K-ras Mutation Detection by Hybridization to a Polypyrrole DNA Chip

Background: Detection of mutations in cancer-related genes is of major importance for both basic knowledge and clinical practice. Several strategies have been developed to diagnose these alterations. We describe a method based on polypyrrole DNA chip technology to detect K-ras gene mutations in tumors. Methods: An oligodeoxynucleotide array was constructed on a silicon device by copolymerization of 5*-pyrrole-labeled oligodeoxynucleotides and pyrrole. The samples to be analyzed were then amplified by PCR, and the single-stranded biotin-labeled amplified DNA was specifically hybridized to the addressed probes. Perfectly matched duplexes were detected by fluorescence microscopy using R-phycoerythrin as the detection label. The developed methodology was applied to genotype assignment of K-ras in human samples. The genotypes of 75 DNA genomic samples from colorectal cancer patients were analyzed side by side using direct DNA sequencing and a polypyrrole DNA chip. Results: The chip method unequivocally defined all of the genotypes. Mutations present at <10% of the wildtype DNA concentration could be distinguished. Conclusions: This probe array assay is a rapid and reliable procedure that may be used to detect mutations. © 2001 American Association for Clinical Chemistry