Dynamics of Nucleosomal Structures Measured by High‐Speed Atomic Force Microscopy |
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| Authors: | Allard J. Katan Rifka Vlijm Alexandra Lusser Cees Dekker |
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| Affiliation: | 1. Bionanoscience Department, Kavli Institute of Nanoscience, Delft University of Technology, CJ, The Netherlands;2. Division of Molecular Biology, Innsbruck Medical University, Innsbruck, Austria |
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| Abstract: | The accessibility of DNA is determined by the number, position, and stability of nucleosomes, complexes consisting of a core of 8 histone proteins with DNA wrapped around it. Since the structure and dynamics of nucleosomes affects essential cellular processes, they are the subject of many current studies. Here, high‐speed atomic force microscopy is used to visualize dynamic processes in nucleosomes and tetrasomes (subnucleosomal structures that contain 4 rather than 8 histones in the protein core). Nucleosomes can spontaneously disassemble in a process (at a 1 second timescale). For tetrasomes, multiple dynamic phenomena are observed. For example, during disassembly the formation of a DNA loop (～25 nm in length) is seen, which remains stable for several minutes. For intact tetrasomes, dynamics in the form of sliding and reversible hopping between stable positions along the DNA are observed. The data emphasize that tetrasomes are not merely static objects but highly dynamic. Since tetrasomes (in contrast to nucleosomes) can stay on the DNA during transcription, the observed tetrasome dynamics is relevant for an understanding of the nucleosomal dynamics during transcription. These results illustrate the diversity of nucleosome dynamics and demonstrate the ability of high speed AFM to characterize protein‐DNA interactions. |
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| Keywords: | single‐molecule studies DNA atomic force microscopy nucleosome dynamics imaging |
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