Kinetic analysis of human metallothionein and CdTe quantum dot complexes using fluorescence and voltammetry techniques

Colloids Surf B Biointerfaces. 2017 Dec 1:160:381-389. doi: 10.1016/j.colsurfb.2017.09.033. Epub 2017 Sep 14.

Abstract

Thanks to quantum dots' (QDs) properties, they can be used as selective and sensitive biomarkers in molecular imaging. In a previous paper, we confirmed the possibility of interaction between mercaptosuccinic acid-capped cadmium telluride QDs (MSA-CdTe) and human metallothionein (MT). The aim of this study was to expand on our previous research with an evaluation of the stability of the formed complexes between human MT and four CdTe compounds of the following sizes: 3.4nm (blue QDs), 3.8nm (green QDs), 4.5nm (yellow QDs), and 5.2nm (red QDs). Complexes were evaluated over time using fluorescence intensity and differential pulse voltammetry. Differences between the voltammograms obtained for standard solutions and for CdTe+MT show that complexes were formed. An increase in fluorescence intensity was observed for blue (Δ%≈40 for t=1→120min) and red (Δ%≈30 for t=1→120min) CdTe-MT complexes than CdTe alone, whereas green and yellow CdTe-MT complexes had a lower fluorescence intensity than CdTe alone. A stronger time dependence of the mercaptosuccinic acid (MSA) peak height on the timeline and differences in the MSA peak shape (in CdTe, and CdTe+MT complexes) were also observed by voltammetry. Authors noticed a decrease in the Cat2 signal of the red and green CdTe+MT complexes at the time of conjugation. Our results reveal that the size of QDs has an impact on the interaction between CdTe and human MT, as well as on the stability of complexes formed during these interactions. The bioconjugates' stability was also found to depend on the time of interaction.

Keywords: Bioconjugation; Biomarkers; Differential pulse voltammetry; Electrochemistry; Metallothionein; Quantum dots.

MeSH terms

  • Cadmium Compounds / chemistry*
  • Cadmium Compounds / metabolism
  • Electrochemical Techniques / methods*
  • Fluorescence
  • Humans
  • Kinetics
  • Metallothionein / chemistry*
  • Metallothionein / metabolism
  • Protein Binding
  • Quantum Dots*
  • Spectrometry, Fluorescence / methods*
  • Tellurium / chemistry*
  • Tellurium / metabolism
  • Time Factors

Substances

  • Cadmium Compounds
  • Metallothionein
  • Tellurium
  • cadmium telluride