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Title: Computational investigation of the HIV-1 Rev multimerization using molecular dynamics simulations and binding free energy calculations
Authors: Venken, Tom
Daelemans, Dirk
De Maeyer, Marc ×
Voet, Arnout #
Issue Date: Mar-2012
Publisher: John Wiley & Sons
Series Title: Proteins: Structure, Function and Genetics vol:80 pages:1633-1646
Article number: 10.1002/prot.24057
Abstract: The HIV Rev protein mediates the nuclear export of viral mRNA, and is thereby essential for the production of late viral proteins in the replication cycle. Rev forms a large organized multimeric protein-protein complex for proper functioning. Recently, the three-dimensional structures of a Rev dimer and tetramer have been resolved and provide the basis for a thorough structural analysis of the binding interaction. Here, molecular dynamics (MD) and binding free energy calculations were performed to elucidate the forces thriving dimerization and higher order multimerization of the Rev protein. It is found that despite the structural differences between each crystal structure, both display a similar behavior according to our calculations. Our analysis based on a molecular mechanics-generalized Born surface area (MM/GBSA) and a configurational entropy approach demonstrates that the higher order multimerization site is much weaker than the dimerization site. In addition, a quantitative hot spot analysis combined with a mutational analysis reveals the most contributing amino acid residues for protein interactions in agreement with experimental results. Additional residues were found in each interface, which are important for the protein interaction. The investigation of the thermodynamics of the Rev multimerization interactions performed here could be a further step in the development of novel antiretrovirals using structure based drug design. Moreover, the variability of the angle between each Rev monomer as measured during the MD simulations suggests a role of the Rev protein in allowing flexibility of the arginine rich domain (ARM) to accommodate RNA binding. Proteins 2012; © 2012 Wiley Periodicals, Inc.
URI: 
ISSN: 0887-3585
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Biochemistry, Molecular and Structural Biology Section
Laboratory of Virology and Chemotherapy (Rega Institute)
× corresponding author
# (joint) last author

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