• Title of article

    Interaction of methotrexate with trypsin analyzed by spectroscopic and molecular modeling methods

  • Author/Authors

    Wang، نويسنده , , Yanqing and Zhang، نويسنده , , Hongmei and Cao، نويسنده , , Jian and Zhou، نويسنده , , Qiuhua، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2013
  • Pages
    8
  • From page
    78
  • To page
    85
  • Abstract
    Trypsin is one of important digestive enzymes that have intimate correlation with human health and illness. In this work, the interaction of trypsin with methotrexate was investigated by spectroscopic and molecular modeling methods. The results revealed that methotrexate could interact with trypsin with about one binding site. Methotrexate molecule could enter into the primary substrate-binding pocket, resulting in inhibition of trypsin activity. Furthermore, the thermodynamic analysis implied that electrostatic force, hydrogen bonding, van der Waals and hydrophobic interactions were the main interactions for stabilizing the trypsin–methotrexate system, which agreed well with the results from the molecular modeling study.
  • Keywords
    Methotrexate , Trypsin , Activity inhibition , Spectroscopy , molecular modeling
  • Journal title
    Journal of Molecular Structure
  • Serial Year
    2013
  • Journal title
    Journal of Molecular Structure
  • Record number

    1974745