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Related Concept Videos

Atomic Force Microscopy01:08

Atomic Force Microscopy

Atomic force microscopy (AFM) is a type of scanning probe microscopy that can analyze topographic details of various specimens like ceramics, glass, polymers, and biological samples. AFM offers over 1000 times more resolution than the optical imaging system. Images generated from AFM are three-dimensional surface profiles, offering an advantage over the flat, two-dimensional images from other imaging techniques.
The AFM Probe
The probe is regarded as the heart of any AFM setup and comprises the...
Nucleosome Remodeling02:54

Nucleosome Remodeling

Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
Studying the Cytoskeleton01:17

Studying the Cytoskeleton

The cytoskeletal architecture can be studied using different microscopic and biochemical techniques. Electron microscopy was instrumental in discovering the cytoskeletal architecture around the 1960s, which allowed obtaining structural information at a high-resolution level. However, the sample preparation procedure often limits this ability in biological samples. Several protocols have been developed over the years to optimize sample preparation. In one of the protocols known as rotary...
Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer is an enzyme that can...

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Related Experiment Video

Updated: Jul 16, 2026

Probing The Structure And Dynamics Of Nucleosomes Using Atomic Force Microscopy Imaging
09:52

Probing The Structure And Dynamics Of Nucleosomes Using Atomic Force Microscopy Imaging

Published on: January 31, 2019

Using atomic force microscopy to study chromatin structure and nucleosome remodeling.

D Lohr1, R Bash, H Wang

  • 1Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287-1604, USA. dlohr@asu.edu

Methods (San Diego, Calif.)
|February 21, 2007
PubMed
Summary

Atomic force microscopy (AFM) allows direct imaging of single molecules in solution. This study adapted AFM techniques to analyze nucleosome arrays, revealing insights into their structure and remodeling by the Swi-Snf complex.

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Last Updated: Jul 16, 2026

Probing The Structure And Dynamics Of Nucleosomes Using Atomic Force Microscopy Imaging
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Published on: January 31, 2019

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Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA
10:40

Assembly of Nucleosomal Arrays from Recombinant Core Histones and Nucleosome Positioning DNA

Published on: September 10, 2013

Area of Science:

  • Biophysics
  • Molecular Biology
  • Microscopy

Background:

  • Atomic force microscopy (AFM) offers direct visualization of single molecules in solution.
  • Understanding nucleosome array properties is crucial for comprehending DNA packaging and regulation.

Purpose of the Study:

  • To adapt AFM methods for detailed analysis of nucleosome arrays.
  • To investigate nucleosome features like DNA-histone binding, stability, and the impact of acetylation.
  • To track nucleosome remodeling by the human Swi-Snf complex.

Main Methods:

  • Utilized specialized AFM techniques for repetitive imaging in liquid.
  • Adapted environmental control for samples during imaging.
  • Developed methods for identifying specific molecules in complex samples.

Main Results:

  • Successfully analyzed DNA-histone binding strength and nucleosome stability in arrays.
  • Compared nucleosome features across different array types.
  • Monitored the dynamic response of nucleosomes to Swi-Snf remodeling.

Conclusions:

  • Advanced AFM methodologies enable in-depth studies of nucleosome array dynamics.
  • These techniques provide unique insights into chromatin structure and remodeling processes.
  • The study highlights AFM's power in investigating biological material properties and functions.