Chinsky L, Turpin P Y
Nucleic Acids Res. 1978 Aug;5(8):2969-77. doi: 10.1093/nar/5.8.2969.
The DNA-Actinomycin D interaction has been studied by resonance Raman effect using DNA as chromophore. First, the resonance Raman spectra of DNA obtained with a U.V. excitation at wavelengths of 300 nm and 280 nm are presented. The main Raman hands are assigned to the convenient nucleic bases by comparison with the spectra of mononucleotides obtained under the same experimental conditions. In particular, with a 300 nm excitation, the 1582 cm-1 line is provided by adenine, while the 1492 cm-1 one is almost exclusively due to guanine. Then, the DNA-Actinomycin D complex has been studied: the line enhancements and the specificity of the resonance permits the displaying of the DNA spectrum free of any contribution of Actinomycin. The interaction provides a large intensity decrease of the 1492 cm-1 guanine line: this is a direct consequence of the orbital overlapping of the guanine 2-aminogroup with the ring nitrogen of Actinomycin in the DNA-Actinomycin pi complex.
利用DNA作为发色团,通过共振拉曼效应研究了DNA与放线菌素D的相互作用。首先,给出了在300nm和280nm波长的紫外激发下获得的DNA共振拉曼光谱。通过与在相同实验条件下获得的单核苷酸光谱进行比较,将主要的拉曼谱带归属于相应的核酸碱基。特别是,在300nm激发下,1582cm-1谱线由腺嘌呤产生,而1492cm-1谱线几乎完全归因于鸟嘌呤。然后,对DNA-放线菌素D复合物进行了研究:谱线增强和共振特异性使得能够展示出不含放线菌素任何贡献的DNA光谱。这种相互作用导致1492cm-1鸟嘌呤谱线强度大幅降低:这是DNA-放线菌素π复合物中鸟嘌呤2-氨基基团与放线菌素环氮的轨道重叠的直接结果。