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High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device
被引:35
|作者:
Tian, HJ
Emrich, CA
Scherer, JR
Mathies, RA
[1
]
Andersen, PS
Larsen, LA
Christiansen, M
机构:
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Biophys Grad Grp, Berkeley, CA 94720 USA
[3] Univ Copenhagen, State Serum Inst, Dept Clin Biochem, DK-1168 Copenhagen, Denmark
[4] Univ Copenhagen, Wilhelm Johannsen Ctr Funct Genome Res, Dept Med Biochem & Genet, DK-1168 Copenhagen, Denmark
[5] Copenhagen Heart Arrythmia Res Ctr, Copenhagen, Denmark
关键词:
capillary array electrophoresis;
genotyping;
hereditary hemochromatosis;
hereditary hypertrophic cardiomyopathy;
microfabrication miniaturization;
single-strand conformation polymorphism;
D O I:
10.1002/elps.200410205
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
A high-density 384-lane microfabricated capillary array electrophoresis device is evaluated for high-throughput single-strand conformation polymorphism (SSCP) analysis. A delayed back bias direct electrokinetic injection scheme is used to provide better than 10-bp resolution with an 8.0-cm effective separation length. Separation of a HaeIII digest of phi X174 yielded theoretical plate numbers of 4.0 x 10(6). Using 5% PDMA containing 10% glycerol and 15% urea, 21 single-nucleotide polymorphisms (SNPs) from HFE, MYL2, MYL3, and MYH7 genes associated with hereditary hemochromatosis (HHC) and hereditary hypertrophic cardiomyopathy (HCM) are discriminated at two running temperatures (25 degrees C and 40 degrees C), providing 100% sensitivity. The data in this study demonstrate that the 384-lane mu CAE device provides the resolution and detection sensitivity required for SSCP analysis, showing its potential for ultrahigh-throughput mutation detection.
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页码:1834 / 1842
页数:9
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