1. Detection of a cancer biomarker protein on modified cellulose paper by fluorescence using aptamer-linked quantum dots
- Author
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Pradip Das and Ulrich J. Krull
- Subjects
Paper ,Aptamer ,Oligonucleotides ,010402 general chemistry ,01 natural sciences ,7. Clean energy ,Biochemistry ,Analytical Chemistry ,chemistry.chemical_compound ,Complementary DNA ,Quantum Dots ,Biomarkers, Tumor ,Fluorescence Resonance Energy Transfer ,Electrochemistry ,Animals ,Humans ,Environmental Chemistry ,Bovine serum albumin ,Cellulose ,Spectroscopy ,Detection limit ,biology ,010401 analytical chemistry ,Serum Albumin, Bovine ,Epithelial cell adhesion molecule ,Buffer solution ,Epithelial Cell Adhesion Molecule ,Fluorescence ,Molecular biology ,Neoplasm Proteins ,0104 chemical sciences ,Förster resonance energy transfer ,chemistry ,Biophysics ,biology.protein ,Cattle - Abstract
The development of point-of-care bioassays for sensitive screening of protein-based cancer biomarkers would improve the opportunity for early stage diagnosis. A strategy for a fluorescence resonance energy transfer (FRET)-based bioassay has been investigated that makes use of modified cellulose paper for the detection of an epithelial cell adhesion molecule (EpCAM), which is a transmembrane glycoprotein that is overexpressed in several tumors of epithelial origin. The paper matrix was a substrate for immobilized aptamer-linked quantum dots (QDs-Apt) and Cy3 labeled complementary DNA (cDNA), which served as a donor and an acceptor, respectively. Competitive binding of EpCAM displaced the cDNA, resulting in the reduction of FRET. The paper-based bioassay was able to detect EpCAM in buffer solution as well as in 10% bovine serum solution using a reaction time of no more than 60 minutes. The dynamic range was 1-100 nM in buffer with a precision better than 4%, and the limit of detection was 250 pM in buffer and 600 pM in 10% serum.
- Published
- 2017
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