Published June 1, 2011 | Version v1
Journal article

The diversity of physical forces and mechanisms in intermolecular interactions

  • 1. Computational Biology Unit, Bergen Center for Computational Science, University of Bergen, 5008 Bergen (Norway)

Description

Intermolecular interactions became an inherent part of the structure–function paradigm. Therefore, the generalized concept of protein stability and interactions should consider the balance of stabilizing forces working in different types of intermolecular interactions. We consider here two 'extremes' of protein interactions, viral protein with high intrinsic disorder and hyperthermostable protein complexes. Intermolecular interactions provide folding upon binding as a part of function in the viral case, while they secure and stabilize specific native interfaces as a prerequisite for function in hyperthermostable complexes. We propose a generalized concept of protein stability and interactions, which includes intermolecular interactions comprising distinct combinations of stabilizing forces depending on the types of interacting partners

Availability note (English)

Available from http://dx.doi.org/10.1088/1478-3975/8/3/035002

Additional details

Identifiers

DOI
10.1088/1478-3975/8/3/035002;
PII
S1478-3975(11)72612-1;

Publishing Information

Journal Title
Physical Biology (Online)
Journal Volume
8
Journal Issue
3
Journal Page Range
[11 p.]
ISSN
1478-3975

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47032632
Subject category
S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
Descriptors DEI
BALANCES; COMPLEXES; FUNCTIONS; INTERACTIONS; INTERFACES; PROTEINS; STABILITY
Descriptors DEC
MEASURING INSTRUMENTS; ORGANIC COMPOUNDS; WEIGHT INDICATORS