Nucleic Acids Research, 2002, Vol. 30, No. 2 e3
© 2002 Oxford University Press
Genetic screening using the colour change of a PNADNA hybrid-binding cyanine dye
Department of Physical Chemistry, Chalmers University of Technology, S-412 96 Gothenburg, Sweden and 1Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA
As the relationship between human genes and various malfunctions and diseases becomes revealed at an ever-increasing pace, the need arises for the development of rapid genetic screening methods for diagnostic purposes. Genetic diseases show great diversity. Some are caused by a few characteristic localised mutations, while others arise from a large number of variations. Hence, it is unlikely that a single, general diagnostic method that applies to all cases will ever exist. Instead, a combination of methods is frequently applied. Here we propose the use of a dramatic colour change that a cyanine dye, 3,3'-diethylthiadicarbocyanine, displays upon binding to DNAPNA duplexes. This method could become an inexpensive, fast and simple genetic screening test by visual inspection, with no need for complicated equipment. Our results demonstrate that this diagnostic method may be sufficiently sensitive to discriminate between even a fully complementary and a single mutation DNA sequence.
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