TY - JOUR
T1 - A competitor-switched electrochemical sensor for detection of DNA
AU - Fan, Hao
AU - Xing, Rong
AU - Xu, Ying
AU - Chen, Miao
AU - Wang, Qingjiang
AU - He, Pingang
AU - Fang, Yuzhi
PY - 2010/10
Y1 - 2010/10
N2 - A competitor-switched electrochemical sensor based on a generic displacement strategy was designed for DNA detection. In this strategy, an unmodified single-stranded DNA (cDNA) completely complementary to the target DNA served as the molecular recognition element, while a hairpin DNA (hDNA) labeled with a ferrocene (Fc) and a thiol group at its terminals served as both the competitor element and the probe. This electrochemical sensor was fabricated by self-assembling a dsDNA onto a gold electrode surface. The dsDNA was pre-formed through the hybridization of Fc-labeled hDNA and cDNA with their part complementary sequences. Initially, the labeled ferrocene in the dsDNA was far from surface of the electrode, the electrochemical sensor exhibited a "switch-off" mode due to unfavorable electron transfer of Fc label. However, in the presence of target DNA, cDNA was released from hDNA by target DNA, the hairpin-open hDNA restored its original hairpin structure and the ferrocene approached onto the electrode surface, thus the electrochemical sensor exhibited a "switch-on" mode accompanying with a change in the current response. The experimental results showed that as low as 4.4×10-10 mol/L target DNA could be distinguishingly detected, and this method had obvious advantages such as facile operation, low cost and reagentless procedure.
AB - A competitor-switched electrochemical sensor based on a generic displacement strategy was designed for DNA detection. In this strategy, an unmodified single-stranded DNA (cDNA) completely complementary to the target DNA served as the molecular recognition element, while a hairpin DNA (hDNA) labeled with a ferrocene (Fc) and a thiol group at its terminals served as both the competitor element and the probe. This electrochemical sensor was fabricated by self-assembling a dsDNA onto a gold electrode surface. The dsDNA was pre-formed through the hybridization of Fc-labeled hDNA and cDNA with their part complementary sequences. Initially, the labeled ferrocene in the dsDNA was far from surface of the electrode, the electrochemical sensor exhibited a "switch-off" mode due to unfavorable electron transfer of Fc label. However, in the presence of target DNA, cDNA was released from hDNA by target DNA, the hairpin-open hDNA restored its original hairpin structure and the ferrocene approached onto the electrode surface, thus the electrochemical sensor exhibited a "switch-on" mode accompanying with a change in the current response. The experimental results showed that as low as 4.4×10-10 mol/L target DNA could be distinguishingly detected, and this method had obvious advantages such as facile operation, low cost and reagentless procedure.
KW - Biosensors
KW - DNA
KW - Displacement
KW - Switch
UR - https://www.scopus.com/pages/publications/78349273140
U2 - 10.1002/cjoc.201090330
DO - 10.1002/cjoc.201090330
M3 - 文章
AN - SCOPUS:78349273140
SN - 1001-604X
VL - 28
SP - 1978
EP - 1982
JO - Chinese Journal of Chemistry
JF - Chinese Journal of Chemistry
IS - 10
ER -