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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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Published in: | Bioorganic & medicinal chemistry 2007-12, Vol.15 (24), p.7840-7849 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 0968-0896 1464-3391 |
DOI: | 10.1016/j.bmc.2007.08.042 |