A FILTER BINDING ASSAY FOR CHARACTERIZATION OF ANTIBODIES TOWARDS DAMAGED DNA

A nitrocellulose filter binding assay was used to characterize rabbit antibodies specific for UV-irradiated DNA. The dissociation constant for the UV-DNA-antibody complex was found to be 4.2 × 10⁻¹² M. No significant binding to unirradiated DNA was observed. Unlabelled single-stranded and double-stranded DNA competed with equal efficiency for the radioactively labelled antigen (UV-irradiated φX174 DNA). The antibodies also bound to OsO₄-treated DNA, suggesting that these polyclonal antibodies also recognize minor photoproducts. Caffeine efficiently decreased binding of the antibodies to UV-irradiated DNA.     

CHARACTERIZATION OF ANTIBODIES SPECIFIC FOR UV-DAMAGED DNA BY ELISA

Abstract— The specificity of affinity purified antibodies raised against UV-irradiated DNA was examined using an enzyme-linked immunosorbent assay. DNA irradiated with UV doses higher than needed for saturation with pyrimidine dimers bound increasing amounts of antibody. Photosensitized DNA, containing high amounts of pyrimidine dimers, showed very poor binding of antibody. When UV-irradiated DNA was given a second dose of 340-nm UV light, the binding of antibodies was abrogated. Taken together, this indicates a major specificity for (6-4)-photoproducts, which are photochemically reversed by UV light in the 340-nm region. The antibodies also showed little but detectable binding to pyrimidine glycols produced in DNA by oxidation with O_sO₄. Previously, we have used these antibodies for the detection of UV-induced DNA damage and its repair in human skin in vivo. These findings indicate that (6-4)-photoproducts, considered highly mutagenic, are repaired in human skin.