Allen F S, Jones M B, Hollstein U
Biophys J. 1977 Oct;20(1):69-78. doi: 10.1016/S0006-3495(77)85537-9.
The circular dichroism spectra of eleven double-stranded DNAs, five natural with known nearest neighbor frequencies and six synthetic polydimers and polytrimers, were measured from 210 to 310 nm in the absence and presence of increasing amounts of actinomycin up to saturation. Based on the fact that the circular dichroism of nucleic acids is a nearest-neighbor frequency-dependent property, matrix analysis of the problem revealed which neighbor sets were perturbed by actinomycin, presumably by intercalation of the planar moiety of the molecule. The intercalation sites can be separated into three families. The first-neighbor units GpC and CpG are very favorable binding sites for actinomycin. ApG, CpC, ApC, TpC, and TpG appear to be less attractive sites, while ApT, TpA, and ApA are unfavorable sites.
在不存在放线菌素以及存在逐渐增加直至饱和量的放线菌素的情况下,测量了11种双链DNA的圆二色光谱,其中5种是具有已知最近邻频率的天然双链DNA,6种是合成的多聚二核苷酸和多聚三核苷酸,测量范围为210至310纳米。基于核酸的圆二色性是一种依赖于最近邻频率的特性这一事实,对该问题的矩阵分析揭示了哪些相邻碱基对被放线菌素干扰,推测是由于该分子平面部分的嵌入作用。嵌入位点可分为三类。第一邻位单元GpC和CpG是放线菌素非常有利的结合位点。ApG、CpC、ApC、TpC和TpG似乎是吸引力较小的位点,而ApT、TpA和ApA是不利位点。