MP2//DFT calculations of interaction energies between acetaminophen and acetaminophen analogues and the aryl sulfotransferase active site

作者：DiGiovanni Katherine M; Hatstat A Katherine; Rote Jennifer; Cafiero Mauricio^*

来源：Computational and Theoretical Chemistry, 2013, 1007: 41-47.

DOI：10.1016/j.comptc.2012.12.004

• Sulfotransferase
• Acetaminophen
• DFT
• MP2
• Hydrogen-bonds

Paracetamol, or acetaminophen, is a commonly used analgesic and antipyretic. Cresols such as p-cresol, o-cresol, and m-cresol can compete with acetaminophen for metabolism via several pathways, including via sulfation by aryl sulfotransferase. We have applied the MP2 method to study the interaction of acetaminophen and these cresol analogues with the active site of aryl sulfotransferase. Docking and BHandH-LYP/6-31G optimization were used to find the structures of the ligand-protein complexes assuming a static active site. Interaction energies between the ligands and each of the amino acids in the active site were calculated using MP2 with a basis set of 6-311+g*. Further optimizations were then performed to allow flexibility of the amino acid residue side-chains in the active site and interaction energies were calculated for these complexes as well. p-Cresol is shown to compete with acetaminophen for this metabolic pathway, in agreement with experiment. We also show that m-cresol should be competitive for this metabolic pathway.

• 出版日期2013-3-1