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| Physics Colloquium,
September 25, 2007
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Better living through biosensors
Kevin W. Plaxco
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University of California, Santa Barbara
The ideal sensor will be sensitive, specific, versatile, small
enough to hold in your hand, and selective enough to work even when faced
with complex, contaminant-ridden samples. Given the affinity, specificity
and generalizability of biomolecular recognition, biosensors have been
widely touted for their potential to meet these challenging goals. To date,
however, the translation of protein- and DNA-binding events into convenient,
highly selective sensing platforms has proven problematic. We have solved
this problem by employing the ligand-induced folding of proteins, peptides
and DNA as a robust signal transduction mechanism. Our folding-based
sensors are rapid (minutes to seconds), sensitive (micromolar to
femtomolar), fully electronic, and generalizable to an enormous range of
protein, nucleic acid and small molecule targets. The sensors are also
reagentless, greater than 99% reusable, and selective enough to be employed
in (and re-used from) blood, soil and other grossly contaminated materials.
Because of their sensitivity, background suppression, operational
convenience and impressive scalability folding-based biosensors appear
ideally suited for electronic, on-chip applications in pathogen detection,
proteomics and genomics.
Dr. Plaxco's Talk
Dr. Plaxco's Web Site
4:00 p.m., Physics Research Building (PRB), Room 1080
Reception at 3:45 p.m., Atrium, PRB
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