Tian Huijun, Emrich Charles A, Scherer James R, Mathies Richard A, Andersen Paal Skytt, Larsen Lars Allan, Christiansen Michael
Department of Chemistry, University of California-Berkeley, Berkeley, CA 94720, USA.
Electrophoresis. 2005 May;26(9):1834-42. doi: 10.1002/elps.200410205.
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 PhiX174 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 microCAE device provides the resolution and detection sensitivity required for SSCP analysis, showing its potential for ultrahigh-throughput mutation detection.
对一种高密度384通道微制造毛细管阵列电泳装置进行了评估,用于高通量单链构象多态性(SSCP)分析。采用延迟反向偏置直接电动进样方案,在有效分离长度为8.0厘米的情况下,可提供优于10碱基对的分辨率。PhiX174的HaeIII酶切产物的分离产生了4.0×10⁶的理论塔板数。使用含有10%甘油和15%尿素的5%聚二甲基丙烯酸酯,在两个运行温度(25℃和40℃)下区分了来自与遗传性血色素沉着症(HHC)和遗传性肥厚性心肌病(HCM)相关的HFE、MYL2、MYL3和MYH7基因的21个单核苷酸多态性(SNP),灵敏度达100%。本研究中的数据表明,384通道微CAE装置提供了SSCP分析所需的分辨率和检测灵敏度,显示了其在超高通量突变检测方面的潜力。