Hydrogen bond breaking mechanism and water reorientational dynamics in the hydration layer of lysozyme

Jana, Biman ; Pal, Subrata ; Bagchi, Biman (2008) Hydrogen bond breaking mechanism and water reorientational dynamics in the hydration layer of lysozyme Journal of Physical Chemistry B, 112 (30). pp. 9112-9117. ISSN 1089-5647

Full text not available from this repository.

Official URL: http://pubs.acs.org/doi/abs/10.1021/jp800998w

Related URL: http://dx.doi.org/10.1021/jp800998w


The mechanism and the rate of hydrogen bond-breaking in the hydration layer surrounding an aqueous protein are important ingredients required to understand the various aspects of protein dynamics, its function, and stability. Here, we use computer simulation and a time correlation function technique to understand these aspects in the hydration layer of lysozyme. Water molecules in the layer are found to exhibit three distinct bond-breaking mechanisms. A large angle orientational jump of the donor water molecule is common among all of them. In the most common (≈80%) bond-breaking event in the layer, the new acceptor water molecule comes from the first coordination shell (initially within 3.5 Å of the donor), and the old acceptor water molecule remains within the first coordination shell, even after the bond-breaking. This is in contrast to that in bulk water, in which both of the acceptor molecules involve the second coordination shell. Additionally, the motion of the incoming and the outgoing acceptor molecules involved is not diffusive in the hydration layer, in contrast to their observed diffusive motion in the bulk. The difference in rotational dynamics between the bulk and the hydration layer water molecules is clearly manifested in the calculated time-dependent angular van Hove self-correlation function (G(θ, t)) which has a pronounced two-peak structure in the layer, and this can be traced to the constrained translational motion in the layer. The longevity of the surrounding hydrogen bond network is found to be significantly enhanced near a hydrophilic residue.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:4005
Deposited On:13 Oct 2010 07:02
Last Modified:07 Jan 2011 06:23

Repository Staff Only: item control page