Fully automated DNA reaction and analysis in a fluidic capillary instrument

被引:67
作者
Swerdlow, H
Jones, BJ
Wittwer, CT
机构
[1] Department of Human Genetics, University of Utah, 308 Biopolymers Bldg. 570, Salt Lake City
[2] Department of Pathology, 5C130 School of Medicine, University of Utah, Salt Lake City
关键词
D O I
10.1021/ac961104o
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple, reliable, automated genetic analysis instrument has been designed and prototyped. The system uses novel fluidic technology, coupling thermal cycling, reaction purification, in-line loading, and capillary electrophoresis in a single instrument. Samples in the loop of an injection valve are amplified inside a rapid air thermal cycler. A liquid chromatographic separation eliminates contaminants and excess salt. The sample is loaded in an efficient, continuous, flow-through manner onto a polymer-filled separation capillary. Detection by laser-induced fluorescence produces signal-to-noise ratios of 1000:1 or greater. Refilling of the polymer-filled capillary is automatic; during the run, the system is reconditioned for injection of another sample. Since all components and connections are fluidic, automation is natural and simple. The instrument is reliable and fast, performing PCR reaction cycling, purification and analysis, all in 20 min. Reproducibility (CV) of retention times is 2% (n = 129) and of peak areas 9% (n = 34). Bubbles and particulates are eliminated by the chromatography column. Adaptation of the instrument prototype for separation of DNA-sequencing reactions is described; cycle sequencing and electrophoresis of a single lane are complete in 90 min. Implications and challenges for development of fully automated fluidic instruments for genomic sequencing are discussed.
引用
收藏
页码:848 / 855
页数:8
相关论文
共 56 条
  • [1] ANDRESEN BD, 1987, Patent No. 4708782
  • [2] Bashkin J, 1996, APPL THEOR ELECTROPH, V6, P23
  • [3] BOCKSTAHLER LE, 1994, PCR METH APPL, V3, P263
  • [4] Butcher A., 1992, Clinical Immunology Newsletter, V12, P73, DOI 10.1016/0197-1859(92)90008-T
  • [5] CAROTHERS AM, 1989, BIOTECHNIQUES, V7, P494
  • [6] Rapid DNA sequencing of more than 1000 bases per run by capillary electrophoresis using replaceable linear polyacrylamide solutions
    Carrilho, E
    RuizMartinez, MC
    Berka, J
    Smirnov, I
    Goetzinger, W
    Miller, AW
    Brady, D
    Karger, BL
    [J]. ANALYTICAL CHEMISTRY, 1996, 68 (19) : 3305 - 3313
  • [7] POLY(ETHYLENEOXIDE) FOR HIGH-RESOLUTION AND HIGH-SPEED SEPARATION OF DNA BY CAPILLARY ELECTROPHORESIS
    CHANG, HT
    YEUNG, ES
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1995, 669 (01): : 113 - 123
  • [8] POST-PCR STERILIZATION - A METHOD TO CONTROL CARRYOVER CONTAMINATION FOR THE POLYMERASE CHAIN-REACTION
    CIMINO, GD
    METCHETTE, KC
    TESSMAN, JW
    HEARST, JE
    ISAACS, ST
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (01) : 99 - 107
  • [9] HIGH-PERFORMANCE CAPILLARY ELECTROPHORESIS USING OPEN TUBES AND GELS
    COHEN, AS
    PAULUS, A
    KARGER, BL
    [J]. CHROMATOGRAPHIA, 1987, 24 : 15 - 24
  • [10] RAPID SEPARATION AND PURIFICATION OF OLIGONUCLEOTIDES BY HIGH-PERFORMANCE CAPILLARY GEL-ELECTROPHORESIS
    COHEN, AS
    NAJARIAN, DR
    PAULUS, A
    GUTTMAN, A
    SMITH, JA
    KARGER, BL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (24) : 9660 - 9663