PHOSPHOROTHIOATE-MODIFIED OLIGODEOXYRIBONUCLEOTIDES .3. NMR AND UV SPECTROSCOPIC STUDIES OF THE RP-RP, SP-SP, AND RP-SP DUPLEXES, [D(GGSAATTCC)]2, DERIVED FROM DIASTEREOMERIC O-ETHYL PHOSPHOROTHIOATES
PHOSPHOROTHIOATE-MODIFIED OLIGODEOXYRIBONUCLEOTIDES .3. NMR AND UV SPECTROSCOPIC STUDIES OF THE RP-RP, SP-SP, AND RP-SP DUPLEXES, [D(GGSAATTCC)]2, DERIVED FROM DIASTEREOMERIC O-ETHYL PHOSPHOROTHIOATES
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DOI:
10.1093/nar/14.22.9081
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发表时间:
1986-11-25
影响因子:
14.9
通讯作者:
ZON, G
中科院分区:
文献类型:
--
作者:
LAPLANCHE, LA;JAMES, TL;ZON, G
2D—NOE and1H NMR chemical shift data obtained for the title oligonucleotides were compared with similar data previously reported [Broido et al. (1985) Hun J. Biochem. 150, 117–128] for the unmodified “parent”structure, [d(GGAAflCC)]2. The spectroscopically detectable structural perturbations caused by replacement of phosphate oxygen with sulfur were mostly localized within the GsA moiety, and re greater for the Rpconfiguration wherein sulfur is oriented into the major groove of the B—helix. UV—derived Tmmeasurements gave the following order of stability for the duplexes in 0.4 M NaC1: unmodified (33.9±0.1 °C) sp-sp(34.1 °C) > (31.7 °C). The title compounds were prepared by a new and convenient synthetic route which utilized HPLC to separate the diastereomeric O—ethyl phosphorothioate precursors, (Rp)— and (Sp)—d[GG(S, EtMflCC), for subsequent de—ethylation by ammonia in water.