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Oligonucleotides osmium

Fig. 2 Emission spectra of double-stranded DNA molecules composed of an oligonucleotide modified at its 5 -end with ruthenium(II) nucleoside 5 and its complementary strand a without modification, and with a related osmium(II) label at a distance of b 61, c 52, d 43, e 31, f 21 and g 16 A. The Ru-Os distances are based on a helical DNA model [34]... Fig. 2 Emission spectra of double-stranded DNA molecules composed of an oligonucleotide modified at its 5 -end with ruthenium(II) nucleoside 5 and its complementary strand a without modification, and with a related osmium(II) label at a distance of b 61, c 52, d 43, e 31, f 21 and g 16 A. The Ru-Os distances are based on a helical DNA model [34]...
Dorcier A, Dyson PJ, Gossens C, Rothlisberger U, Scopelliti R, Tavemelli I (2005) Binding of organometallic ruthenium(II) and osmium(II) complexes to an oligonucleotide a combined mass spectrometric and theoretical study. Organometallics 24 2114—2123... [Pg.51]

The distortions induced in the DNA double helix by the interstrand cross-links have been characterized by several techniques. As judged by chemical probes (diethyl pyrocarbonate, hydroxylamine, osmium tetroxide), antibodies to cisplatin-modified poly(dG-dC)-poly(dG-dC), natural (DNase I) and artificial (1,10-phenanthroline-copper complex) nucleases, the cytosine residues are accessible to the solvent, and the distortions are located at the level of the adduct [48-50]. From the electrophoretic mobility of the multimers of double-stranded oligonucleotides containing a single interstrand cross-link [50] it is deduced that the DNA double helix is unwound (79°) and its axis is bent (45°). [Pg.161]

Olefin cyclization, 305-307 Olefin isomerization, 242-243 Olefin synthesis, 315—316, 319-320 Oligonucleotides, 19 Osmium-on-carbon, 216 Oxalic acid, 79, 279, 280, 283 Oxalyl chloride, 69, 216-217 l,2-Oxathiolane-2-oxide, 149... [Pg.200]

G.-U. Flechsig and T. Reske, Electrochemical detection of DNA hybridization by means of osmium tetroxide complexes and protective oligonucleotides, Ann/. Chem. 79(5), 2125-2130 (2007). [Pg.327]

When a metal complex is formed with the nucleic acid base of single-stranded DNA (ssDNA), such ssDNA can be used as an alternative electrochemically-active DNA-binding ligand. For example, Palecek and coworkers reported the formation of a reversible redox-active metal complex by the reaction of osmium tetraoxide-pyridine with the thymine (T) base of ssDNA, and they developed an electrochemical gene detection method based on this modified oligonucleotide as a DNA probe [3]. [Pg.305]

Holmberg RC, Tierney MT, Ropp PA, Berg EE, Grinstaff MW, Thorp HH (2003) Intramolecular electrocatalysis of 8-oxo-guanine oxidation secondary structure control of electron transfer in osmium-labeled oligonucleotides. Inorg Chem 42 6379-6387... [Pg.350]


See other pages where Oligonucleotides osmium is mentioned: [Pg.56]    [Pg.213]    [Pg.215]    [Pg.113]    [Pg.265]    [Pg.452]    [Pg.342]    [Pg.174]    [Pg.213]    [Pg.215]    [Pg.187]    [Pg.451]    [Pg.316]    [Pg.317]   
See also in sourсe #XX -- [ Pg.134 ]




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Osmium-modified oligonucleotides

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