Published February 22, 2006 | Version v1
Journal article

On the physics of pressure denaturation of proteins

  • 1. Institute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011 (Japan)

Description

We show that the entropic effect originating from the translational movement of water molecules plays critical roles in the pressure-induced denaturation of proteins. In our statistical-mechanical method, the partial molar volume governing the pressure dependence of the structural stability is expressed in terms of the two geometric measures of each protein structure, the excluded volume and the accessible surface area for water molecules, and a parameter related to the water-density profile entropically formed near its surface. An unfolded structure, which is shown to turn more stable than the native one at an elevated pressure, successfully features the experimentally observed denaturation. (letter to the editor)

Availability note (English)

Available online at http://stacks.iop.org/0953-8984/18/L107/cm6_7_L01.pdf or at the Web site for the Journal of Physics. Condensed Matter (ISSN 1361-648X) http://www.iop.org/

Additional details

Publishing Information

Journal Title
Journal of Physics. Condensed Matter
Journal Volume
18
Journal Issue
7
Journal Page Range
p. L107-L113
ISSN
0953-8984
CODEN
JCOMEL

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
37061363
Subject category
S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
Descriptors DEI
DENSITY; MOLECULES; PARTIAL MOLAL VOLUME; PHASE STABILITY; PRESSURE DEPENDENCE; PROTEIN STRUCTURE; PROTEINS; SURFACE AREA; SURFACES; WATER
Descriptors DEC
HYDROGEN COMPOUNDS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PHYSICAL PROPERTIES; STABILITY; SURFACE PROPERTIES