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Photomodulation of PS-modified oligonucleotides containing azobenzene substituent at pre-selected positions in phosphate backbone

A new protocol has been developed for incorporation of photoisomerizable azobenzene substituent into synthetic PS-oligonucleotides. A new protocol has been developed for incorporation of a photoisomerizable azobenzene moiety into synthetic stereo-enriched [R p] and [S p] PS-oligonucleotides. The azo...

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Bibliographic Details
Published in:Bioorganic & medicinal chemistry 2007-12, Vol.15 (24), p.7840-7849
Main Authors: Patnaik, Satyakam, Kumar, P., Garg, B.S., Gandhi, R.P., Gupta, K.C.
Format: Article
Language:English
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Summary:A new protocol has been developed for incorporation of photoisomerizable azobenzene substituent into synthetic PS-oligonucleotides. A new protocol has been developed for incorporation of a photoisomerizable azobenzene moiety into synthetic stereo-enriched [R p] and [S p] PS-oligonucleotides. The azobenzene pendant is attached at pre-selected positions in internucleotidic phosphorothioate oligonucleotides of both [R p] and [S p] diastereomers using a novel reagent, N-iodoacetyl- p-aminoazobenzene, 1. The modified oligomers are purified on HPLC, characterized by LC–MS, and examined for their thermal and photoisomerization properties. The azobenzene moiety imparts greater stability to oligomer duplexes in ( E) N N configuration as compared to ( Z) configuration. The placement of the azobenzene pendant close to 5′-terminus ( n − 1) and 3′-terminus of the modified PS-oligos contributes maximum stability to the duplex while a gradual decline in stability occurs with azobenzene moving toward middle of the duplex. Circular Dichroism studies reveal that the chiral environment at the phosphorus center of the PS-oligos does not alter the global conformation of the DNA duplex as such, suggesting conservation of conformation of the modified DNA strands.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2007.08.042