• DocumentCode
    3087946
  • Title

    Improved LogitBoost Classifier Based Prediction of GPCR-G-Protein Coupling with Self-Adaptive Immune Algorithm

  • Author

    Gu, Quan ; Ding, Yong-Sheng

  • Author_Institution
    Coll. of Inf. Sci. & Technol., Donghua Univ., Shanghai, China
  • fYear
    2010
  • fDate
    18-20 June 2010
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    G-Protein coupled receptors (GPCRs) constitute the largest group of membrane receptors with great pharmacological interest. The signal transduction within cells is leaded by a wide range of native ligands interact and activate GPCRs. Most of these responses are mediated through the interaction of GPCRs with coupling GTP-binding proteins (G-proteins). For the reason of the information explosion in biological sequence databases, the development of software algorithms that could predict properties of GPCRs is important. In this paper, we have developed an intensive exploratory approach to predict the coupling preference of GPCRs to heterotrimeric G-proteins. An integrated recognition method combined with Self-Adaptive Immune Algorithm and LogitBoost classifier has been applied in prediction. The result indicates that the proposed method might become a potentially useful tool for GPCR-G-protein coupling prediction, or play a complimentary role to the existing methods in the relevant areas. The method predicts the coupling preferences of GPCRs to three kinds of G-protein subclasses, Gs, Gi/o and Gq/11, but not G12/13 for the limited amount.
  • Keywords
    bioinformatics; biomembranes; cellular transport; data handling; molecular biophysics; pattern classification; proteins; G-Protein coupled receptors; Gi/o G-protein subclass; Gq/11 G-protein subclass; Gs G-protein subclass; GPCR-G-protein coupling; GTP binding proteins; LogitBoost classifier based prediction; biological sequence databases; cell signal transduction; heterotrimeric G-proteins; integrated recognition; ligand-GPCR interaction; membrane receptors; native ligands; pharmacology; self adaptive immune algorithm; software algorithms; Bioinformatics; Biomembranes; Drugs; Educational institutions; Educational programs; Educational technology; Hidden Markov models; Immune system; Proteins; Textile technology;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
  • Conference_Location
    Chengdu
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-4712-1
  • Electronic_ISBN
    2151-7614
  • Type

    conf

  • DOI
    10.1109/ICBBE.2010.5514858
  • Filename
    5514858