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

Journal

AIMS BIOPHYSICS
Volume 5, Issue 3, Pages 194-216

Publisher

AMER INST MATHEMATICAL SCIENCES-AIMS
DOI: 10.3934/biophy.2018.3.194

Keywords

atomic force microscopy (AFM); protein-DNA interactions; single molecule methods

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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.

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