RESUMEN
New oligonucleotide analogues with triazole internucleotide linkages were synthesized, and their hybridization properties were studied. The analogues demonstrated DNA binding affinities similar to those of unmodified oligonucleotides. The modification was shown to protect the oligonucleotides from nuclease hydrolysis. The modified oligonucleotides were tested as PCR primers. Modifications remote from the 3'-terminus were tolerated by polymerases. Our results suggest that these new oligonucleotide analogues are among the most promising triazole DNA mimics characterized to date.
Asunto(s)
ADN/química , Sondas Moleculares/síntesis química , Oligonucleótidos/química , Triazoles/química , Desoxirribonucleasas/química , Hidrólisis , Imitación Molecular , Desnaturalización de Ácido Nucleico , Hibridación de Ácido Nucleico , Reacción en Cadena de la PolimerasaRESUMEN
We report a novel approach for the attachment of DNA fragments to the surface of live cells. By using fluorescence microscopy and flow cytometry we demonstrated that our synthetic conjugates of fatty acid with oligonucleotides can be incorporated in plasma membrane and then hybridized with complementary sequences at the cell surface. Method permits to control amount of immobilized DNA on the cell surface. All procedures can be completed within minutes and do not alter cell viability. Using this approach we tethered floating myeloid HL-60 cells to adherent A431 epitheliocytes in a sequence specific fashion. Thus, this method allows rapid and simple DNA multicoding of the cell surface and, therefore, opens new opportunities in manipulating with cell-cell interactions.
Asunto(s)
Membrana Celular/química , ADN/química , Hibridación de Ácido Nucleico , Oligonucleótidos/química , Adhesión Celular , Línea Celular , Ácidos Grasos/química , Citometría de Flujo , Colorantes Fluorescentes , Células HL-60 , Humanos , Células Jurkat , Microscopía Fluorescente , Oligonucleótidos/análisis , Oligonucleótidos/síntesis químicaRESUMEN
A common problem of the preparation of hexachlorofluorescein labeled oligonucleotides is the transformation of the fluorophore to an arylacridine derivative under standard ammonolysis conditions. We show here that the arylacridine byproduct with distinct optical characteristics cannot be efficiently separated from the major product by HPLC or electrophoretic methods, which hampers precise physicochemical experiments with the labeled oligonucleotides. Studies of the transformation mechanism allowed us to select optimal conditions for avoiding the side reaction. The novel method for the post-synthetic deblocking of hexachlorofluorescein-labeled oligodeoxyribonucleotides described in this paper prevents the formation of the arylacridine derivative, enhances the yield of target oligomers, and allows them to be proper real-time PCR probes.