Functionalization of gold nanoparticles with amino acid, β-amyloid peptides and fragment

A. Majzik, L. Fülöp, E. Csapó, F. Bogár, T. Martinek, B. Penke, G. Bíró, I. Dékány

Research output: Article

102 Citations (Scopus)

Abstract

Gold nanoparticles (Au NPs) were functionalized by cysteine (Cys), β-amyloid peptides (Cys01-28, Cys01-40, Aβ1-42) and a pentapeptide fragment (Leu-Pro-Phe-Phe-Asp-OH (LPFFD-OH)). Optical absorption spectra of these systems were recorded and the plasmon resonance maximum values (λmax) of the UV-vis spectra together with the transmission electron microscopy (TEM) images were also analysed. Both TEM images and the appearance of a new absorption band between ∼720 and 750nm in the visible spectra of the Au-cysteine and Au-LPFFD-OH systems most probably indicate that upon addition of these molecules to Au NPs-containing aqueous dispersions formation of aggregates is occurred. The wavelength shift between the two observed absorption bands in cysteine- and pentapeptide-modified Au NPs systems are Δλ=185 and 193nm, respectively. These results suggest that the monodisperse spherical gold nanoparticles were arranged to chained structure due to the effect of these molecules. For confirmation of the binding of citrate and cysteine onto the plasmonic metal surface 1H NMR measurements were also performed. 1H NMR results may suggest that the citrate layer on the metal surface is replaced by cysteine leading to a formation of organic double layer structure.In the presence of β-amyloid peptides the aggregation was not observed, especially in the Au-Cys01-40 and Au-Aβ1-42 systems, however compared to the cysteine or LPFFD-OH-containing gold dispersion with Cys01-28 measurable less aggregation were occurred. The spectral parameters clearly suggest that Aβ1-42 can attach or bind to the surface of gold nanoparticles via both the apolar and the N-donors containing side-chains of amino acids and no aggregation in the colloidal gold dispersion was observed.

Original languageEnglish
Pages (from-to)235-241
Number of pages7
JournalColloids and Surfaces B: Biointerfaces
Volume81
Issue number1
DOIs
Publication statusPublished - nov. 1 2010

ASJC Scopus subject areas

  • Biotechnology
  • Surfaces and Interfaces
  • Physical and Theoretical Chemistry
  • Colloid and Surface Chemistry

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