Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7810027 | Journal of Molecular Structure | 2013 | 8 Pages |
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.
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Authors
Yanqing Wang, Hongmei Zhang, Jian Cao, Qiuhua Zhou,