Abstract
Poly(dA).poly(dT), but not B-form DNA, is specifically recognized by experimentally induced anti-kinetoplast or anti-poly(dA).poly(dT) immunoglobulins. Antibody binding is completely competed by poly(dA).poly(dT) and poly(dA).poly(dU) but not by other single- or double-stranded DNA sequences in a right-handed B-form. Antibody interaction with poly(dA).poly(dT) depends on immunoglobulin concentration, incubation time and temperature, and is sensitive to elevated ionic strengths. Similar conformations, for example, (dA)4-6 X (dT)4-6, in the kinetoplast DNA of the parasite Leishmania tarentolae are also immunogenic and induce specific anti-poly(dA).poly(dT) antibodies. These antibody probes specifically recognize nuclear and kinetoplast DNA in fixed flagellated kinetoplastid cells as evidenced by immunofluorescence microscopy. Anti-poly(dA).poly(dT) immunofluorescence is DNase-sensitive and competed by poly(dA).poly(dT), but not other classical double-stranded B-DNAs. Thus, these unique cellular B'-DNA helices are immunogenic and structurally similar to synthetic poly(dA).poly(dT) helices in solution.
MeSH Terms
Animals
Antibody Specificity
Female
Immunoglobulins/immunology
Nucleic Acid Conformation
Poly dA-dT/immunology
Polydeoxyribonucleotides/immunology
Rabbits
Sodium Chloride/pharmacology
Chemicals
Immunoglobulins
Polydeoxyribonucleotides
Poly dA-dT
Sodium Chloride
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Diekmann S
Zarling D A
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