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The synthesis of oligodeoxynucleotides d(AT)5 in which specific adenines are linked at C-8 position with dansyl fluorophores via a variable polymethylene spacer chain are reported. This was achieved by a strategy involving prelabelling at the monomeric stage followed by solid phase assembly of oligonucleotides to obtain regiospecifically labeled oligonucleotides. Several mono and polydansyl d(AT)5 derivatives in which the fluorophore is linked via ethylene, tetramethylene and hexamethylene spacer arms were synthesised for a systematic study of their fluorescence characteristics. It was observed that (i) enhancements in fluorescence intensity and emission quantum yields are seen due to multiple labelling, (ii) the magnitude of enhancements are related to labelling configuration and (iii) quenching efficiency is minimal with shorter and rigid spacer arms. The results may aid rational design of multiple fluorescent DNA probes for nonradioactive detection of nucleic acids.

nucleic acids research

Oligonucleotides, part 5+: synthesis and fluorescence studies of DNA oligomers d(AT)<sub>5</sub>containing adenines covalently linked at C-8 with dansyl fluorophore

Oligonucleotides, part 5+: synthesis and fluorescence studies of DNA oligomers d(AT)5containing adenines covalently linked at C-8 with dansyl fluorophore

Oligonucleotides, part 5+: synthesis and fluorescence studies of DNA oligomers d(AT)₅containing adenines covalently linked at C-8 with dansyl fluorophore