Sequence Specific Detection of Restriction Enzymes at DNA-Modified Carbon Nanotube Field Effect Transistors

Protein–DNA interactions play a central role in many cellular processes, and their misregulation has been implicated in a number of human diseases. Thus, there is a pressing need for the development of analytical strategies for interrogating the binding of proteins to DNA. Herein, we report the elec...

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Veröffentlicht in:Analytical chemistry (Washington) 2014-09, Vol.86 (17), p.8628-8633
Hauptverfasser: Ordinario, David D., Burke, Anthony M., Phan, Long, Jocson, Jonah-Micah, Wang, Hanfei, Dickson, Mary N., Gorodetsky, Alon A.
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Sprache:eng
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Zusammenfassung:Protein–DNA interactions play a central role in many cellular processes, and their misregulation has been implicated in a number of human diseases. Thus, there is a pressing need for the development of analytical strategies for interrogating the binding of proteins to DNA. Herein, we report the electrical monitoring of a prototypical DNA-binding protein, the PvuII restriction enzyme, at microfluidic-encapsulated, DNA-modified carbon nanotube field effect transistors. Our integrated platform enables the sensitive, sequence specific detection of PvuII at concentrations as low as 0.5 pM in a volume of 0.025 μL (corresponding to ∼7500 proteins). These figures of merit compare favorably to state of the art values reported for alternative fluorescent and electrical assays. The overall detection strategy represents a step toward the massively parallel electrical monitoring, identification, and quantification of protein–DNA interactions at arrayed nanoscale devices.
ISSN:0003-2700
1520-6882
DOI:10.1021/ac501441d