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通过电子显微镜分析二聚体DNA连环体的结构。

Analysis of the structure of dimeric DNA catenanes by electron microscopy.

作者信息

Levene S D, Donahue C, Boles T C, Cozzarelli N R

机构信息

Program in Molecular and Cell Biology, University of Texas at Dallas, Richardson 75083, USA.

出版信息

Biophys J. 1995 Sep;69(3):1036-45. doi: 10.1016/S0006-3495(95)79978-7.

Abstract

We analyzed the structure of open-circular and supercoiled dimeric DNA catenanes generated by site-specific recombination in vitro. Electron microscopy of open-circular catenanes shows that the number of duplex crossings in a plane is a linear function of the number of catenane interlinks (Ca/2), and that the length of the catenane axis is constant, independent of Ca. These relationships are similar to those observed with supercoiled DNA. Statistical analyses reveal, however, that the conformations of the individual rings of the catenanes are similar to those of unlinked circles. The distribution of distances between randomly chosen points on separate rings depends strongly on Ca and is consistent with a sharp decrease in the center-of-mass separation between rings with increasing Ca. Singly linked supercoiled catenanes are seen by microscopy to be linked predominantly through terminal loops in the respective superhelices. The observations suggest that chain entropy is a major factor determining the conformation of DNA catenanes.

摘要

我们分析了体外位点特异性重组产生的开环和超螺旋二聚体DNA连环体的结构。对开环连环体的电子显微镜观察表明,平面内双链交叉的数量是连环体交联数(Ca/2)的线性函数,并且连环体轴的长度是恒定的,与Ca无关。这些关系与超螺旋DNA观察到的关系相似。然而,统计分析表明,连环体单个环的构象与未连接环的构象相似。不同环上随机选择点之间的距离分布强烈依赖于Ca,并且与随着Ca增加环之间质心间距急剧减小一致。通过显微镜观察,单链连接的超螺旋连环体主要通过各自超螺旋中的末端环连接。这些观察结果表明链熵是决定DNA连环体构象的主要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3bc/1236332/dfda803d0eb6/biophysj00057-0302-a.jpg

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