Abstract |
Surface enhanced Raman scattering (SERS) is highly useful for sensitive analytical sensing; however, its practical availability for detecting a point mutation associated with disease in clinical sample was rarely proved. Herein, we present a toehold-mediated, DNA displacement-based, SERS sensor for detecting point mutations in the BIGH3 gene associated with the most common corneal dystrophies (CDs) in a clinical setting. To diagnose Avellino corneal dystrophy (ACD), selectivity was ensured by exploring optimal DNA displacement conditions such as length of toehold and hybridization temperature. A SERS-efficient Ag@Au bimetallic nanodendrite was employed to ensure sensitivity. Optimization for a clinical setting showed that discrimination was maximized when toehold length was 6-mer (T6), and hybridization temperature was 36 °C. On the basis of tests that used clinical homozygous and heterozygous CD samples, a single-base mismatched DNA sequence was identifiable within 30 min with a limit of detection (LOD) of 400 fM. From the results, we conclude that our toehold-mediated, DNA displacement-based, SERS sensor allows a rapid and sensitive detection of a BIGH3 gene point mutation associated with Avellino corneal dystrophy, indicating the practical ability of the method to diagnose genetic diseases caused by point mutations.
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Authors | Saetbyeol Kim, Su-Nam Jeong, Sangsu Bae, Hoeil Chung, So Young Yoo |
Journal | Analytical chemistry
(Anal Chem)
Vol. 88
Issue 23
Pg. 11288-11292
(12 06 2016)
ISSN: 1520-6882 [Electronic] United States |
PMID | 27934116
(Publication Type: Letter, Research Support, Non-U.S. Gov't)
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Chemical References |
- Extracellular Matrix Proteins
- Transforming Growth Factor beta
- betaIG-H3 protein
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Topics |
- Corneal Dystrophies, Hereditary
(genetics)
- Extracellular Matrix Proteins
(genetics)
- Humans
- Point Mutation
- Spectrum Analysis, Raman
- Surface Properties
- Transforming Growth Factor beta
(genetics)
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