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静压对 DNA 发夹热稳定性的影响。

The effect of hydrostatic pressure on the thermal stability of DNA hairpins.

机构信息

Graduate Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Canada.

出版信息

Biophys Chem. 2011 Jun;156(1):88-95. doi: 10.1016/j.bpc.2011.02.001. Epub 2011 Feb 15.

Abstract

DNA hairpins consist of two distinct structural domains: a double stranded stem and a single-stranded loop that connect the two strands of the stem. Previous studies of short DNA hairpins have revealed that loop and stem sequences can significantly affect the thermodynamic stability of short DNA hairpins. In this work we present the effect of hydrostatic pressure on the helix-coil transition temperature (T(M)) for 11 16-base, hairpin-forming DNA oligonucleotides. All of the samples form a hairpin with a 6-base pair stem and a four-base loop. In addition, the four base pairs at the end of the stem distal from the loop are the same for every molecule. We have varied loop sequence and identity of the two duplex base pairs adjacent to the loop. Using the change in UV absorption to monitor the conformational state of the oligonucleotide the hairpin-coil transition temperature of these molecules was studied as a function of sodium ion concentration and pressure. From these data we calculated the volume change accompanying the transition. Model-dependent (van't Hoff) transition parameters such as ΔH(vH) and transition volume (ΔV) were estimated from the analysis of conformational transitions. Experiments revealed that the ΔV for denaturation of these molecules range from -2.35 to +6.74 cm(3) mol(-1). The expansibility (ΔΔV/ΔT) and the pressure dependence of cation release are also presented. The difference in the volume change for this transition is related to the differences in the hydration of these molecules.

摘要

DNA 发夹由两个不同的结构域组成:双链茎和单链环,连接茎的两条链。先前对短 DNA 发夹的研究表明,环和茎序列可以显著影响短 DNA 发夹的热力学稳定性。在这项工作中,我们研究了静水压力对 11 个 16 碱基、发夹形成 DNA 寡核苷酸的螺旋-卷曲转变温度 (T (M)) 的影响。所有样品都形成一个茎为 6 个碱基对、环为 4 个碱基对的发夹。此外,远离环的茎末端的四个碱基对对于每个分子都是相同的。我们改变了环序列和环附近的两个双螺旋碱基对的身份。通过监测寡核苷酸构象状态的紫外吸收变化,研究了这些分子的发夹-卷曲转变温度作为钠离子浓度和压力的函数。从这些数据中,我们计算了伴随转变的体积变化。从构象转变的分析中,估计了模型相关(范特霍夫)转变参数,如 ΔH (vH) 和转变体积 (ΔV)。实验表明,这些分子的变性 ΔV 范围为-2.35 至+6.74 cm 3 mol -1。还介绍了可扩展性(ΔΔV/ΔT)和阳离子释放的压力依赖性。这个转变的体积变化差异与这些分子的水合差异有关。

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