posted on 2016-03-02, 00:00authored bySuman Saurabh, Matthew
A. Glaser, Yves Lansac, Prabal K. Maiti
We
report the first atomistic simulation of two stacked nucleosome
core particles (NCPs), with an aim to understand, in molecular detail,
how they interact, the effect of salt concentration, and how different
histone tails contribute to their interaction, with a special emphasis
on the H4 tail, known to have the largest stabilizing effect on the
NCP–NCP interaction. We do not observe specific K16-mediated
interaction between the H4 tail and the H2A–H2B acidic patch,
in contrast with the findings from crystallographic studies, but find
that the stacking was stable even in the absence of this interaction.
We perform simulations with the H4 tail (partially/completely) removed
and find that the region between LYS-16 and LYS-20 of the H4 tail
holds special importance in mediating the inter-NCP interaction. Performing
similar tail-clipped simulations with the H3 tail removed, we compare
the roles of the H3 and H4 tails in maintaining the stacking. We discuss
the relevance of our simulation results to the bilayer and other liquid-crystalline
phases exhibited by NCPs in vitro and, through an analysis of the
histone–histone interface, identify the interactions that could
possibly stabilize the inter-NCP interaction in these columnar mesophases.
Through the mechanical disruption of the stacked nucleosome system
using steered molecular dynamics, we quantify the strength of inter-NCP
stacking in the presence and absence of salt. We disrupt the stacking
at some specific sites of internucleosomal tail-DNA contact and perform
a comparative quantification of the binding strengths of various tails
in stabilizing the stacking. We also examine how hydrophobic interactions
may contribute to the overall stability of the stacking and find a
marked difference in the role of hydrophobic forces as compared with
electrostatic forces in determining the stability of the stacked nucleosome
system.