Microscopic analysis of DNA and DNA-protein assembly by transmission electron microscopy, scanning tunneling microscopy and scanning force microscopy

被引:0
|
作者
Müller-Reichert, T [1 ]
Gross, H [1 ]
机构
[1] European Mol Biol Lab, D-69112 Heidelberg, Germany
来源
SCANNING MICROSCOPY SUPPLEMENT 10, 1996: THE SCIENCE OF BIOLOGICAL SPECIMEN PREPARATION FOR MICROSCOPY | 1996年
关键词
transmission electron microscopy; scanning electron microscopy; scanning tunneling microscopy; scanning force microscopy; DNA; DNA-protein interaction; Repressor Activator Protein (RAP) 1;
D O I
暂无
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To investigate DNA and DNA-protein assembly, nucleic acids were adsorbed to freshly cleaved mica in the presence of magnesium ions. The efficiency of DNA adhesion and the distribution of the molecules on the mica surface were checked by transmission electron microscopy. In addition, various kinds of DNA-protein interactions including DNA wrapping and DNA supercoiling were analyzed using electron microscopy. In parallel, this Mg2+/mica method can be applied (1) to analyze embedded DNA by scanning tunneling microscopy, (2) to visualize freeze-dried, metal coated DNA-protein complexes by tunneling microscopy, and (3) to image DNA or DNA-protein interaction in air or in liquid by scanning force microscopy. An advantage of such a correlative approach is that parallel imaging can reveal complementary information. The benefit of such a combined approach in analysis of protein-induced DNA bending is discussed.
引用
收藏
页码:111 / 121
页数:11
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