DNA-mounted self-assembly: New approaches for genomic analysis and SNP detection

被引:25
作者
Bichenkova, Elena V. [1 ]
Lang, Zhaolei [1 ]
Yu, Xuan [1 ]
Rogert, Candelaria [1 ]
Douglas, Kenneth T. [1 ]
机构
[1] Univ Manchester, Sch Pharm & Pharmaceut Sci, Wolfson Ctr Rat Struct Based Design Mol Diagnost, Manchester M13 9PL, Lancs, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2011年 / 1809卷 / 01期
关键词
Polymorphism; Fluorescence; Nanoparticle; Exciplex; Excimer; FRET; NUCLEIC-ACID HYBRIDIZATION; RESONANCE ENERGY-TRANSFER; SINGLE-NUCLEOTIDE POLYMORPHISMS; SEQUENCE COMPOSITION DEPENDENCE; ENHANCED RAMAN-SCATTERING; POINT MUTATIONS; MOLECULAR BEACONS; ACRIDINE-ORANGE; STRANDED-DNA; LABELED DNA;
D O I
10.1016/j.bbagrm.2010.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This article presents an overview of new emerging approaches for nucleic acid detection via hybridization techniques that can potentially be applied to genomic analysis and SNP identification in clinical diagnostics. Despite the availability of a diverse variety of SNP genotyping technologies on the diagnostic market, none has truly succeeded in dominating its competitors thus far. Having been designed for specific diagnostic purposes or clinical applications, each of the existing bio-assay systems (briefly outlined here) is usually limited to a relatively narrow aspect or format of nucleic acid detection, and thus cannot entirely satisfy all the varieties of commercial requirements and clinical demands. This drives the diagnostic sector to pursue novel, cost-effective approaches to ensure rapid and reliable identification of pathogenic or hereditary human diseases. Hence, the purpose of this review is to highlight some new strategic directions in DNA detection technologies in order to inspire development of novel molecular diagnostic tools and bio-assay systems with superior reliability, reproducibility, robustness, accuracy and sensitivity at lower assay cost. One approach to improving the sensitivity of an assay to confidently discriminate between single point mutations is based on the use of target assembled, split-probe systems, which constitutes the main focus of this review. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 23
页数:23
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