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Multiplexed Electrical Detection of Single Viruses

Published online by Cambridge University Press:  01 February 2011

Gengfeng Zheng
Affiliation:
Department of Chemistry and Chemical Biology, Division of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138
Fernando Patolsky
Affiliation:
Department of Chemistry and Chemical Biology, Division of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138
Charles M. Lieber
Affiliation:
Department of Chemistry and Chemical Biology, Division of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138
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Abstract

We report direct, real-time electrical detection of single virus particles with high selectivity using nanowire field effect transistors. Measurements made with nanowire arrays modified with antibodies for influenza A showed discrete conductance changes characteristic of binding and unbinding in the presence of influenza A but not paramyxovirus or adenovirus. Moreover, simultaneous electrical and optical measurements using fluorescently-labelled influenza A demonstrate conclusively that the conductance changes correspond to binding/unbinding of single viruses at the surface of nanowire devices. In addition, studies of nanowire devices modified with antibodies specific for either influenza or adenovirus show that multiple viruses can be selectively detected in parallel. The possibility of large scale integration of these nanowire devices suggests potential for simultaneous detection of a large number of distinct viral threats at the single virus level.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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References

REFERENCES

1. Strauss, E., Strauss, J., Strauss, E. G., Viruses and Human Disease (Academic Press, San Diego, 2001).Google Scholar
2. Storch, G. A., Essential of Diagnostic Virology (Churchill Livingstone, Edinburgh, 1999).Google Scholar
3. Cui, Y., Wei, Q., Park, H., Lieber, C. M., Science 293, 1289 (2001).Google Scholar
4. Hahm, J., Lieber, C. M., Nano Lett. 4, 51 (2004).Google Scholar
5. Chen, R. J. et al., Proc. Natl. Acad. Sci. 100, 4984 (2003).Google Scholar
6. Chen, R. J. et al., J. Am. Chem. Soc. 126, 1563 (2004).Google Scholar
7. Cui, Y., Zhong, Z., Wang, D., Wang, W. U., Lieber, C. M., Nano Lett. 3, 149 (2003).Google Scholar
8. Jin, S. et al., Nano Lett. 4, 915 (2004).Google Scholar
9. Monoclonal anti-hemagglutinin for influenza A was added to a standard virus solution (100 virusesμL) such that the final antibody concentration was 10 μg/ml. The solution was used directly in experiments. Lower antibody concentrations produced partial blockage of the nanowire detector response.Google Scholar
10. Steinfeld, J. I., Francisco, J. S., Hase, W. L., Chemical Kinetics and Dynamics (Prentice Hall, New Jersey, 1998).Google Scholar
11. Herzer, S., Beckett, P., Wegman, T., Moore, P., Life Science News 13, 16 (2003).Google Scholar