TY - JOUR
T1 - 2d lh and 31p nmr spectra and distorted a-dna-like duplex structure of a phosphorodithioate oligonucleotide
AU - Cho, Yesun
AU - Zhu, Frank C.
AU - Luxon, Bruce A.
AU - Gorenstein, David G.
N1 - Funding Information:
Supported by NIH (AI27744), the Purdue University Biochemical Magnetic Resonance Laboratory which is supported by the NIH designated AIDS Research Center at Purdue (AI727713) and the NSF designated Biological Facilities Center on Biomolecular NMR, Structure and Design at Purdue (grants BBS 8614177 and 8714258 from the Division of Biological Instrumentation).
PY - 1993/12
Y1 - 1993/12
N2 - Assignment of the1H and3IP NMR spectra of a phosphorodithioate modified oligonucleotide decamer duplex, d(CGCTTpS2AAGCG)2(10-mer-S; a site of dithioate substitution is designated with the symbols Ps2), was achieved by two-dimensional homonuclearTOCSY, NOESY and1H-31P Pure Absorption phase Constant time (PAC) heteronuclear correlation spectroscopy. In contrast to the parent palindromic decamer sequence (1) which has been shown to exist entirely in the duplex B-DNA conformation under comparable conditions (100 mM KC1), the dithiophosphate analogue forms a hairpin loop. However, the duplex form of the dithioate oligonucleotide can be stabilized at lower temperatures, higher salt and strand concentration. The solution structure of the decamer duplex was calculated by an iterative hybrid relaxation matrix method (MORASS) combined with 2D NOESY-distance restrained molecular dynamics. These backbone modified compounds, potentially attractive antisense oligonucleotide agents, are often assumed to possess similar structure as the parent nucleic acid complex. Importantly, the refined structure of the phosphorodithioate duplex shows a significant deviation from the parent unmodified, phosphoryl duplex. An overall bend and unwinding in the phosphorodithioate duplex is observed. The structural distortion of the phosphorodithioate duplex was confirmed by comparison of helicoidal parameters and groove dimensions. Especially, the helical twists of the phosphorodithioate decamer deviate significantly from the parent phosphoryl decamer. The minor groove width of phosphorodithioate duplex 10- mer-S varies between 8.4 and 13.3 Å which is much wider than those of the parent phosphoryl decamer d(CGCTTAAGCG)2(4.2~9.4 Å). The larger minor groove width of 10-mer-S duplex contributes to the unwinding of the backbone and indicates that the duplex has an overall A- DNA-like conformation in the region surrounding the dithiophosphate modification.
AB - Assignment of the1H and3IP NMR spectra of a phosphorodithioate modified oligonucleotide decamer duplex, d(CGCTTpS2AAGCG)2(10-mer-S; a site of dithioate substitution is designated with the symbols Ps2), was achieved by two-dimensional homonuclearTOCSY, NOESY and1H-31P Pure Absorption phase Constant time (PAC) heteronuclear correlation spectroscopy. In contrast to the parent palindromic decamer sequence (1) which has been shown to exist entirely in the duplex B-DNA conformation under comparable conditions (100 mM KC1), the dithiophosphate analogue forms a hairpin loop. However, the duplex form of the dithioate oligonucleotide can be stabilized at lower temperatures, higher salt and strand concentration. The solution structure of the decamer duplex was calculated by an iterative hybrid relaxation matrix method (MORASS) combined with 2D NOESY-distance restrained molecular dynamics. These backbone modified compounds, potentially attractive antisense oligonucleotide agents, are often assumed to possess similar structure as the parent nucleic acid complex. Importantly, the refined structure of the phosphorodithioate duplex shows a significant deviation from the parent unmodified, phosphoryl duplex. An overall bend and unwinding in the phosphorodithioate duplex is observed. The structural distortion of the phosphorodithioate duplex was confirmed by comparison of helicoidal parameters and groove dimensions. Especially, the helical twists of the phosphorodithioate decamer deviate significantly from the parent phosphoryl decamer. The minor groove width of phosphorodithioate duplex 10- mer-S varies between 8.4 and 13.3 Å which is much wider than those of the parent phosphoryl decamer d(CGCTTAAGCG)2(4.2~9.4 Å). The larger minor groove width of 10-mer-S duplex contributes to the unwinding of the backbone and indicates that the duplex has an overall A- DNA-like conformation in the region surrounding the dithiophosphate modification.
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U2 - 10.1080/07391102.1993.10508023
DO - 10.1080/07391102.1993.10508023
M3 - Article
C2 - 8129879
AN - SCOPUS:0027788136
SN - 0739-1102
VL - 11
SP - 685
EP - 702
JO - Journal of Biomolecular Structure and Dynamics
JF - Journal of Biomolecular Structure and Dynamics
IS - 3
ER -