A simple and rapid procedure whereby human genomic DNA can be purified
in a PCR amplifiable form from whole blood is described. In a first s
tep, human genomic DNA is hybridized in solution to a biotinylated pep
tide nucleic acid (PNA), which forms a high-affinity triplex with A(7)
sequence motifs in the target DNA. The complex is then captured onto
paramagnetic streptavidin-coated particles, which are subsequently tra
nsferred directly into the PCR. The purification method effectively re
moves inhibitors of the PCR from as much as 500 mu L of whole blood.