Miles H T, Frazier J
Biochemistry. 1978 Jul 11;17(14):2920-7. doi: 10.1021/bi00607a034.
Strong absorbance of water at 1645 cm-1 has previously prevented dependable observation of infrared spectra of H2O solutions in the carbonyl region. We have obtained reliable spectra in pure water and in alcohol-water mixtures in this region and used them to study A.U polynucleotide interaction. Spectra in pure water were obtained by computer subtraction of solvent from that of solution measured in short path length cells. Mixed solvents, by diluting the water, permit use of longer cells and standard double-beam compensation methods. Poly(adenylic acid) in H20 solution has a strong NH2 deformation band at 1659 cm-1 coupled to an A ring vibration at 1605 cm-1. Poly(uridylic acid) has a broad band at approximately 1695 cm-1, predominantly C2 carbonyl stretch, an unresolved CR carbonyl band (probably near 1660 cm-1), and a ring vibration at approximately 1636 cm-1. The large changes these spectra undergo when helical structures are formed are discussed and compared with changes observed in D2O.
此前,水在1645厘米-1处的强吸收阻碍了对羰基区域H2O溶液红外光谱的可靠观测。我们已在该区域获得了纯水和醇-水混合物的可靠光谱,并利用它们来研究A.U多核苷酸相互作用。纯水中的光谱是通过计算机从在短光程池中测量的溶液光谱中减去溶剂光谱得到的。混合溶剂通过稀释水,使得可以使用更长的光程池和标准双光束补偿方法。H2O溶液中的聚腺苷酸在1659厘米-1处有一个强的NH2变形带,与1605厘米-1处的A环振动相关联。聚尿苷酸在约1695厘米-1处有一个宽带,主要是C2羰基伸缩振动,一个未分辨的CR羰基带(可能在1660厘米-1附近),以及在约1636厘米-1处的环振动。讨论了这些光谱在形成螺旋结构时所经历的巨大变化,并与在D2O中观察到的变化进行了比较。