From Microarrays to Nanoarrays: Measuring Hybridisation on Single Molecule Probes
Jens Sobek, Research Scientist, University of Zurich
Microarray technology is a story of success for about 20 years now. In an incalculable number
of publications many fascinating applications were reported covering (nearly) all classes of
probes and samples. The disadvantages are also known and apparent, ranging from tedious
spotting, effects of probe surface density, to the difficulties generating kinetic data, to name a
few. Applying a new technology, we are trying to find new ways in order to overcome some of the
limitations intrinsic to microarraying. Using the example of hybridisation of short
oligonucleotides, we are studying the kinetics of molecular interactions of a single probe
molecule immobilised on a chip surface. The chip consists of nanostructures of about 100 nm
diameter which creates a reaction volume in the order of some zeptoliter (10-21 L). Using
160000 of these nanostructures on a chip in parallel, we are aiming for reducing microarray
spots with respect to the number of immobilised molecules from about 10^12 to 1,
and performing experiments with a single molecule per nanostructure.
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