Wu P G, Song L, Clendenning J B, Fujimoto B S, Benight A S, Schurr J M
Department of Chemistry, University of Washington, Seattle 98195.
Biochemistry. 1988 Oct 18;27(21):8128-44. doi: 10.1021/bi00421a023.
The magnitude and uniformity of the torsion elastic constant (alpha) of linear pBR322 DNA and supercoiled pBR322 DNAs with high-twist (sigma = -0.083) and normal-twist (sigma = -0.48) are measured in 0.1 M NaCl as a function of added chloroquine/base-pair ratio (chl/bp) by studying the fluorescence polarization anisotrophy (FPA) of intercalated ethidium dye. The time-resolved FPA is measured by using a picosecond dye laser for excitation and time-correlated single-photon counting detection. A general theory is developed for the binding of ligands that unwind superhelical DNAs, and the simultaneous binding of two different intercalators is treated in detail. The equilibrium constant (K) for binding chloroquine to linear pBR322 DNA and the number (r) of bound chloroquines per base pair are determined from the relative amplitude ratio of the slow (normally intercalated) and fast (free) components in the decay of the (probe) ethidium fluorescence intensity as a function of chl/bp. For chloroquine binding to supercoiled pBR322 DNAs, the intrinsic binding constant is assumed to be the same as for the linear DNA, but the twist energy parameter ET (N times the free energy to change the linking number from 0 to 1 in units of kBT) is regarded as adjustable. Using the best-fit ET, the binding ratios r are calculated for each chl/bp ratio. Twist energy parameters are also determined for ethidium binding to these supercoiled DNAs by competitive dialysis. For chloroquine binding, we obtain ET = 360 and 460 respectively for the normal-twist and high-twist supercoiled DNAs. For ethidium binding the corresponding values are ET = 280 +/- 70 and 347 +/- 50. Like other dye-binding values, these are substantially lower than those obtained by ligation methods. In the absence of chloroquine, the torsion constants of all three DNAs are virtually identical, alpha = (5.0 +/- 0.4) x 10(-12) dyn.cm. For linear pBR322 DNA, the magnitude and uniformity of alpha remain unaltered by intercalated chloroquine up to r = 0.19. This finding argues that the FPA is not significantly relaxed by diffusion of any kinks or solitons. If alpha d denotes the torsion constant between a dye and a base pair and alpha 0 that between two base pairs, then our data imply that alpha d/alpha 0 lies in the range 0.65-1.64, with a most probable value of 1.0.(ABSTRACT TRUNCATED AT 400 WORDS)
通过研究嵌入的溴化乙锭染料的荧光偏振各向异性(FPA),在0.1 M NaCl中测量线性pBR322 DNA以及具有高扭曲(σ = -0.083)和正常扭曲(σ = -0.48)的超螺旋pBR322 DNA的扭转弹性常数(α)的大小和均匀性,该测量是作为添加的氯喹/碱基对比率(chl/bp)的函数进行的。使用皮秒染料激光器进行激发并采用时间相关单光子计数检测来测量时间分辨FPA。针对使超螺旋DNA解旋的配体结合,建立了一个通用理论,并详细处理了两种不同嵌入剂的同时结合。氯喹与线性pBR322 DNA结合的平衡常数(K)以及每碱基对结合氯喹的数量(r),是根据(探针)溴化乙锭荧光强度衰减中慢(通常为嵌入)和快(游离)成分的相对振幅比作为chl/bp的函数来确定的。对于氯喹与超螺旋pBR322 DNA的结合,假定其固有结合常数与线性DNA相同,但扭转能量参数ET(以kBT为单位将连接数从0改变为1的自由能的N倍)被视为可调整的。使用最佳拟合的ET,计算每个chl/bp比率下的结合比率r。还通过竞争性透析确定了溴化乙锭与这些超螺旋DNA结合的扭转能量参数。对于氯喹结合,我们分别得到正常扭曲和高扭曲超螺旋DNA的ET = 360和460。对于溴化乙锭结合,相应的值为ET = 280±70和347±50。与其他染料结合值一样,这些值明显低于通过连接方法获得的值。在不存在氯喹的情况下,所有三种DNA的扭转常数实际上是相同的,α =(5.0±0.4)×10^(-12) dyn.cm。对于线性pBR322 DNA,直到r = 0.19,嵌入氯喹后α的大小和均匀性保持不变。这一发现表明,任何扭结或孤子的扩散都不会使FPA显著松弛。如果αd表示染料与碱基对之间的扭转常数,α0表示两个碱基对之间的扭转常数,那么我们的数据意味着αd/α0在0.65 - 1.64范围内,最可能的值为1.0。(摘要截断于400字)