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Peptide Functionalized Gold Nanoparticles as a Stimuli Responsive Contrast Medium in Multiphoton Microscopy

Journal article
Authors Johan Borglin
R. Selegard
D. Aili
Marica B Ericson
Published in Nano Letters
Volume 17
Issue 3
Pages 2102-2108
ISSN 1530-6984
Publication year 2017
Published at Department of Chemistry and Molecular Biology
Pages 2102-2108
Language en
Links doi.org/10.1021/acs.nanolett.7b0061...
Keywords Gold nanoparticles, multiphoton microscopy, contrast media, optical sensing, peptide, absorption-induced-luminescence, surface-plasmon resonance, cancer-cells, in-vivo, photoluminescence, diagnostics, nanorods, zinc, nanocrystals, scattering, Chemistry, Science & Technology - Other Topics, Materials Science, Physics
Subject categories Biomaterials Science, Molecular biophysics, Molecular biology

Abstract

There is a need for biochemical contrast mediators with high signal-to-noise ratios enabling noninvasive biomedical sensing, for example, for neural sensing and protein protein interactions, in addition to cancer diagnostics. The translational challenge is to develop a biocompatible approach ensuring high biochemical contrast while avoiding a raise of the background signal. We here present a concept where gold nanoparticles (AuNPs) can be utilized as a stimuli responsive contrast medium by chemically triggering their ability to exhibit multiphoton-induced luminescence (MIL) when performing multiphoton laser scanning microscopy (MPM). Proof-of-principle is demonstrated using peptide-functionalized AuNPs sensitive to zinc ions (Zn2+). Dispersed particles are invisible in the MPM until addition of millimolar concentrations of Zn2+ upon which MIL is enabled through particle aggregation caused by specific peptide interactions and folding. The process can be reversed by removal of the Zn2+ using a chelator, thereby resuspending the AuNPs. In addition, the concept was demonstrated by exposing the particles to matrix metalloproteinase-7 (MMP-7) causing peptide digestion resulting in AuNP aggregation, significantly elevating the MIL signal from the background. The approach is based on the principle that aggregation shifts the plasmon resonance, elevating the absorption cross section in the near-infrared wavelength region enabling onset of MIL. This Letter demonstrates how biochemical sensing can be obtained in far-field MPM and should be further exploited as a future tool for noninvasive optical biosensing.

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