Unique insight into protein-DNA interactions from single molecule atomic force microscopy

被引:5
|
作者
Bangalore, Disha Mohan [1 ]
Tessmer, Ingrid [1 ]
机构
[1] Rudolf Virchow Ctr Expt Biomed, Josef Schneider Str 2, D-97080 Wurzburg, Germany
来源
AIMS BIOPHYSICS | 2018年 / 5卷 / 03期
关键词
atomic force microscopy (AFM); protein-DNA interactions; single molecule methods;
D O I
10.3934/biophy.2018.3.194
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Protein-DNA interactions are pivotal for many essential biological processes. Atomic force microscopy (AFM) imaging of protein-DNA systems involved in DNA target site search, identification, and processing by proteins has contributed invaluable information to our understanding of the underlying mechanisms. The single molecule 3D resolution of AFM enables us to uncover stoichiometries and conformational properties of protein-DNA complexes. Its molecular resolution places AFM at the interface between the atomic resolution achievable by crystallography and the comparably poor (typically > hundred nanometers) spatial resolution of optical microscopy. Furthermore, the transient character of protein interactions with nonspecific DNA sites, for example during their target site search renders these complexes difficult to resolve by standard ensemble methods. Here, we review current applications and capabilities of as well as novel advances in AFM imaging in protein-DNA interaction studies.
引用
收藏
页码:194 / 216
页数:23
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