Hsieh T S, Wang J C
Biochemistry. 1975 Feb 11;14(3):527-35. doi: 10.1021/bi00674a011.
Binding isotherms of ethidium to the superhelical DNA from phage PM2, and to PM2 DNA containing -1 single-chain scission per molecule, have been determined at six temperatures from 2.5 to 50 degrees, in 3M CsCl-0.01 M Na3EDTA. Spectrophotometric measurements in both the visible and ultraviolet (uv) regions were used to obtain the binding isotherms. The isotherm at 20 degrees was also obtained by determining the free ethidium concentrations in equilibrium with DNA-ethidium complexes in boundary sedimentation experiments. A simple thermodynamic analysis shows that for a superhelical DNA with v bound ethidium per nucleotide, the change in free energy per unit change in the number of superhelical turns T, dGT/dT, is directly related the ratio of the free ethidium concentrations, cf,v and cf,v, in equilibrium with the ethidium complexes of the superhelical and the nicked DNA, respectively, at the same values of v. The relationship is dGT/dT = (360/E)RTln (cf,v/cf,v), where e is the unwinding angle of the DNA helix per bound ethidium molecule. Experimentally, it was found that ln (cf,v/cf,v) = a1(v - vc), where a1 is a constant at a given temperature and vc is the value of v at which the originally superhelical DNA is completely relaxed, i.e., containing no superhelical turns. The equation relating dGT/dT and v, upon transformation and integration, gives finite difference GT,v=o = -a1NRTvc2/2, where finite difference GT,v=0 is the free energy of superhelix formation of the superhelical DNA in the absence of ethidium and N is the number of nucleotides per DNA molecule. This equation is independent of the unwinding angle e. The values of a1 are 11.2 plus or minus 0.9, 11.2 plus or minus 0.7, 11.2 plus or minus 0.6, 10.7 plus or minus 0.8, 10.0 pl.us or minus 1.0, and 9.8 plus or minus 1.4 at 2.5, 10, 20, 30, 40, and 50 degrees, respectively. Measurements with lambda b2b5c DNA, and monomeric and trimeric lambda dv DNA, indicate that the constant a1 is insensitive to the molecular length of DNA. The present results are compared with the previous results of Bauer and Vinograd (Bauer, W., and Vinograd, M. (1970), J. Mol. Biol. 47, 419), obtained by a statistical mechanical analysis of the ethidium binding isotherms (determined by density gradient centrifugation measurements) to two forms of simian virus 40 DNA at 25 degrees. The effects of superhelical turns on a number of processes, such as the binding of a ligand which unwinds or winds the DNA helix, the denaturation of a DNA segment, and the formation of hair-pinned structures from base sequences with a twofold rotational symmetry, are discussed from the thermodynamic point of view, based on the present results.
已在3M CsCl - 0.01M Na3EDTA中,于2.5至50摄氏度的六个温度下测定了溴化乙锭与噬菌体PM2的超螺旋DNA以及与每个分子含有-1个单链断裂的PM2 DNA的结合等温线。利用可见和紫外(uv)区域的分光光度测量来获得结合等温线。20摄氏度时的等温线还通过在边界沉降实验中测定与DNA - 溴化乙锭复合物处于平衡状态的游离溴化乙锭浓度而得到。一个简单的热力学分析表明,对于每个核苷酸结合v个溴化乙锭的超螺旋DNA,超螺旋圈数T每单位变化时自由能的变化dGT/dT,与分别在相同v值下与超螺旋DNA和带切口DNA的溴化乙锭复合物处于平衡状态的游离溴化乙锭浓度cf,v和cf,v的比值直接相关。该关系为dGT/dT = (360/E)RTln (cf,v/cf,v),其中e是每个结合的溴化乙锭分子使DNA螺旋解旋的角度。实验发现,ln (cf,v/cf,v) = a1(v - vc),其中a1是给定温度下的常数,vc是最初的超螺旋DNA完全松弛时v的值,即不包含超螺旋圈。将dGT/dT与v相关的方程进行变换和积分后,得到有限差分GT,v=o = -a1NRTvc2/2,其中有限差分GT,v=0是在不存在溴化乙锭时超螺旋DNA形成超螺旋的自由能,N是每个DNA分子的核苷酸数。该方程与解旋角e无关。a1在2.5、10、20、30、40和50摄氏度时的值分别为11.2 ± 0.9、11.2 ± 0.7、11.2 ± 0.6、10.7 ± 0.8、10.0 ± 1.0和9.8 ± 1.4。用λ b2b5c DNA以及单体和三聚体λ dv DNA进行的测量表明,常数a1对DNA的分子长度不敏感。将目前的结果与Bauer和Vinograd先前的结果(Bauer, W., and Vinograd, M. (1970), J. Mol. Biol. 47, 419)进行了比较,他们通过对25摄氏度下两种形式的猴病毒40 DNA的溴化乙锭结合等温线(由密度梯度离心测量确定)进行统计力学分析而得到该结果。基于目前的结果,从热力学角度讨论了超螺旋圈对许多过程的影响,如解开或缠绕DNA螺旋的配体的结合、DNA片段的变性以及由具有双重旋转对称性的碱基序列形成发夹结构等。