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
Link To Document :
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