Molecular Dynamics Simulations of Acylpeptide Hydrolase Bound to Chlorpyrifosmethyl Oxon and Dichlorvos

International Journal of Molecular Sciences

Weiwei Han¹  Dongmei Wang¹  Hanyong Jin¹  Zhenhuan Zhou²  Shanshan Guan³ 

[1] Key Laboratory for Molecular Enzymology and Engineering of the Ministry of Education,College of Life Science, Jilin University, Changchun 130023, China;Second Bethune Hospital of Jilin University, Changchun 130041, China;State Key Laboratory of Theoretical and Computational Chemistry,Institute of Theoretical Chemistry, Jilin University, Changchun 130023, China;

关键词: acylpeptide hydrolase;    organophosphorus compound;    docking study;    molecular dynamics simulation;   

DOI  :  10.3390/ijms16036217

来源: DOAJ

【 摘 要 】

Acylpeptide hydrolases (APHs) catalyze the removal of N-acylated amino acids from blocked peptides. Like other prolyloligopeptidase (POP) family members, APHsare believed to be important targets for drug design. To date, the binding pose of organophosphorus (OP) compounds of APH, as well as the different OP compounds binding and inducing conformational changes in two domains, namely, α/β hydrolase andβ-propeller, remain poorly understood. We report a computational study of APH bound to chlorpyrifosmethyl oxon and dichlorvos. In our docking study, Val471 and Gly368 are important residues for chlorpyrifosmethyl oxon and dichlorvos binding. Molecular dynamics simulations were also performed to explore the conformational changes between the chlorpyrifosmethyl oxon and dichlorvos bound to APH, which indicated that the structural feature of chlorpyrifosmethyl oxon binding in APH permitted partial opening of theβ-propeller fold and allowed the chlorpyrifosmethyl oxon to easily enter the catalytic site. These results may facilitate the design of APH-targeting drugs with improved efficacy.

【 授权许可】

Unknown