Charney E, Chen H H, Rau D C
Laboratory of Chemical Physics, NIDDK, National Institutes of Health, Besthesda, Maryland 20892.
J Biomol Struct Dyn. 1991 Oct;9(2):353-62. doi: 10.1080/07391102.1991.10507917.
We have determined the rise per base pair and persistence length of A-form DNA in trifluoroethanol solutions for fragments 350-900 base pairs in length that best describe rotational diffusion coefficients determined by transient electric birefringence. The 2.6 A spacing between base pairs found in crystal and fiber A-form structures is preserved in solution. The persistence length is about 1500 A, or about three times longer than for B-form DNA. There is no apparent electrostatic contribution to the persistence length in the salt concentration range 0.2-2.0 mM Na cacodylate. This suggests an even closer association between DNA and its neutralizing counterions than predicted by condensation theory, perhaps due to a sheath of trifluoroethanol excluded water surrounding the A-form helix.
我们已经确定了三氟乙醇溶液中长度为350 - 900个碱基对的A-DNA每碱基对的上升高度和持久长度,这能最好地描述由瞬态电双折射测定的旋转扩散系数。在晶体和纤维A-DNA结构中发现的碱基对之间2.6 Å的间距在溶液中得以保留。持久长度约为1500 Å,约为B-DNA的三倍。在0.2 - 2.0 mM二甲胂酸钠盐浓度范围内,持久长度没有明显的静电贡献。这表明DNA与其中和抗衡离子之间的结合比凝聚理论预测的更为紧密,这可能是由于围绕A-DNA螺旋的三氟乙醇排斥水鞘所致。