A microfluidic system for large DNA molecule arrays

被引:151
作者
Dimalanta, ET
Lim, A
Runnheim, R
Lamers, C
Churas, C
Forrest, DK
de Pablo, JJ
Graham, MD
Coppersmith, SN
Goldstein, S
Schwartz, DC
机构
[1] Univ Wisconsin, Lab Mol & Computat Genom, Dept Chem, Madison, WI 53706 USA
[2] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Chem Engn, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Phys, Madison, WI 53706 USA
关键词
D O I
10.1021/ac0496401
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Single molecule approaches offer the promise of large, exquisitely miniature ensembles for the generation of equally large data sets. Although microfluidic devices have previously been designed to manipulate single DNA molecules, many of the functionalities they embody are not applicable to very large DNA molecules, normally extracted from cells. Importantly, such microfluidic devices must work within an integrated system to enable high-throughput biological or biochemical analysis-a key measure of any device aimed at the chemical/biological interface and required if large data sets are to be created for subsequent analysis. The challenge here was to design an integrated microfluidic device to control the deposition or elongation of large DNA molecules (up to millimeters in length), which would serve as a general platform for biological/biochemical analysis to function within an integrated system that included massively parallel data collection and analysis. The approach we took was to use replica molding to construct silastic devices to consistently deposit oriented, elongated DNA molecules onto charged surfaces, creating massive single molecule arrays, which we analyzed for both physical and biochemical insights within an integrated environment that created large data sets. The overall efficacy of this approach was demonstrated by the restriction enzyme mapping and identification of single human genomic DNA molecules.
引用
收藏
页码:5293 / 5301
页数:9
相关论文
共 45 条
[1]  
Anantharaman T, 1999, Proc Int Conf Intell Syst Mol Biol, P18
[2]   Genomics via optical mapping .2. Ordered restriction maps [J].
Anantharaman, TS ;
Mishra, B ;
Schwartz, DC .
JOURNAL OF COMPUTATIONAL BIOLOGY, 1997, 4 (02) :91-118
[3]  
Aston C, 1999, METHOD ENZYMOL, V303, P55
[4]   Physics and applications of microfluidics in biology [J].
Beebe, DJ ;
Mensing, GA ;
Walker, GM .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :261-286
[5]   ALIGNMENT AND SENSITIVE DETECTION OF DNA BY A MOVING INTERFACE [J].
BENSIMON, A ;
SIMON, A ;
CHIFFAUDEL, A ;
CROQUETTE, V ;
HESLOT, F ;
BENSIMON, D .
SCIENCE, 1994, 265 (5181) :2096-2098
[6]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[7]   An integrated nanoliter DNA analysis device [J].
Burns, MA ;
Johnson, BN ;
Brahmasandra, SN ;
Handique, K ;
Webster, JR ;
Krishnan, M ;
Sammarco, TS ;
Man, PM ;
Jones, D ;
Heldsinger, D ;
Mastrangelo, CH ;
Burke, DT .
SCIENCE, 1998, 282 (5388) :484-487
[8]   ORDERED RESTRICTION-ENDONUCLEASE MAPS OF YEAST ARTIFICIAL CHROMOSOMES CREATED BY OPTICAL MAPPING ON SURFACES [J].
CAI, WW ;
ABURATANI, H ;
STANTON, VP ;
HOUSMAN, DE ;
WANG, YK ;
SCHWARTZ, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) :5164-5168
[9]  
Cantor CR, 1980, BIOPHYSICAL CHEM 2
[10]   Patterned deposition of cells and proteins onto surfaces by using three-dimensional microfluidic systems [J].
Chiu, DT ;
Jeon, NL ;
Huang, S ;
Kane, RS ;
Wargo, CJ ;
Choi, IS ;
Ingber, DE ;
Whitesides, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2408-2413