Optical detection of DNA translocation through silicon nanopore by ultraviolet light
Source abstract
Abstract
In this paper, we propose a new optical detection scheme for nanopore-based DNA sequencing with high resolution towards eventual base identification. We use ultraviolet light for excitation of a fluorescent probe attached to DNA and a nanopore in the silicon membrane that has a significantly large refractive index and an extinction coefficient at ultraviolet wavelengths. In this study, numerical electromagnetic simulation revealed that the z-polarization component (perpendicular to the membrane plane) of the electric field was dominant near the nanopore and generated a large electric field gradient at the nanopore exit, typically with a decay length of 2 nm for a nanopore with diameter of 7 nm. The large extinction coefficient contributed to reduction in background noise coming from fluorophore-labeled DNA strands that remain behind the membrane (the cis side of the membrane). We observed a high signal-to-noise ratio of single DNA translocation events under the application of an electric field.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nanopore and Nanochannel Transport Studies · Microfluidic and Bio-sensing Technologies · Microfluidic and Capillary Electrophoresis Applications
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References (15)
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1. C. Dekker, Nat. Nanotechnol. 2, 209 (2007)10.1038/nnano.2007.27 ↗
2. B.M. Venkatesan, R. Bashir, Nat. Nanotechnol. 6, 615 (2011)10.1038/nnano.2011.129 ↗
3. J. Clarke, H.C. Wu, L. Jayasinghe, A. Patel, S. Reid, H. Bayley, Nat. Nanotechnol. 4, 265 (2009)10.1038/nnano.2009.12 ↗
4. S. Benner, R. Chen, A. Wilson, R. Shumays, N. Hurt, K. Lieberman, D.W. Deamer, W.B. Dunbar, M. Akenson, ACS Nano 3, 1457 (2009)10.1021/nn900303g ↗
5. M. Tsutsui, M. Taniguchi, K. Yokota, T. Kawai, Nat. Nanotechnol. 5, 286 (2010)10.1038/nnano.2010.42 ↗
6. Q. Zhao, G. Sigalov, V. Dimitrov, B. Dorvel, U. Mirsaidov, S. Sligar, A. Aksimentiev, G. Timp, Nano Lett. 7, 1680 (2007)10.1021/nl070668c ↗
7. S.M. Bezrukov, I. Vodyanoy, V.A. Parsegian, Nature 370, 279 (1993)10.1038/370279a0 ↗
8. A.J. Storm, J.H. Chen, X.S. Ling, H.W. Zandbergen, C. Dekker, Nat. Mater. 2, 537 (2003)10.1038/nmat941 ↗
9. G.A.T. Chansin, R. Mulero, J. Hong, M.J. Kim, A. Andrew, J. deMello, J. Edel, Nano Lett. 7, 2901 (2007)10.1021/nl071855d ↗
10. J. Li, M. Gershow, D. Stein, E. Brandin, J.A. Golovchenko, Nat. Mater. 2, 611 (2003)10.1038/nmat965 ↗
11. B. McNally, A. Singer, Z. Yu, Y. Sun, Z. Weng, A. Meller, Nano Lett. 10, 2237 (2010)10.1021/nl1012147 ↗
12. B. Sick, B. Hecht, U.P. Wild, L. Novotny, J. Microsc. 202, 365 (2001)10.1046/j.1365-2818.2001.00795.x ↗
13. J. Hong, Y. Lee, G. Chansin, J. Edel, A. deMello, Nanotechnology 19, 165205 (2008)
14. M. Wanunu, J. Sutin, B. McNally, A. Chow, A. Meller, Biophys. J. 95, 4716 (2008)10.1529/biophysj.108.140475 ↗
15. M. Wanunu, W. Morrison, Y. Rabin, A.Y. Grosberg, A. Meller, Nat. Nanotechnol. 5, 160 (2010)10.1038/nnano.2009.379 ↗