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CdS quantum dots-based immunoassay combined with particle imprinted polymer technology and laser ablation ICP-MS as a versatile tool for protein detection
T. Vaneckova, J. Bezdekova, M. Tvrdonova, M. Vlcnovska, V. Novotna, J. Neuman, A. Stossova, V. Kanicky, V. Adam, M. Vaculovicova, T. Vaculovic,
Language English Country Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
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- MeSH
- Electrophoresis, Capillary MeSH
- Fluorescence MeSH
- Mass Spectrometry * MeSH
- Immunoassay methods MeSH
- Immunoglobulin G analysis MeSH
- Quantum Dots chemistry MeSH
- Laser Therapy * MeSH
- Molecular Imprinting * MeSH
- Mice MeSH
- Signal Processing, Computer-Assisted MeSH
- Polymers chemistry MeSH
- Proteins analysis MeSH
- Cadmium Compounds chemistry MeSH
- Sulfides chemistry MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
For the first time, the combination of molecularly imprinted polymer (MIP) technology with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is presented with focus on an optimization of the LA-ICP-MS parameters such as laser beam diameter, laser beam fluence, and scan speed using CdS quantum dots (QDs) as a template and dopamine as a functional monomer. A non-covalent imprinting approach was employed in this study due to the simplicity of preparation. Simple oxidative polymerization of the dopamine that creates the self-assembly monolayer seems to be an ideal choice. The QDs prepared by UV light irradiation synthesis were stabilized by using mercaptosuccinic acid. Formation of a complex of QD-antibody and QD-antibody-antigen was verified by using capillary electrophoresis with laser-induced fluorescence detection. QDs and antibody were connected together via an affinity peptide linker. LA-ICP-MS was employed as a proof-of-concept for detection method of two types of immunoassay: 1) antigen extracted from the sample by MIP and subsequently overlaid/immunoreacted by QD-labelled antibodies, 2) complex of antigen, antibody, and QD formed in the sample and subsequently extracted by MIP. The first approach provided higher sensitivity (MIP/NIP), however, the second demonstrated higher selectivity. A mixture of proteins with size in range 10-250 kDa was used as a model sample to demonstrate the capability of both approaches for detection of IgG in a complex sample.
Department of Chemistry Masaryk University Kamenice 753 5 CZ 625 00 Brno Czech Republic
NenoVision s r o Purkynova 649 127 CZ 612 00 Brno Czech Republic
References provided by Crossref.org
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