Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy

Nucleus. 2020 Dec;11(1):264-282. doi: 10.1080/19491034.2020.1816053.

Abstract

The interplay between transcription factors, chromatin remodelers, 3-D organization, and mechanical properties of the chromatin fiber controls genome function in eukaryotes. Besides the canonical histones which fold the bulk of the chromatin into nucleosomes, histone variants create distinctive chromatin domains that are thought to regulate transcription, replication, DNA damage repair, and faithful chromosome segregation. Whether histone variants translate distinctive biochemical or biophysical properties to their associated chromatin structures, and whether these properties impact chromatin dynamics as the genome undergoes a multitude of transactions, is an important question in biology. Here, we describe single-molecule nanoindentation tools that we developed specifically to determine the mechanical properties of histone variant nucleosomes and their complexes. These methods join an array of cutting-edge new methods that further our quantitative understanding of the response of chromatin to intrinsic and extrinsic forces which act upon it during biological transactions in the nucleus.

Keywords: Chromatin; elasticity; epigenetics; nanoindentation force spectroscopy; nucleosomes.

Publication types

  • Research Support, N.I.H., Intramural
  • Video-Audio Media

MeSH terms

  • Chromatin Assembly and Disassembly*
  • HeLa Cells
  • Histones / chemistry*
  • Histones / metabolism
  • Histones / ultrastructure
  • Humans
  • Nucleosomes / chemistry*
  • Nucleosomes / metabolism
  • Nucleosomes / ultrastructure
  • Spectrum Analysis

Substances

  • Histones
  • Nucleosomes

Grants and funding

This work was supported by the National Cancer Institute [Intramural Research] and NIBIB [Intramural Research].