Nordenskiöld L, Chang D K, Anderson C F, Record M T
Biochemistry. 1984 Sep 11;23(19):4309-17. doi: 10.1021/bi00314a009.
NMR relaxation rates (T1(-1) and T2(-1)) have been determined for 23Na in aqueous salt solutions containing various types of helical double-stranded deoxyribonucleic acids. These measurements were performed on three synthetic polynucleotides having different overall conformations, poly-(dA-dT).poly(dA-dT) (alternating B-DNA), poly(dG-dC).poly(dG-dC) at low salt (B-DNA), and Br-poly(dG-dC).Br-poly(dG-dC) (left-handed Z-DNA), and on four types of natural DNA differing in base composition, Clostridium perfringens (26% GC), calf thymus (40% GC), Escherichia coli (50% GC), and Micrococcus lysodeikticus (72% GC). For all types of DNA investigated, except poly(dA-dT).poly(dA-dT), the 23Na NMR spectra measured at 21 degrees C and an applied field of 4.7 T are non-Lorentzian. These non-Lorentzian spectra were analyzed on the basis of the two-state model and the standard theory of nonexponential quadrupolar relaxation processes in order to obtain estimates of the correlation times (tau c) characteristic of the sodium nuclei associated with the various nucleic acids. All of the correlation times estimated in this way are in the range of nanoseconds. The magnitudes of these correlation times show a significant dependence on the overall conformation of the nucleic acid (B vs. Z) but not on its base composition. To investigate the concentration dependence of tau c, sodium or magnesium salts were added to solutions of Br-poly(dG-dC).Br-poly(dG-dC) (Z-DNA).(ABSTRACT TRUNCATED AT 250 WORDS)
已测定了含各种类型螺旋双链脱氧核糖核酸的盐水溶液中23Na的核磁共振弛豫率(T1(-1)和T2(-1))。这些测量是在三种具有不同整体构象的合成多核苷酸上进行的,即聚(dA-dT)·聚(dA-dT)(交替B-DNA)、低盐浓度下的聚(dG-dC)·聚(dG-dC)(B-DNA)和溴化聚(dG-dC)·溴化聚(dG-dC)(左手Z-DNA),以及在四种碱基组成不同的天然DNA上进行的,即产气荚膜梭菌(26%GC)、小牛胸腺(40%GC)、大肠杆菌(50%GC)和解淀粉芽孢杆菌(72%GC)。对于所研究的所有类型的DNA,除了聚(dA-dT)·聚(dA-dT),在21摄氏度和4.7T的外加磁场下测得的23Na核磁共振谱是非洛伦兹的。基于双态模型和非指数四极弛豫过程的标准理论对这些非洛伦兹谱进行了分析,以便获得与各种核酸相关的钠核特征相关时间(τc)的估计值。以这种方式估计的所有相关时间都在纳秒范围内。这些相关时间的大小显示出对核酸的整体构象(B型与Z型)有显著依赖性,但对其碱基组成没有依赖性。为了研究τc的浓度依赖性,将钠盐或镁盐添加到溴化聚(dG-dC)·溴化聚(dG-dC)(Z-DNA)溶液中。(摘要截断于250字)