Change in a protein's electronic structure induced by an explicit solvent : an ab initio fragment molecular orbital study of ubiquitin

(c) 2007 Wiley Periodicals, Inc.

Bibliographische Detailangaben
Veröffentlicht in:Journal of computational chemistry. - 1984. - 28(2007), 10 vom: 30. Juli, Seite 1750-62
1. Verfasser: Komeiji, Yuto (VerfasserIn)
Weitere Verfasser: Ishida, Toyokazu, Fedorov, Dmitri G, Kitaura, Kazuo
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Journal of computational chemistry
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Solvents Ubiquitin
Beschreibung
Zusammenfassung:(c) 2007 Wiley Periodicals, Inc.
The effect of solvation on the electronic structure of the ubiquitin protein was analyzed using the ab initio fragment molecular orbital (FMO) method. FMO calculations were performed for the protein in vacuo, and the protein was immersed in an explicit solvent shell as thick as 12 A at the HF or MP2 level by using the 6-31G* basis set. The protein's physical properties examined were the net charge, the dipole moment, the internal energy, and the solvent interaction energy. Comparison of the computational results revealed the following changes in the protein upon solvation. First, the positively charged amino acid residues on the protein surface drew electrons from the solvent, while the negatively charged ones transfer electrons to the solvent. Second, the dipole moment of the protein was enhanced as a result of the polarization. Third, the internal energy of the protein was destabilized, but the destabilization was more than compensated for by the generation of a favorable protein-solvent interaction. Finally, the energetic changes were elicited both by the electron correlation effect of the first solvent shell and by the electrostatic effect of more distant solvent molecules. These findings were consistent with the picture of the solvated protein being a polarizable molecule dissolved in a dielectric media
Beschreibung:Date Completed 10.08.2007
Date Revised 29.05.2007
published: Print
Citation Status MEDLINE
ISSN:1096-987X