Microfluidic extraction, stretching and analysis of human chromosomal DNA from single cells

被引:51
作者
Benitez, Jaime J. [1 ]
Topolancik, Juraj [1 ]
Tian, Harvey C. [4 ]
Wallin, Christopher B. [1 ]
Latulippe, David R. [1 ]
Szeto, Kylan [1 ]
Murphy, Patrick J. [2 ]
Cipriany, Benjamin R. [5 ]
Levy, Stephen L. [3 ]
Soloway, Paul D. [2 ]
Craighead, Harold G. [1 ]
机构
[1] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Nutr Sci, Ithaca, NY 14853 USA
[3] SUNY Binghamton, Dept Phys Appl Phys & Astron, Binghamton, NY 13902 USA
[4] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[5] Cornell Univ, Dept Elect & Comp Engn, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
MOLECULE DETECTION; MICROCHIP; PURIFICATION; PLATFORMS; GENOME;
D O I
10.1039/c2lc40955k
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a microfluidic device for the extraction, purification and stretching of human chromosomal DNA from single cells. A two-dimensional array of micropillars in a microfluidic polydimethylsiloxane channel was designed to capture a single human cell. Megabase-long DNA strands released from the cell upon lysis are trapped in the micropillar array and stretched under optimal hydrodynamic flow conditions. Intact chromosomal DNA is entangled in the array, while other cellular components are washed from the channel. To demonstrate the entrapment principle, a single chromosome was hybridized to whole chromosome paints, and imaged by fluorescence microscopy. DNA extracted from a single cell and small cell populations (less than 100) was released from the device by restriction endonuclease digestion under continuous flow and collected for off-chip analysis. Quantification of the extracted material reveals that the microdevice efficiently extracts essentially all chromosomal DNA. The device described represents a novel platform to perform a variety of analyses on chromosomal DNA at the single cell level.
引用
收藏
页码:4848 / 4854
页数:7
相关论文
共 32 条
[1]  
Alberts B., 2002, The shape and structure of proteins, Vfourth, DOI 10.1093/aob/mcg023
[2]  
Appasani K, 2011, STEM CELLS BIOL REG, P3, DOI 10.1007/978-1-60761-860-7_1
[3]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[4]   THE ROLE OF DNA FRAGMENTATION IN APOPTOSIS [J].
BORTNER, CD ;
OLDENBURG, NBE ;
CIDLOWSKI, JA .
TRENDS IN CELL BIOLOGY, 1995, 5 (01) :21-26
[5]   DNA mapping using microfluidic stretching and single-molecule detection of fluorescent site-specific tags [J].
Chan, EY ;
Goncalves, NM ;
Haeusler, RA ;
Hatch, AJ ;
Larson, JW ;
Maletta, AM ;
Yantz, GR ;
Carstea, ED ;
Fuchs, M ;
Wong, GG ;
Gullans, SR ;
Gilmanshin, R .
GENOME RESEARCH, 2004, 14 (06) :1137-1146
[6]   Single Molecule Epigenetic Analysis in a Nanofluidic Channel [J].
Cipriany, Benjamin R. ;
Zhao, Ruqian ;
Murphy, Patrick J. ;
Levy, Stephen L. ;
Tan, Christine P. ;
Craighead, Harold G. ;
Soloway, Paul D. .
ANALYTICAL CHEMISTRY, 2010, 82 (06) :2480-2487
[7]   Droplet-based microfluidic platforms for the encapsulation and screening of mammalian cells and multicellular organisms [J].
Clausell-Tormos, Jenifer ;
Lieber, Diana ;
Baret, Jean-Christophe ;
El-Harrak, Abdeslam ;
Miller, Oliver J. ;
Frenz, Lucas ;
Blouwolff, Joshua ;
Humphry, Katherine J. ;
Koster, Sarah ;
Duan, Honey ;
Holtze, Christian ;
Weitz, David A. ;
Griffiths, Andrew D. ;
Merten, Christoph A. .
CHEMISTRY & BIOLOGY, 2008, 15 (05) :427-437
[8]   REPTATION OF A POLYMER CHAIN IN PRESENCE OF FIXED OBSTACLES [J].
DEGENNES, PG .
JOURNAL OF CHEMICAL PHYSICS, 1971, 55 (02) :572-+
[9]   DNA fragment sizing by single molecule detection in submicrometer-sized closed fluidic channels [J].
Foquet, M ;
Korlach, J ;
Zipfel, W ;
Webb, WW ;
Craighead, HG .
ANALYTICAL CHEMISTRY, 2002, 74 (06) :1415-1422
[10]   Magnetic bead handling on-chip: new opportunities for analytical applications [J].
Gijs, MAM .
MICROFLUIDICS AND NANOFLUIDICS, 2004, 1 (01) :22-40