Fazakerley G V, Russell J C, Wolfe M A
Eur J Biochem. 1977 Jun 15;76(2):601-5. doi: 10.1111/j.1432-1033.1977.tb11630.x.
The aqueous solution conformation of four purine 3':5'-nucleotides varying in their substituents at C-6 and C-8 has been studied using gadolinium(III) to perturb the proton relaxation times. The ribose conformations are inferred. All the nucleotides are best described as being in a dynamic equilibrium between syn and anti conformations and the position of this equilibrium is not dramatically affected by changing the substituent at C-6. These nucleotides in their neutral base form slightly favour an anti conformation. In the presence of a bulky methylthio group at C-8 the equilibrium is shifted towards a dominance from the syn conformation due to steric repulsion factors.
利用钆(III)干扰质子弛豫时间,研究了四种在C-6和C-8处取代基不同的嘌呤3':5'-核苷酸的水溶液构象。推断出了核糖构象。所有核苷酸最好被描述为处于顺式和反式构象之间的动态平衡中,并且这种平衡的位置不会因改变C-6处的取代基而受到显著影响。这些中性碱基形式的核苷酸略微倾向于反式构象。在C-8处存在庞大的甲硫基时,由于空间排斥因素,平衡向顺式构象占主导的方向移动。