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Tension-Dependent Free Energies of Nucleosome Unwrapping
Journal article   Open access

Tension-Dependent Free Energies of Nucleosome Unwrapping

Joshua Lequieu, Andres Cordoba, David C. Schwartz, Juan J. de Pablo and Argonne National Laboratory (ANL), Argonne, IL (United States)
ACS central science, v 2(9), pp 660-666
28 Sep 2016
PMID: 27725965
url
https://doi.org/10.1021/acscentsci.6b00201View
Published, Version of Record (VoR) Open

Abstract

Chemistry Chemistry, Multidisciplinary Physical Sciences Science & Technology
Nucleosomes form the basic unit of compaction within eukaryotic genomes, and their locations represent an important, yet poorly understood, mechanism of genetic regulation. Quantifying the strength of interactions within the nucleosome is a central problem in biophysics and is critical to understanding how nucleosome positions influence gene expression. By comparing to single-molecule experiments, we demonstrate that a coarse-grained molecular model of the nucleosome can reproduce key aspects of nucleosome unwrapping. Using detailed simulations of DNA and histone proteins, we calculate the tension-dependent free energy surface corresponding to the unwrapping process. The model reproduces quantitatively the forces required to unwrap the nucleosome and reveals the role played by electrostatic interactions during this process. We then demonstrate that histone modifications and DNA sequence can have significant effects on the energies of nucleosome formation. Most notably, we show that histone tails contribute asymmetrically to the stability of the outer and inner turn of nucleosomal DNA and that depending on which histone tails are modified, the tension-dependent response is modulated differently.

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Collaboration types
Domestic collaboration
Web of Science research areas
Chemistry, Multidisciplinary
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