Gruenwedel D W, Cruikshank M K
Department of Food Science and Technology, University of California, Davis 95616.
J Inorg Biochem. 1991 Jul;43(1):29-36. doi: 10.1016/0162-0134(91)84066-i.
The conformation of poly[d(T-G).d(C-A)] in aqueous solution (0.1 M NaClO4, 5 mM cacodylic acid buffer, pH 6.9) was studied by circular dichroism (CD) spectroscopy in the ultraviolet. The conformation of the polynucleotide, as reflected by its chiroptical signature, changes in a highly cooperative fashion in the presence of Hg(ClO4)2. The CD changes signal transitions first from the B to a modified B-state (B*), or to a non-B structure termed X, and finally to a form that is presumably Z. The alterations are totally reversible subsequent to the removal of mercury with the help of a suitable complexing agent such as sodium cyanide, indicating that mercuration does not disrupt Watson-Crick hydrogen bonding to any extent.
通过紫外圆二色光谱(CD)研究了聚[d(T-G)·d(C-A)]在水溶液(0.1 M高氯酸钠,5 mM二甲胂酸缓冲液,pH 6.9)中的构象。在Hg(ClO4)2存在下,多核苷酸的构象(由其手性光学特征反映)以高度协同的方式发生变化。CD变化信号首先从B态转变为修饰的B态(B*),或转变为一种称为X的非B结构,最终转变为可能是Z的形式。在使用合适的络合剂(如氰化钠)除去汞之后,这些变化是完全可逆的,这表明汞化在任何程度上都不会破坏沃森-克里克氢键。