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Low angle light scattering studies on whole half and quarter molecules of T2 bacteriophage DNA.

机译:对T2噬菌体DNA的全部一半和四分之一分子进行低角度光散射研究。

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摘要

Static light scattering measurements have been made at angles as low as 8 degrees on whole, half, and quarter molecules of native, T2 bacteriophage DNA in 0.195 M Na+. The fragments were obtained by high-speed stirring of the native DNA, and fractionated on methylated-albumin-kieselguhr columns. Accompanying measurements of sedimentation coefficients and intrinsic viscosities were made. Because linear extrapolations of light scattering data above 8 degrees for these samples were suspect, the measurements were analyzed by fitting curves calculated from the theory of wormlike coils to experimental curves at c = 0. Results showed that the excluded volume parameter, epsilon, must be used in analyzing the scattering curves; a reasonable value of epsilon was 0.08, in agreement with that found for T7 DNA (Harpst, J. A. 1980. Biophys. Chem. 11:295-302). The persistence length of all three DNAs in this paper was 50 +/- 5 nm, showed no dependence on molecular weight, but was somewhat below that reported previously for T7 DNA (60 nm). Theoretical curves calculated with the preceding parameters had a clear upward curvature in scattering envelopes below 8 degrees for quarter and half molecules, but such curvature was minimal for whole T2 DNA, so that linear extrapolations of experimental data above 8 degrees gave a molecular weight and root-mean-square radius which were nearly the same as those from theory. The molecular weight and radius for whole T2, derived from the comparison of theory and experiment, were 115 X 10(6) and 1,224 nm, respectively. The measurements on T2 DNA were clearly at the upper limit of current techniques.
机译:在0.195 M Na +中,天然T2噬菌体DNA的全部,一半和四分之一分子的静态光散射测量值低至8度。通过天然DNA的高速搅拌获得片段,并在甲基化的白蛋白-kieselguhr柱上分级分离。进行了沉积系数和固有粘度的测量。由于怀疑这些样品在8度以上的光散射数据是线性外推的,因此通过根据蠕虫状线圈理论计算出的曲线与c = 0时的实验曲线拟合来分析测量结果。结果表明必须排除体积参数epsilon用于分析散射曲线; ε的合理值是0.08,与T7 DNA的值一致(Harpst,J.A.1980.Biophys.Chem.11:295-302)。本文中所有三个DNA的持久长度为50 +/- 5 nm,不依赖于分子量,但略低于先前报道的T7 DNA(60 nm)。对于四分之一和一半的分子,使用上述参数计算的理论曲线在低于8度的散射包膜中具有明显的向上曲率,但是对于整个T2 DNA而言,这种曲率最小,因此,对8度以上的实验数据进行线性外推可得出分子量和根-均方根半径与理论值几乎相同。从理论和实验的比较得出,整个T2的分子量和半径分别为115 X 10(6)和1,224 nm。 T2 DNA的测量显然处于当前技术的上限。

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