy based on AuNP-AgNP heterodimers combined through antigen-antibody reactions increased the sensitivity of the sensing platform by 50-fold. The proposed method gave a linear response for Cu2+ detection in the range of 0.5-1000 nM, with a detection limit of 0.18 nM, which is 5 orders of magnitude lower than the U.S. Environmental Protection Agency limit for Cu2+ in drinking water (20 μM). In addition, all analyses can be completed in less than 15 min. The high sensitivity, high specificity, and rapid detection capacity of the SERS assay therefore provide a combined advantage over current assays.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Copper / analysis*
  • Escherichia coli Proteins / chemistry*
  • Ions / analysis
  • Repressor Proteins / chemistry*
  • Spectrum Analysis, Raman
  • Surface Properties

Substances

  • Escherichia coli Proteins
  • Ions
  • MarR protein, E coli
  • Repressor Proteins
  • Copper