• DocumentCode
    2497668
  • Title

    An Efficient Hardware-Based Approach for Molecular Folding Calculations via System-on-Chip

  • Author

    Sung, Wen-Tsai

  • Author_Institution
    Dept. of Electr. Eng., Nat. Chin-Yi Univ. of Technol., Taiping, Taiwan
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    This paper presents a methodology for the design of a reconfigurable computing system applied to a complex problem in molecular Biology: the protein folding problem. This paper employed VMD tool and force field simulation theorem based on FPGA for protein folding solution. This technique consists of two components: finished protein folding process and found out active sites for drug docking. The goal of protein folding simulation is to search the global energy minimum location with stability state and the when the protein is finished the folding task, we can find out the active sites for pre-process of ligand protein docking. An efficient hardware-based approach was devised to achieve a significant reduction of the search space of possible foldings. Several simulations were done to evaluate the performance of the system as well as the demand for FPGA´s resources.
  • Keywords
    biology computing; drugs; field programmable gate arrays; molecular biophysics; molecular configurations; proteins; reconfigurable architectures; system-on-chip; FPGA; VMD tool; active sites; drug docking; force field simulation theorem; global energy minimum location; hardware-based approach; molecular biology; molecular folding calculation; protein folding; reconfigurable computing system; system-on-chip; Alzheimer´s disease; Biological system modeling; Biology computing; Computational modeling; Computer simulation; Drugs; Field programmable gate arrays; Nanobioscience; Proteins; System-on-a-chip;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5162315
  • Filename
    5162315