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Detection of the most common corneal dystrophies caused by BIGH3 gene point mutations using a multispot gold-capped nanoparticle array chip.

Authors
 So Young Yoo  ;  Do-Kyun Kim  ;  Tae Jung Park  ;  Eung Kweon Kim  ;  Eiichi Tamiya  ;  Sang Yup Lee 
Citation
 ANALYTICAL CHEMISTRY, Vol.82(4) : 1349-1357, 2010 
Journal Title
 ANALYTICAL CHEMISTRY 
ISSN
 0003-2700 
Issue Date
2010
MeSH
Base Sequence ; Corneal Diseases/diagnosis* ; Corneal Diseases/genetics* ; DNA/chemistry ; DNA/genetics ; DNA Probes/chemistry ; DNA Probes/genetics ; Extracellular Matrix Proteins/genetics* ; Gold/chemistry* ; Homozygote ; Humans ; Metal Nanoparticles/chemistry* ; Nucleic Acid Hybridization ; Oligonucleotide Array Sequence Analysis/instrumentation ; Oligonucleotide Array Sequence Analysis/methods* ; Point Mutation* ; Surface Plasmon Resonance ; Time Factors ; Transforming Growth Factor beta/genetics*
Abstract
The localized surface plasmon resonance (LSPR) optical property has recently been well employed as an effective platform for the quantitative detection of protein-protein interactions on the nanoscale. However, its advantage has not been fully explored yet in the DNA diagnosis field, especially in detecting point mutations of DNA. Point mutations of the BIGH3 gene are associated with the most common corneal dystrophies (CDs), such as Avellino corneal dystrophy, Reis-Bucklers corneal dystrophy, and lattice corneal dystrophy. Since the detection of these corneal dystrophies is urgently needed before laser-assisted in situ keratomileusis operation to prevent blindness, genetic analysis of the BIGH3 gene is critical in most ophthalmological clinics. In this study, we report LSPR-based detection of the BIGH3 gene mutations by using a multispot gold-capped nanoparticle array (MG-NPA) chip. The analytical range and sensitivity of the MG-NPA chip were determined by measuring different concentrations of each CD target DNA in the range of 1 fM to 1 microM. Under the optimal conditions, the detection of DNA hybridization with each CD target DNA was performed with a detection limit of 1 pM target DNA. The selective discrimination against a single-base mismatch DNA sequence was also achieved by using both homozygous and heterozygous CD samples. It demonstrates that the label-free LSPR-based optical biosensor system employing the MG-NPA chip provides a new diagnostic platform allowing the selective and sensitive detection of various DNA point mutations, leading to possible diagnosis of mutation-related diseases including corneal dystrophies reported here.
Full Text
http://pubs.acs.org/doi/abs/10.1021/ac902410z
DOI
10.1021/ac902410z
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Ophthalmology (안과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Eung Kweon(김응권) ORCID logo https://orcid.org/0000-0002-1453-8042
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/100631
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