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用单分子力谱技术探测 DNA 夹。

Probing DNA clamps with single-molecule force spectroscopy.

机构信息

Department of Chemistry, the Pennsylvania State University, University Park, PA 16802, USA and Department of Chemistry, Georgia State University, Atlanta, GA 30302, USA.

出版信息

Nucleic Acids Res. 2013 Sep;41(16):7804-14. doi: 10.1093/nar/gkt487. Epub 2013 Jun 19.

Abstract

Detailed mechanisms of DNA clamps in prokaryotic and eukaryotic systems were investigated by probing their mechanics with single-molecule force spectroscopy. Specifically, the mechanical forces required for the Escherichia coli and Saccharomyces cerevisiae clamp opening were measured at the single-molecule level by optical tweezers. Steered molecular dynamics simulations further examined the forces involved in DNA clamp opening from the perspective of the interface binding energies associated with the clamp opening processes. In combination with additional molecular dynamics simulations, we identified the contact networks between the clamp subunits that contribute significantly to the interface stability of the S.cerevisiae and E. coli clamps. These studies provide a vivid picture of the mechanics and energy landscape of clamp opening and reveal how the prokaryotic and eukaryotic clamps function through different mechanisms.

摘要

通过单分子力谱技术研究了原核和真核系统中 DNA 夹的详细机制。具体来说,通过光学镊子在单分子水平上测量了大肠杆菌和酿酒酵母夹的打开所需的机械力。定向分子动力学模拟进一步从与夹打开过程相关的界面结合能的角度研究了 DNA 夹打开涉及的力。结合其他分子动力学模拟,我们确定了在酿酒酵母和大肠杆菌夹的界面稳定性中起重要作用的夹亚基之间的接触网络。这些研究提供了夹打开的力学和能量景观的生动画面,并揭示了原核和真核夹如何通过不同的机制发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46fb/3763527/ab7b52b0fffb/gkt487f1p.jpg

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