The potential and challenges of nanopore sequencing

被引:1968
作者
Branton, Daniel [1 ]
Deamer, David W. [2 ]
Marziali, Andre [3 ]
Bayley, Hagan [4 ]
Benner, Steven A. [5 ]
Butler, Thomas [6 ]
Di Ventra, Massimiliano [7 ]
Garaj, Slaven [8 ]
Hibbs, Andrew [9 ]
Huang, Xiaohua [10 ]
Jovanovich, Stevan B. [11 ]
Krstic, Predrag S. [12 ]
Lindsay, Stuart [13 ,14 ,15 ]
Ling, Xinsheng Sean [16 ]
Mastrangelo, Carlos H. [17 ]
Meller, Amit [18 ]
Oliver, John S. [19 ]
Pershin, Yuriy V. [7 ]
Ramsey, J. Michael [20 ]
Riehn, Robert [21 ]
Soni, Gautam V. [18 ]
Tabard-Cossa, Vincent [3 ]
Wanunu, Meni
Wiggin, Matthew [22 ]
Schloss, Jeffery A. [23 ]
机构
[1] Harvard Univ, Dept Mol & Cell Biol, Cambridge, MA 02138 USA
[2] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA
[3] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V6T 1Z1, Canada
[4] Univ Oxford, Dept Biol Chem, Oxford OX1 3TA, England
[5] Fdn Appl Mol Evolut, Gainesville, FL 32604 USA
[6] Univ Washington, Dept Phys, Seattle, WA 98195 USA
[7] Univ Calif San Diego, Dept Phys, La Jolla, CA 92093 USA
[8] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[9] Elect BioSci, San Diego, CA 92121 USA
[10] Univ Calif San Diego, Dept Bioengn, San Diego, CA 92093 USA
[11] Microchip Biotechnol Inc, Dublin, CA 94568 USA
[12] Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
[13] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA
[14] Arizona State Univ, Dept Chem, Tempe, AZ 85287 USA
[15] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
[16] Brown Univ, Dept Phys, Providence, RI 02912 USA
[17] Case Western Reserve Univ, Cleveland, OH 44106 USA
[18] Boston Univ, Boston, MA 02215 USA
[19] NABsys Inc, Providence, RI 02906 USA
[20] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[21] N Carolina State Univ, Dept Phys, Raleigh, NC 27695 USA
[22] Univ British Columbia, Dept Biochem, Vancouver, BC V6T 1Z3, Canada
[23] Natl Human Genome Res Inst, Natl Inst Hlth, Bethesda, MD 20892 USA
关键词
D O I
10.1038/nbt.1495
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A nanopore-based device provides single-molecule detection and analytical capabilities that are achieved by electrophoretically driving molecules in solution through a nano-scale pore. The nanopore provides a highly confined space within which single nucleic acid polymers can be analyzed at high throughput by one of a variety of means, and the perfect processivity that can be enforced in a narrow pore ensures that the native order of the nucleobases in a polynucleotide is reflected in the sequence of signals that is detected. Kilobase length polymers (single-stranded genomic DNA or RNA) or small molecules (e.g., nucleosides) can be identified and characterized without amplification or labeling, a unique analytical capability that makes inexpensive, rapid DNA sequencing a possibility. Further research and development to overcome current challenges to nanopore identification of each successive nucleotide in a DNA strand offers the prospect of 'third generation' instruments that will sequence a diploid mammalian genome for similar to$1,000 in similar to 24 h.
引用
收藏
页码:1146 / 1153
页数:8
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