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Clinical Chemistry 0: clinchem.2007.091231v1, 2007; 10.1373/clinchem.2007.091231
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Received on April 30, 2007
Accepted on August 30, 2007

Oak Ridge Conference

Progress toward Ultrafast DNA Sequencing Using Solid-State Nanopores

Gautam V. Soni 1 Amit Meller 1*

1 Department of Biomedical Engineering, Boston University, Boston, MA

* To whom correspondence should be addressed. E-mail: ameller{at}bu.edu.

Background: Measurements of the ionic current flowing through nanometer-scale pores (nanopores) have been used to analyze single DNA and RNA molecules, with the ultimate goal of achieving ultrafast DNA sequencing. However, attempts at purely electronic measurements have not achieved the signal contrast required for single nucleotide differentiation. In this report we propose a novel method of optical detection of DNA sequence translocating through a nanopore.

Methods: Each base of the target DNA sequence is 1st mapped onto a 2-unit code, 2 10-bp nucleotide sequence by biochemical conversion into Designed DNA Polymers. These 2-unit codes are then hybridized to complementary, fluorescently labeled, and self-quenching molecular beacons. As the molecular beacons are sequentially unzipped during translocation through a <2-nm-wide nanopore, their fluorescent tags are unquenched and are read by a custom-built dual-color total internal reflection fluorescence (TIRF) microscope. The 2-color optical signal is then correlated to the target DNA sequence.

Results: We successfully performed biochemical conversion of the lambda genome. A dual-color TIRFM with single-molecule resolution was constructed, and controlled fabrication of 1-dimensional and 2-dimensional arrays of solid-state nanopores was performed. Finally, a nanofluidic cell assembly was constructed for TIRF-based optical detection of voltage-driven DNA translocation through a nanopore.

Conclusions: We present a novel nanopore-based DNA sequencing technique that uses an optical readout of DNA translocating through a nanopore. Our technique offers better nucleotide differentiation in sequence readout, as well as the possibility of large-scale parallelism using nanopore arrays.




The following articles in journals at HighWire Press have cited this article:


Home page
Proc. Natl. Acad. Sci. USAHome page
G. Maglia, M. R. Restrepo, E. Mikhailova, and H. Bayley
Enhanced translocation of single DNA molecules through {alpha}-hemolysin nanopores by manipulation of internal charge
PNAS, December 16, 2008; 105(50): 19720 - 19725.
[Abstract] [Full Text] [PDF]




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Copyright © 2007 by the American Association for Clinical Chemistry.