| Literature DB >> 26282040 |
Lucia Comez1,2, Laura Lupi1,2, Assunta Morresi1,2, Marco Paolantoni1,2, Paola Sassi1,2, Daniele Fioretto1,2.
Abstract
Biological interfaces characterized by a complex mixture of hydrophobic, hydrophilic, or charged moieties interfere with the cooperative rearrangement of the hydrogen-bond network of water. In the present study, this solute-induced dynamical perturbation is investigated by extended frequency range depolarized light scattering experiments on an aqueous solution of a variety of systems of different nature and complexity such as small hydrophobic and hydrophilic molecules, amino acids, dipeptides, and proteins. Our results suggest that a reductionist approach is not adequate to describe the rearrangement of hydration water because a significant increase of the dynamical retardation and extension of the perturbation occurs when increasing the chemical complexity of the solute.Entities:
Keywords: H-bond network; biological interfaces; biological water; depolarized light scattering; hydration water; water diffusion
Year: 2013 PMID: 26282040 DOI: 10.1021/jz400360v
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475