TY - JOUR
T1 - Solid-state nanopore channels with DNA selectivity
AU - Iqbal, Samir M.
AU - Akin, Demir
AU - Bashir, Rashid
N1 - Funding Information:
We acknowledge very useful discussions with M.A. Alam, D.E. Bergstrom and G. Balasundaram (Purdue University), P. Kohli (Southern Illinois University, Carbondale), and also C. Martin (University of Florida) for providing critical input to the conceptual discussion. We are thankful to B.M.K. Venkatesan, H. Chang, E.P. Judokusumo, R. Qaseem and P. Bajaj for help in data analysis. We also thank E.J. Basgall at PSU for electron-beam lithography through the NSF-funded National Nanotechnology Infrastructure Network. Partial wafer fabrication was performed in the Nanotechnology Core Facility at University of Illinois at Chicago. This work was initiated with support from NIH/NIBIB Award No. R21RR15118-01, and subsequently supported by the NASA Institute for Nanoelectronics and Computing at Purdue under Award No. NCC 2–1363. Supplementary Information accompanies this paper on www.nature.com/naturenanotechnology. Correspondence and requests for materials should be addressed to R.B.
PY - 2007/4
Y1 - 2007/4
N2 - Solid-state nanopores have emerged as possible candidates for next-generation DNA sequencing devices. In such a device, the DNA sequence would be determined by measuring how the forces on the DNA molecules, and also the ion currents through the nanopore, change as the molecules pass through the nanopore. Unlike their biological counterparts, solid-state nanopores have the advantage that they can withstand a wide range of analyte solutions and environments. Here we report solid-state nanopore channels that are selective towards single-stranded DNA (ssDNA). Nanopores functionalized with a 'probe' of hair-pin loop DNA can, under an applied electrical field, selectively transport short lengths of 'target' ssDNA that are complementary to the probe. Even a single base mismatch between the probe and the target results in longer translocation pulses and a significantly reduced number of translocation events. Our single-molecule measurements allow us to measure separately the molecular flux and the pulse duration, providing a tool to gain fundamental insight into the channel-molecule interactions. The results can be explained in the conceptual framework of diffusive molecular transport with particle-channel interactions.
AB - Solid-state nanopores have emerged as possible candidates for next-generation DNA sequencing devices. In such a device, the DNA sequence would be determined by measuring how the forces on the DNA molecules, and also the ion currents through the nanopore, change as the molecules pass through the nanopore. Unlike their biological counterparts, solid-state nanopores have the advantage that they can withstand a wide range of analyte solutions and environments. Here we report solid-state nanopore channels that are selective towards single-stranded DNA (ssDNA). Nanopores functionalized with a 'probe' of hair-pin loop DNA can, under an applied electrical field, selectively transport short lengths of 'target' ssDNA that are complementary to the probe. Even a single base mismatch between the probe and the target results in longer translocation pulses and a significantly reduced number of translocation events. Our single-molecule measurements allow us to measure separately the molecular flux and the pulse duration, providing a tool to gain fundamental insight into the channel-molecule interactions. The results can be explained in the conceptual framework of diffusive molecular transport with particle-channel interactions.
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U2 - 10.1038/nnano.2007.78
DO - 10.1038/nnano.2007.78
M3 - Article
C2 - 18654270
AN - SCOPUS:34248399955
SN - 1748-3387
VL - 2
SP - 243
EP - 248
JO - Nature Nanotechnology
JF - Nature Nanotechnology
IS - 4
ER -