Direct current electrical characterization of ds-DNA in nanogap junctions
Author(s) -
Samir M. Iqbal,
Ganesan Balasundaram,
Subhasis Ghosh,
Donald E. Bergstrom,
Rashid Bashir
Publication year - 2005
Publication title -
applied physics letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 442
eISSN - 1077-3118
pISSN - 0003-6951
DOI - 10.1063/1.1900315
Subject(s) - electromigration , materials science , conductance , molecular electronics , molecule , electrical resistance and conductance , electrode , nanotechnology , electrical resistivity and conductivity , nucleobase , covalent bond , dna , guanine , chemical physics , chemistry , nucleotide , condensed matter physics , composite material , physics , engineering , electrical engineering , biochemistry , organic chemistry , gene
Measurements of DNA conductivity, hybridization, and melting using electronic means can have wide applications in molecular electronics and biological sensors. We have fabricated nanogap break-junctions by electromigration through thin gold-on-titanium films. 18-mer thiolated ds-DNA molecules were covalently attached between the electrodes and dc electrical measurements were done. The conductance was measured through the molecule before and after a temperature ramp from 300 to 400 K. A dramatic decrease in conductance was observed, analogous to an electrical fuse, possibly attributed to complete or partial denaturing of the ds-DNA molecules bridging the nanogaps. We also show evidence that the dc resistance of dry DNA strands of the same length decreases with increasing guanine-cytosine content in the sequence with values ranging from 10 M Ω to 2 G Ω. These findings can have important consequences in DNA-based molecular electronics and direct label-free detection of DNA hybridization.
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