Kubasek W L, Hudson B, Peticolas W L
Proc Natl Acad Sci U S A. 1985 Apr;82(8):2369-73. doi: 10.1073/pnas.82.8.2369.
Raman spectra are presented for dilute aqueous solutions of the four ribonucleotides AMP, GMP, UMP, and CMP obtained with laser excitation at 299, 266, 253, 240, 229, 218, 209, and 200 nm. Distinct evidence of strong, selective resonance enhancement is obtained. Low-resolution excitation profiles have been constructed for the strongest bands by using the phosphate band at 994 cm-1 as an internal reference. The excitation spectra for many of the vibrational bands are dominated by a peak corresponding to the lowest-energy electronic transition near 260 nm. Smaller peaks are seen for higher-energy electronic transitions. For some modes, the resonance enhancement is dominated by the higher-energy transitions. It is clear from these new data that a full description of the resonance Raman profiles of the nucleic acids will have to include several excited electronic states. Two examples are given of cases where ionic species can be distinguished easily by using far-UV excitation, but these species are indistinguishable with 266-nm excitation. This demonstrates the utility of far-UV resonance Raman spectroscopy for obtaining structural information.
给出了用299、266、253、240、229、218、209和200nm激光激发获得的四种核糖核苷酸AMP、GMP、UMP和CMP的稀水溶液的拉曼光谱。获得了强选择性共振增强的明显证据。通过使用994cm-1处的磷酸盐带作为内参,构建了最强谱带的低分辨率激发谱。许多振动谱带的激发光谱由一个对应于260nm附近最低能量电子跃迁的峰主导。对于更高能量的电子跃迁,可以看到较小的峰。对于某些模式,共振增强由更高能量的跃迁主导。从这些新数据可以清楚地看出,对核酸共振拉曼谱的完整描述必须包括几个激发电子态。给出了两个例子,在这两种情况下,通过使用远紫外激发可以很容易地区分离子物种,但在266nm激发下这些物种无法区分。这证明了远紫外共振拉曼光谱在获取结构信息方面的实用性。