Comparative bioinformatics analysis of prion proteins isolated from reptile, rodent, ruminant, and human species.
- Author:
Insung AHN
1
;
Hyeon Seok SON
Author Information
1. Bioinformatics Team, Supercomputing Center, Korea Institute of Science and Technology Information, Daejeon 305-806, Korea.
- Publication Type:Original Article ; Comparative Study ; Research Support, Non-U.S. Gov't
- Keywords:
computational biology;
neurodegenerative diseases;
phylogeny;
prions;
proteomics
- MeSH:
Animals;
Cattle;
*Computational Biology;
Humans;
Phylogeny;
Prions/*chemistry/classification/*genetics/isolation & purification;
Reptiles/metabolism;
Rodentia/metabolism;
Ruminants/metabolism;
Sequence Analysis, Protein;
Species Specificity
- From:Experimental & Molecular Medicine
2007;39(6):769-777
- CountryRepublic of Korea
- Language:English
-
Abstract:
Prion proteins (PrPs) are infectious pathogens that cause a group of invariably fatal, neurodegenerative diseases, including Creutzfeldt-Jakob disease, by means of an entirely novel mechanism. They are produced by various species, including reptile, rodent, ruminant and mammals, during normal metabolic processes, but they can be slowly changed into pathogenic isoforms upon contact with other infectious PrP isoforms. This transmission can occur across species barriers. In the present study, phylogram for each PrP sequence was generated by PAUP* 4.0 program using Neighbor-Joining method with 1,000 times bootstrapping process for the phylogenetic analysis. The molecular dynamics (MD) simulations were performed by the SANDER module in the AMBER 7 package using Amber 99 force field. All the simulation process was conducted in the IBM p690 Supercomputing System in Korea Institute of Science and Technology Information. To reduce the calculation time, we used the Generalized Born (GB) model. We compared the sequences and structural characteristics of normal and pathogenic (E200K) human PrPs with those of other reptile, rodent, ruminant and mammalian PrPs. Phylogenetic analysis revealed that, although the turtle PrP sequence is the most distinct of the PrPs analyzed, it nonetheless retains five conserved secondary structural elements that are similar to those found in the mammalian PrPs, suggesting that these elements have important functions in vivo. The RMS deviation between the normal and E200K human PrPs was larger than that between the normal human and bovine PrPs, and all of the beta-sheet structures in human E200K PrP were very stable during MD simulations.
