Real-time detection of allele-specific polymerase chain reaction products by automated ultra-thin-layer agarose gel electrophoresis

被引:23
作者
Guttman, A
Barta, C
Szoke, M
Sasvári-Székely, M
Kalász, H
机构
[1] Genet BioSyst Inc, San Diego, CA 92121 USA
[2] Semmelweis Univ, Sch Med, Inst Med Chem Mol & Biol Pathobiochem, Budapest, Hungary
[3] Semmelweis Univ, Sch Med, Inst Pharmacol, Budapest, Hungary
关键词
polymerase chain reaction; ultra-thin-layer agarose gel electrophoresis; DNA;
D O I
10.1016/S0021-9673(98)00814-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ultra-thin-layer agarose gel electrophoresis, a novel combination of agarose slab gel electrophoresis and capillary gel electrophoresis was introduced in conjunction with laser-induced fluorescence (LIF) scanning detection for the analysis of polymerase chain reaction (PCR) products. Allele-specific fragments, amplified from genomic DNA of patients with congenital adrenal hyperplasia (most often caused by mutations of 21-hydroxylase gene, CYP-21), were used as a model system to investigate the applicability, sensitivity and resolving power of the method. The allele-specific products were generated by PCR and separated by ultra-thin-layer agarose gel electrophoresis. The double-stranded DNA fragments were easily visualized in real-time via complexation during the separation process by the intercalator dye TO-PRO-3 which was part of the separation gel-buffer system. In this way, the migrating dsDNA-dye complexes were detected in real-time by a scanning LIF detection system with sub-nanogram sensitivity. The system employs a 632-nm solid-state laser and an avalanche photodiode detector scanning to the separation platform by means of a fiber bundle system. Automated ultra-thin-layer agarose gel electrophoresis with 'on the fly' TO-PRO-3 staining of dsDNA fragments and LIF detection system proved to be a very fast, high-throughput separation method for individual or multiplexed PCR products, with excellent sensitivity. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:481 / 487
页数:7
相关论文
共 13 条
[1]  
Andrews A. T., 1986, ELECTROPHORESIS
[2]   Membrane-mediated sample loading for automated DNA sequencing [J].
Cassel, SM ;
Guttman, A .
ELECTROPHORESIS, 1998, 19 (8-9) :1341-1346
[3]   CAPILLARY GEL AFFINITY ELECTROPHORESIS OF DNA FRAGMENTS [J].
GUTTMAN, A ;
COOKE, N .
ANALYTICAL CHEMISTRY, 1991, 63 (18) :2038-2042
[4]  
Hames B.D., 1990, GEL ELECTROPHORESIS, V2nd Edition, P382
[5]  
Haugland R.P., 1996, Handbook of Fluorescent Probes and Research Chemicals
[6]   CAPILLARY ELECTROPHORESIS OF PROTEINS AND NUCLEIC-ACIDS [J].
KARGER, BL ;
CHU, YH ;
FORET, F .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1995, 24 :579-610
[7]   Analysis of five CFTR mutations in Hungarian cystic fibrosis patients [J].
Nemeth, K ;
Fekete, G ;
Kiss, E ;
Varadi, A ;
Holics, K ;
Ujhelyi, R .
JOURNAL OF INHERITED METABOLIC DISEASE, 1996, 19 (03) :378-378
[8]  
NEW MI, 1990, DEV PHARMACOL THERAP, V15, P200
[9]  
NEWTON CR, 1989, LANCET, V2, P1481
[10]   CAPILLARY ELECTROPHORESIS WITH LASER-INDUCED FLUORESCENCE DETECTION OF PCR FRAGMENTS USING THIAZOLE ORANGE [J].
SCHWARTZ, HE ;
ULFELDER, KJ .
ANALYTICAL CHEMISTRY, 1992, 64 (15) :1737-1740