Bökemeier W, Lezius A G
Nucleic Acids Res. 1986 Mar 11;14(5):2241-9. doi: 10.1093/nar/14.5.2241.
The helical twist of poly d(A-s4T) was determined from the periodicity of the cleavage patterns of the double stranded polydeoxynucleotide adsorbed on calcium phosphate and found to be 14 bp per turn. Both cleavage patterns and 31P NMR spectra indicate a mononucleotide structure rather than an alternating B DNA like poly d(A-T). The failure of nucleosome formation excludes a B type structure. The discrepancy of the mononucleotide structure found in 31P NMR spectra and the dinucleotide structure given by X ray fiber diffraction is explained by an alternating tilt of the planes of the base pairs (base roll) as a consequence of a strong propeller twist. The importance of interstrand stacking interactions of adjacent 4-thiothymidines for the helical stability is discussed.
聚d(A-s4T)的螺旋扭曲是根据吸附在磷酸钙上的双链聚脱氧核苷酸切割模式的周期性确定的,发现每圈为14个碱基对。切割模式和31P NMR光谱均表明是单核苷酸结构,而非类似聚d(A-T)的交替B型DNA。核小体形成的失败排除了B型结构。31P NMR光谱中发现的单核苷酸结构与X射线纤维衍射给出的二核苷酸结构之间的差异,可通过由于强烈的螺旋桨扭曲导致碱基对平面交替倾斜(碱基滚动)来解释。讨论了相邻4-硫代胸苷的链间堆积相互作用对螺旋稳定性的重要性。