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Application of DNA and RNA Beacons in Electroanalysis: What Are Limits for Sensitivity and Selectivity?
|Elena E. Ferapontova
Interdisciplinary Nanoscience Center, iNANO, Aarhus University, Ny Munkegade 120, Aarhus, Aarhus 8000, Denmark
At iNANO we aim at the development of new electrochemical biosensor technologies for analysis of cancer gene biomarkers, pathogens and small molecules of interest, which is crucial for efficient diagnostics of cancer and infectious diseases, and neurological disorders. We use small, functional DNA and RNA nanoblocks to create molecular assemblies with improved structural and biosensing properties that in combination with electrochemistry approach may provide extremely sensitive and accurate, yet simple, inexpensive and robust gene-based sensing platforms. I will overview the design and our studies of electrochemically-labeled DNA/RNA beacon structures that undergo distinct structural changes at electrodes upon hybridization phenomena (i.e. chemical recognition of one DNA sequence by another) or upon binding of other molecules of interest. In the latter case, we use so-called aptamers, which are nucleic acids designed to selectively bind to certain analyte, from small molecules to proteins and cells. I will discuss the general limits for selectivity and sensitivity of the developed assays.
Presentation: Keynote lecture at SMCBS'2009 International Workshop, by Elena E. Ferapontova
See On-line Journal of SMCBS'2009 International Workshop
Submitted: 2009-08-29 19:06 Revised: 2009-08-29 19:13