Thomas G A, Peticolas W L
Biopolymers. 1989 Sep;28(9):1625-36. doi: 10.1002/bip.360280911.
A thermally induced left- to right-handed helical interconversion for the self-complementary tetradeoxynucleotide d(CGCG) has been observed in the presence of NaCl at concentrations from 1.5 to 2.25M. Analysis of the Raman spectrum of d(CGCG) in aqueous solution as a function of temperature indicates that at low temperature a left-handed Z-helical form is the predominant species. An increase in temperature results in a decrease in the population of the left-handed form and an increase in the population of the right-handed form. Further elevation in temperature results in extensive disruption of base stacking and a loss of secondary structure. This unstacking presumably represents dissociation to a single-stranded structure. The data suggest that a temperature-dependent Z to B to single-strand transition occurs under the conditions employed. A direct Z to single-strand conversion was not identified. In contrast to previous examples, the thermally induced left- to right-handed helical conversion for d(CGCG) can occur in the absence of chemically modified nucleic acid bases, alcohol solutions, or divalent ions.
在浓度为1.5至2.25M的NaCl存在下,已观察到自互补四脱氧核苷酸d(CGCG)发生热诱导的从左手螺旋到右手螺旋的相互转换。对水溶液中d(CGCG)的拉曼光谱随温度变化的分析表明,在低温下,左手Z螺旋形式是主要物种。温度升高导致左手形式的数量减少,右手形式的数量增加。进一步升高温度会导致碱基堆积广泛破坏和二级结构丧失。这种解堆积大概代表解离为单链结构。数据表明在所采用的条件下发生了温度依赖性的Z到B再到单链的转变。未发现直接的Z到单链的转换。与先前的例子相反,d(CGCG)的热诱导左手到右手螺旋转换可以在没有化学修饰的核酸碱基、醇溶液或二价离子的情况下发生。