Article

An Electrochemical DNA Biosensor Based on Gold Nanofilm and Stable Y Junction Structure

  • Dong Xiaoya ,
  • Zhao Weiwei ,
  • Sun Guobao ,
  • Xu Jingjuan ,
  • Chen Hongyuan
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  • a State Key Lab of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093;
    b Key Laboratory of Modern Agriculture Equipment and Technology, Jiangsu University, Zhenjiang 212013

Received date: 2012-04-11

  Online published: 2012-05-03

Supported by

Project supported by 973 Program (No. 2012CB932600), the National Natural Science Foundation of China (Nos. 21025522, 21135003) and the National Natural Science Foundation of China for Creative Research Groups (No. 21121091).

Abstract

On the basis of gold nanofilm (GNF) electrode and Y junction structure of DNA, a simple and facile single-step DNA sensing protocol with improved sensitivity and lower detection limit was successfully developed. The GNF was prepared via rapid electrooxidization of the gold surface followed by the chemical reduction of the produced gold oxide layer. The capture probe DNA (c-DNA) was firstly immobilized onto GNF electrodes via Au—S bonding, for the subsequent forming of Y junction structure with target DNA (t-DNA) and reporter probe DNA (r-DNA) labeled with methylene blue (MB). Harnessing the unique properties of GNF would allow the improved contact of MB with the electrode surface and hence boost the interfacial electron communication. Experimental results of differential pulse voltammetry (DPV) showed that the peak current of the prepared biosensor was linear with the target DNA concentration from 1.0×10-12 to 1.0×10-9 mol/L and the proposed strategy could detect the target DNA down to the level of 2.4×10-13 mol/L. Comparing with the traditional electrochemical sensors, the present protocol enabled the generation of electrochemical signal from scratch and possessed an improved selectivity against even a single base mismatch. Besides, this DNA sensor exhibited fairly good reproducibility, stability and reusability.

Cite this article

Dong Xiaoya , Zhao Weiwei , Sun Guobao , Xu Jingjuan , Chen Hongyuan . An Electrochemical DNA Biosensor Based on Gold Nanofilm and Stable Y Junction Structure[J]. Acta Chimica Sinica, 2012 , 70(13) : 1457 -1463 . DOI: 10.6023/A12040106

References

[1] Heller, M. J. Annu. Rev. Biomed. Eng. 2002, 4, 129.
[2] Taton, T. A.; Mirkin, C. A.; Letsinger, R. L. Science 2000, 289,1757.
[3] Boon, E. M.; Ceres, D. M.; Drummond, T. G.; Hill, M. G.; Barton,J. K. Nat. Biotechnol. 2000, 18, 1096.
[4] Shan, Y.; Xu, J. J.; Chen, H. Y. Chem. Commun. 2009, 905
[5] Fan, C. H.; Plaxco, K. W.; Heeger, A. J. Trends Biotechnol. 2005,23, 186.
[6] Chen, Z. P.; Peng, Z. F.; Luo, Y.; Qu, B.; Jiang, J. H.; Zhang, X. B.;Shen, G. L.; Yu, R. Q. Biosens. Bioelectron. 2007, 23, 485.
[7] Park, S. J.; Taton, T. A.; Mirkin, C. A. Science 2002, 295, 1503.
[8] Tombelli, S.; Mascini, R.; Braccini, L.; Anichini, M.; Turner, A. P.F. Biosens. Bioelectron. 2000, 15, 363.
[9] Ye, M.; Zhang, Y. Y.; Li, H. T.; Zhang, Y. Q.; Tan, P.; Tang, H.;Yao, S. Z. Biosens. Bioelectron. 2009, 24, 2339.
[10] Hu, K. C.; Lan, D. X.; Li, X. M.; Zhang, S. S. Anal. Chem. 2008, 80,9124.
[11] Loaiza, O. A.; Campuzano, S.; Pedrero, M.; Pividori, M. I.; Garcia,P.; Pingarron, J. M. Anal. Chem. 2008, 80, 8239.
[12] Miranda-Castro, R.; De-Los-Santos-Alvarez, P.; Lobo-Castanon, M.J.; Miranda-Ordieres, A. J.; Tunon-Blanco, P. Anal. Chem. 2007, 79,4050.
[13] Ting, B. P.; Zhang, J.; Gao, Z. Q.; Ying, J. Y. Biosens. Bioelectron.2009, 25, 282.
[14] Wang, J.; Liu, G. D.; Jan, M. R. J. Am. Chem. Soc. 2004, 126, 3010.
[15] Chen, S. T.; Zhang, X. L.; Zhang, Q. H.; Tan, W. H. Nanoscale Res.Lett. 2009, 4, 1159.
[16] Dong, X. Y.; Mi, X. N.; Wang, B.; Xu, J. J.; Chen, H. Y. Talanta2011, 84, 531.
[17] Dong, X. Y.; Mi, X. N.; Zhao, W. W.; Xu, J. J.; Chen, H. Y. Biosens.Bioelectron. 2011, 26, 3654.
[18] Li, D.; Song, S. P.; Fan, C. H. Acc. Chem. Res. 2010, 43, 631.
[19] Lubin, A. A.; Plaxco, K. W. Acc. Chem. Res. 2010, 43, 496.
[20] Uzawa, T.; Cheng, R. R.; White, R. J.; Makarov, D. E.; Plaxco, K.W. J. Am. Chem. Soc. 2010, 132, 16120.
[21] Farjami, E.; Clima, L.; Gothelf, K.; Ferapontova, E. E. Anal. Chem.2011, 83, 1594.
[22] Lubin, A. A.; Lai, R. Y.; Baker, B. R.; Heeger, A. J.; Plaxco, K. W.Anal. Chem. 2006, 78, 5671.
[23] Kang, D.; Zuo, X. L.; Yang, R. Q.; Xia, F.; Plaxco, K. W.; White, R. J. Anal. Chem. 2009, 81, 9109.
[24] Xiao, Y.; Lubin, A. A.; Heeger, A. J.; Plaxco, K. W. Angew. Chem.,Int. Ed. 2005, 44, 5456.
[25] Ricci, F.; Lai, R. Y.; Plaxco, K. W. Chem. Commun. 2007, 3768.
[26] Immoos, C. E.; Lee, S. J.; Grinstaff, M. W. Chem. Biochem. 2004, 5,1100.
[27] Liu, Y.; Tuleouva, N.; Ramanculov, E.; Revzin, A. Anal. Chem.2010, 82, 8131.
[28] Fan, C. H.; Plaxco, K. W.; Heeger, A. J. Proc. Natl. Acad. Sci. U. S.A. 2003, 100, 9134.
[29] Lai, R. Y.; Plaxco, K. W.; Heeger, A. J. Anal. Chem. 2007, 79, 229.
[30] Xiao, Y.; Qu, X. G.; Plaxco, K. W.; Heeger, A. J. J. Am. Chem. Soc.2007, 129, 11896.
[31] Cash, K. J.; Heeger, A. J.; Plaxco, K. W.; Xiao, Y. Anal. Chem.2009, 81, 656.
[32] Immoos, C. E.; Le, S. J.; Grinstaff, M. W. J. Am. Chem. Soc. 2004,126, 10814.
[33] Zhang, Y. L.; Wang, Y.; Wang, H. B.; Jiang, J. H.; Shen, G. L.; Yu,R. Q.; Li, J. H. Anal. Chem. 2009, 81, 1982.
[34] Jin, Y.; Yao, X.; Liu, Q.; Li, J. H. Biosens. Bioelectron. 2007, 22,1126.
[35] Zhao, W.; Xu, J. J.; Shi, C. G.; Chen, H. Y. Electrochem. Commun.2006, 8, 773.
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