4.7 Article

FRET-based methods to study ATP-dependent changes in chromatin structure

Journal

METHODS
Volume 41, Issue 3, Pages 291-295

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2006.08.015

Keywords

chromatin; ATP-dependent chromatin-remodeling; nucleosome; FRET; histone; real-time; SNF2h

Funding

  1. NIGMS NIH HHS [R01 GM073767] Funding Source: Medline
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM073767] Funding Source: NIH RePORTER

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DNA packaging into chromatin imposes several levels of regulation on the central nuclear processes of DNA replication, recombination, repair and transcription. ATP-dependent chromatin-remodeling enzymes play a critical role in this regulation by altering the accessibility of nucleosomal DNA. Remodeling can result in large-scale changes in chromatin, such as the formation of heterochromatin, or smaller changes in exposure or occlusion of specific DNA regions. To understand the mechanisms-of chromatin remodeling, we report a FRET-based method to follow remodeling of a single histone octamer on DNA. This technique provides a non-perturbing, solution-based approach to quantitatively track the movement of DNA with respect to the octamer in real-time. The method can easily be altered to examine other conformational changes within the nucleosome, and is applicable to study the enzymatic activity of several classes of chromatin-remodeling complexes. (c) 2006 Elsevier Inc. All rights reserved.

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