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Electrical detection of the biological interaction of a charged peptide via gallium arsenide junction-field-effect transistors

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7 Author(s)
Kangho Lee ; School of Electrical and Computer Engineering, The Institute for Nanoelectronics and Computing, and Birck Nanotechnology Center, Purdue University, West Lafayette, Indiana 47907, USA ; Nair, P.R. ; Alam, M.A. ; Janes, D.B.
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GaAs junction-field-effect transistors (JFETs) are utilized to achieve label-free detection of biological interaction between a probe transactivating transcriptional activator (TAT) peptide and the target trans-activation-responsive (TAR) RNA. The TAT peptide is a short sequence derived from the human immunodeficiency virus-type 1 TAT protein. The GaAs JFETs are modified with a mixed adlayer of 1-octadecanethiol (ODT) and TAT peptide, with the ODT passivating the GaAs surface from polar ions in physiological solutions and the TAT peptide providing selective binding sites for TAR RNA. The devices modified with the mixed adlayer exhibit a negative pinch-off voltage (VP) shift, which is attributed to the fixed positive charges from the arginine-rich regions in the TAT peptide. Immersing the modified devices into a TAR RNA solution results in a large positive VP shift (≫1 V) and a steeper subthreshold slope (∼80 mV/decade), whereas “dummy” RNA induced a small positive VP shift (∼0.3 V) without a significant change in subthreshold slopes (∼330 mV/decade). The observed modulation of device characteristics is analyzed with analytical modeling and two-dimensional numerical device simulations to investigate the electronic interactions between the GaAs JFETs and biological molecules.

Published in:

Journal of Applied Physics  (Volume:103 ,  Issue: 11 )

Date of Publication:

Jun 2008

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