Piana Stefano
Department of Applied Chemistry, Nanochemistry Research Institute, Curtin University of Technology, GPO Box U1987, Perth 6845, Western Australia.
Nucleic Acids Res. 2005 Dec 14;33(22):7029-38. doi: 10.1093/nar/gki1010. Print 2005.
In the last decade, methods to study single DNA molecules under tensile load have been developed. These experiments measure the force required to stretch and melt the double helix and provide insights into the structural stability of DNA. However, it is not easy to directly relate the shape of the force curve to the structural changes that occur in the double helix under tensile load. Here, state-of-the-art computer simulations of short DNA sequences are preformed to provide an atomistic description of the stretching of the DNA double helix. These calculations show that for extensions larger that approximately 25% the DNA undergoes a structural transformation and a few base pairs are lost from both the terminal and central part of the helix. This locally melted DNA duplex is stable and can be extended up to approximately 50-60% of the equilibrium length at a constant force. It is concluded that melting under tension cannot be modeled as a simple two-state process. Finally, the important role of the cantilever stiffness in determining the shape of the force-extension curve and the most probable rupture force is discussed.
在过去十年中,已经开发出了在拉伸载荷下研究单个DNA分子的方法。这些实验测量拉伸和熔解双螺旋所需的力,并提供有关DNA结构稳定性的见解。然而,将力曲线的形状与拉伸载荷下双螺旋中发生的结构变化直接联系起来并非易事。在此,对短DNA序列进行了最先进的计算机模拟,以提供DNA双螺旋拉伸的原子描述。这些计算表明,当延伸率大于约25%时,DNA会发生结构转变,并且从螺旋的末端和中心部分都会丢失一些碱基对。这种局部熔解的DNA双链体是稳定的,并且在恒定力作用下可以延伸至平衡长度的约50 - 60%。得出的结论是,张力下的熔解不能被建模为简单的双态过程。最后,讨论了悬臂刚度在确定力 - 延伸曲线形状和最可能的断裂力方面的重要作用。