Yamaoka Kiwamu
Colloids Surf B Biointerfaces. 2007 Apr 15;56(1-2):97-106. doi: 10.1016/j.colsurfb.2006.12.008. Epub 2006 Dec 20.
Anomalous electric birefringence signals of a sonicated and column-fractionated medium-size calf thymus DNA sample (bp=570) in Na(+) solutions were measured at 7 degrees C. The reversing-pulse electric birefringence (RPEB) signal pattern was theoretically calculated in the low electric field region for two axially symmetric models coexisting in equilibrium in solution. The RPEB theory is based on the electric dipole moment due to ion-fluctuation along the longitudinal direction and the electric polarizability anisotropy (Deltaalpha'), together with various electric and optical parameters assigned to the models. An analytical method was developed for the steady-state birefringence of the two-component system in a wide range of electric fields. The NaDNA samples exhibit complex RPEB patterns mixed with negative- and positive-going profiles. An experimental RPEB signal of NaDNA at an absorbance (A(260)) of 8 was fitted to theoretical curve at weak electric fields. The anomalous RPEB signal was attributed to the component 2, which shows a dip in the buildup and another in the reverse processes with a positive sign and a larger relaxation time. For the component 1, a normal DNA profile with negative sign is associated with a narrow dip in the reverse and a faster relaxation time in the decay signal. The field-strength dependence of observed steady-state birefringence delta(infinity) could be fitted for NaDNA at A(260)=8 by the SUSID orientation function with saturated ionic and electronic moments. An apparent positive maximum and the sign reversal in delta(infinity) at weak electric fields is an interplay between the positive component 2 with positive optical factor Deltag and negative Deltaalpha' and the negative component 1 with negative Deltag and positive Deltaalpha'. Possible conformation of two DNA components involved in solution was estimated.
在7摄氏度下测量了超声处理并经柱分级分离的中等大小小牛胸腺DNA样品(碱基对=570)在Na(+)溶液中的异常电双折射信号。针对溶液中平衡共存的两个轴对称模型,在低电场区域理论计算了反向脉冲电双折射(RPEB)信号模式。RPEB理论基于沿纵向的离子涨落引起的电偶极矩和电极化率各向异性(Δα'),以及赋予模型的各种电学和光学参数。开发了一种分析方法来处理宽电场范围内双组分系统的稳态双折射。NaDNA样品呈现出混合了正向和负向轮廓的复杂RPEB模式。在弱电场下,将吸光度(A(260))为8时NaDNA的实验RPEB信号拟合到理论曲线上。异常的RPEB信号归因于组分2,它在积累过程中有一个凹陷,在反向过程中有另一个凹陷,符号为正,弛豫时间更长。对于组分1,具有负号的正常DNA轮廓与反向过程中的窄凹陷以及衰减信号中更快的弛豫时间相关。通过具有饱和离子和电子矩的SUSID取向函数,可以拟合A(260)=8时NaDNA的观测稳态双折射δ(∞)的场强依赖性。在弱电场下,δ(∞)中明显的正最大值和符号反转是具有正光学因子Δg和负Δα'的正组分2与具有负Δg和正Δα'的负组分1之间相互作用的结果。估计了溶液中涉及的两种DNA组分的可能构象。