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Free Energy Profile of APOBEC3G Protein Calculated by a Molecular Dynamics Simulation.
Fukunishi, Yoshifumi; Hongo, Saki; Lintuluoto, Masami; Matsuo, Hiroshi.
Afiliación
  • Fukunishi Y; Biomedicinal Information Research Center (BIRC), National Institute of Advanced Industrial Science and Technology (AIST), 2-3-26, Aomi, Koto-ku, Tokyo 135-0064, Japan. y-fukunishi@aist.go.jp.
  • Hongo S; Division of Applied Life Science, Graduate School of Life and Environmental Science, Kyoto Prefectural University, Kyoto 606-8522, Japan. s_hongo@mei.kpu.ac.jp.
  • Lintuluoto M; Division of Applied Life Science, Graduate School of Life and Environmental Science, Kyoto Prefectural University, Kyoto 606-8522, Japan. masami@kpu.ac.jp.
  • Matsuo H; Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, MN 55455, USA. matsu029@umn.edu.
Biology (Basel) ; 1(2): 245-59, 2012 Jul 26.
Article en En | MEDLINE | ID: mdl-24832225
The human APOBEC3G protein (A3G) is a single-stranded DNA deaminase that inhibits the replication of retrotransposons and retroviruses, including HIV-1. Atomic details of A3G's catalytic mechanism have started to emerge, as the structure of its catalytic domain (A3Gctd) has been revealed by NMR and X-ray crystallography. The NMR and crystal structures are similar overall; however, differences are apparent for ß2 strand (ß2) and loops close to the catalytic site. To add some insight into these differences and to better characterize A3Gctd dynamics, we calculated its free energy profile by using the Generalized-Born surface area (GBSA) method accompanied with a molecular dynamics simulation. The GBSA method yielded an enthalpy term for A3Gctd's free energy, and we developed a new method that takes into account the distribution of the protein's dihedral angles to calculate its entropy term. The structure solved by NMR was found to have a lower energy than that of the crystal structure, suggesting that this conformation is dominant in solution. In addition, ß2-loop-ß2' configuration was stable throughout a 20-ns molecular dynamics (MD) simulation. This finding suggests that in solution A3Gctd is not likely to adopt the continuous ß2 strand configuration present in the APOBEC2 crystal structure. In the NMR structure, the solvent water accessibility of the catalytic Zn2+ was limited throughout the 20-ns MD simulation. This result explains previous observations in which A3G did not bind or catalyze single cytosine nucleotide, even when at excessive concentrations.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biology (Basel) Año: 2012 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biology (Basel) Año: 2012 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Suiza