A bead-based single nucleotide polymorphism (SNP) detection using melting temperature on a microchip

被引:8
作者
Kao, Pei-Chun [1 ]
Ding, Shih-Torng [2 ]
Lin, En-Chung [2 ]
Li, Kan-Chien [1 ]
Wang, Lon [3 ]
Lu, Yen-Wen [1 ]
机构
[1] Natl Taiwan Univ, Dept Bioind Mechatron Engn, Taipei 10764, Taiwan
[2] Natl Taiwan Univ, Dept Anim Sci, Taipei 10764, Taiwan
[3] Natl Taiwan Univ, Dept Elect Engn, Taipei 10764, Taiwan
关键词
ALLELE-SPECIFIC HYBRIDIZATION; ATAXIA-TELANGIECTASIA; GENOMIC DNA; ATM GENE; CELL; PROBES; GENERATION; ARRAYS; ENZYME;
D O I
10.1007/s10404-014-1331-0
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Single nucleotide polymorphism (SNP) is not only one of the most common genetic variances in a human genome, but it also serves a crucial biomarker greatly affecting the phenotypes of individuals. Moreover, SNP had shown its importance by making contributions in many aspects, including species classification for pests, pesticide resistance detection, and disease diagnostic for human beings. Most of today's SNP detection techniques utilize enzymes or modification of DNA, leading to the requirement of high reagent cost or complex procedures. Therefore, a new SNP genotyping scheme has been developed to address these issues by conducting melting curve analysis on the DNA target sequences, which are conjugated onto polystyrene microbeads in a microfluidic device. The microbeads function as a solid vehicle for capturing the DNA duplexes, providing a larger surface-to-volume ratio for reaction and allowing it to be hydrodynamically confined for melting curve analysis. A prototype device serving as a basis for this proposed scheme was successfully tested, detecting the SNP of ataxia-telangiectasia-mutated gene from both synthetic DNA and genomic DNA of Landrace sows. This bead-based SNP detection only required a minimal reagent amount and simplified the sample preparation procedures, thereby preserving it as a flexible and accurate detection scheme. All these characteristics show great promise in this bead-based SNP detection.
引用
收藏
页码:477 / 488
页数:12
相关论文
共 46 条
  • [1] Apple FS, 1999, CLIN CHEM, V45, P199
  • [2] BOTSTEIN D, 1980, AM J HUM GENET, V32, P314
  • [3] Chen Y.-H., 2008, THESIS NATL TAIWAN U
  • [4] Single-cell enzyme concentrations, kinetics, and inhibition analysis using high-density hydrodynamic cell isolation arrays
    Di Carlo, Dino
    Aghdam, Nima
    Lee, Luke P.
    [J]. ANALYTICAL CHEMISTRY, 2006, 78 (14) : 4925 - 4930
  • [5] Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations
    Dressman, D
    Yan, H
    Traverso, G
    Kinzler, KW
    Vogelstein, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (15) : 8817 - 8822
  • [6] Determining the optimal PDMS-PDMS bonding technique for microfluidic devices
    Eddings, Mark A.
    Johnson, Michael A.
    Gale, Bruce K.
    [J]. JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2008, 18 (06)
  • [7] Solution-based scanning for single-base alterations using a double-stranded DNA binding dye and fluorescence-melting profiles
    Elenitoba-Johnson, KSJ
    Bohling, SD
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (03) : 845 - 853
  • [8] Amplicon melting analysis with labeled primers: A closed-tube method for differentiating homozygotes and heterozygotes
    Gundry, CN
    Vandersteen, JG
    Reed, GH
    Pryor, RJ
    Chen, J
    Wittwer, CT
    [J]. CLINICAL CHEMISTRY, 2003, 49 (03) : 396 - 406
  • [9] Integration of single oocyte trapping, in vitro fertilization and embryo culture in a microwell-structured microfluidic device
    Han, Chao
    Zhang, Qiufang
    Ma, Rui
    Xie, Lan
    Qiu, Tian
    Wang, Lei
    Mitchelson, Keith
    Wang, Jundong
    Huang, Guoliang
    Qiao, Jie
    Cheng, Jing
    [J]. LAB ON A CHIP, 2010, 10 (21) : 2848 - 2854
  • [10] DIFFERENTIAL THERMAL ANALYSIS .3. MELTING CURVES OF OILS AND FATS
    HANNEWIJK, J
    HAIGHTON, AJ
    [J]. JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1958, 35 (09) : 457 - 461