TY - JOUR
T1 - Label-free electrical detection of DNA hybridization for the example of influenza virus gene sequences
AU - Kukol, A
AU - Li, P
AU - Estrela, Pedro
AU - Ko-Ferrigno, P
AU - Migliorato, P
N1 - ID number: 000253010100018
PY - 2008
Y1 - 2008
N2 - Microarrays based on DNA-DNA hybridization are potentially useful for detecting and subtyping viruses but require fluorescence labeling and imaging equipment. We investigated a label-free electrical detection system using electrochemical impedance spectroscopy that is able to detect hybridization of DNA target sequences derived from avian H5N1 influenza virus to gold surface-attached single-stranded DNA oligonucleotide probes. A 23-nt probe is able to detect a 120-nt base fragment of the influenza A hemagglutinin gene sequence. We describe a novel method of data analysis that is compatible with automatic measurement without operator input, contrary to curve fitting used in conventional electrochemical impedance spectroscopy (EIS) data analysis. A systematic investigation of the detection signal for various spacer molecules between the oligonucleotide probe and the gold surface revealed that the signal/background ratio improves as the length of the spacer increases, with a 12- to 18-atom spacer element being optimal. The optimal spacer molecule allows a detection limit between 30 and 100 fmol DNA with a macroscopic gold disc electrode of I mm radius. The dependence of the detection signal on the concentration of a 23-nt target follows a binding curve with an approximate 1:1 stoichiometry and a dissociation constant of K-D = 13 +/- 4 nM at 295 K. (c) 2007 Elsevier Inc. All rights reserved.
AB - Microarrays based on DNA-DNA hybridization are potentially useful for detecting and subtyping viruses but require fluorescence labeling and imaging equipment. We investigated a label-free electrical detection system using electrochemical impedance spectroscopy that is able to detect hybridization of DNA target sequences derived from avian H5N1 influenza virus to gold surface-attached single-stranded DNA oligonucleotide probes. A 23-nt probe is able to detect a 120-nt base fragment of the influenza A hemagglutinin gene sequence. We describe a novel method of data analysis that is compatible with automatic measurement without operator input, contrary to curve fitting used in conventional electrochemical impedance spectroscopy (EIS) data analysis. A systematic investigation of the detection signal for various spacer molecules between the oligonucleotide probe and the gold surface revealed that the signal/background ratio improves as the length of the spacer increases, with a 12- to 18-atom spacer element being optimal. The optimal spacer molecule allows a detection limit between 30 and 100 fmol DNA with a macroscopic gold disc electrode of I mm radius. The dependence of the detection signal on the concentration of a 23-nt target follows a binding curve with an approximate 1:1 stoichiometry and a dissociation constant of K-D = 13 +/- 4 nM at 295 K. (c) 2007 Elsevier Inc. All rights reserved.
UR - http://www.scopus.com/inward/record.url?scp=38649107404&partnerID=8YFLogxK
UR - http://dx.doi.org/10.1016/j.ab.2007.10.035
U2 - 10.1016/j.ab.2007.10.035
DO - 10.1016/j.ab.2007.10.035
M3 - Article
SN - 0003-2697
VL - 374
SP - 143
EP - 153
JO - Analytical Biochemistry
JF - Analytical Biochemistry
IS - 1
ER -