DocumentCode :
2691686
Title :
Rotation crossover and K-site move mutation for evolutionary protein folding in 3D FCC HP model (preliminary version)
Author :
Su, Shih-Chieh ; Tsay, Jyh-Jong
Author_Institution :
Dept. of Comput. Sci. & Inf. Eng., Nat. Chung Cheng Univ., Chiavi, Taiwan
fYear :
2012
fDate :
4-7 Oct. 2012
Firstpage :
1
Lastpage :
4
Abstract :
In this paper we present a new evolutionary algorithm for the protein folding problem. We study the problem in the 3D FCC HP model which has been widely used in previous research. Our focus is to develop evolutionary algorithms (EA) which are robust, easy to operate and can handle various energy functions. We propose lattice rotation for crossover and K-site move for mutation, which form the key components of our evolutionary algorithms. Experiment shows that our algorithms are able to find minimum-energy conformations for many sequences whose optimal conformations are not found in previous EA-based algorithms. Furthermore, our idea can be easily integrated into Monte Carlo and Tabu searches as approaches for local searches.
Keywords :
Monte Carlo methods; bioinformatics; biological techniques; evolutionary computation; molecular biophysics; proteins; 3D FCC HP model; Monte Carlo search; Tabu search; energy functions; evolutionary algorithm; evolutionary protein folding; k-site move mutation; lattice rotation; minimum energy conformations; protein sequences; rotation crossover; Biological system modeling; Computational modeling; FCC; Lattices; Protein engineering; Proteins; Solid modeling; 3D FCC Model; Evolutionary Algorithms; HP Model; Protein Structure Prediction;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Bioinformatics and Biomedicine (BIBM), 2012 IEEE International Conference on
Conference_Location :
Philadelphia, PA
Print_ISBN :
978-1-4673-2559-2
Electronic_ISBN :
978-1-4673-2558-5
Type :
conf
DOI :
10.1109/BIBM.2012.6392715
Filename :
6392715
Link To Document :
بازگشت