Detection of a cancer biomarker protein on modified cellulose paper by fluorescence using aptamer-linked quantum dots

被引:36
作者
Das, Pradip [1 ]
Krull, Ulrich J. [1 ]
机构
[1] Univ Toronto, Chem Sensors Grp, Dept Chem & Phys Sci, 3359 Mississauga Rd North, Mississauga, ON L5L 1C6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
NUCLEIC-ACID HYBRIDIZATION; RESONANCE ENERGY-TRANSFER; CELL ADHESION MOLECULE; SIGNAL AMPLIFICATION; MICROFLUIDIC DEVICES; CHALLENGES; DONORS; OPPORTUNITIES; BIOANALYSIS; DIAGNOSTICS;
D O I
10.1039/c7an00624a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
收藏
页码:3132 / 3135
页数:4
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