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Novel activity of human BChE: Lipid hydrolysis

dc.contributor.authorGok, Muslum
dc.contributor.authorCicek, Cigdem
dc.contributor.authorSari, Suat
dc.contributor.authorBodur, Ebru
dc.date.accessioned2026-10-09T21:47:50Z
dc.date.issued2023
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstractAcetylcholinesterase and butyrylcholinesterase (BChE) typically hydrolyze the neurotransmitter acetylcholine. The multifunctional enzyme BChE is associated with lipid metabolism through an undefined mechanism. Based on lipid-related studies and by comparing the structural similarities between lipases and BChE we postulated that the association of BChE with lipid metabolism could occur through hydrolytic activity. Utilizing purified BChE enzymes from different sources and several lipases as controls, the ability of BChE to hydrolyze 4-methylumbelliferyl (4-mu) palmitate is investigated. Using lectin affinity, inhibition kinetics, and molecular modeling, we demonstrated that purified BChE hydrolyzed 4mu palmitate at pH 8 as effectively as wheat germ lipase. The affinity Km value of the enzymes for 4mu palmitate as substrate is found as 10.4 mu M, 34.2 mu M, 129.8 mu M, and 186 mu M for wheat germ lipase, purified BChE, pancreatic lipase, and commercial BChE, respectively. Analysis of the inhibitory effect of 4mu palmitate on BChE using butyrylthiocholine as substrate revealed competitive inhibition with Ki and IC50 values of 448 mu M and 987.2 mu M, respectively. The binding affinity and interactions of 4-mu palmitate with BChE and pancreatic lipase were predicted by molecular docking. These results suggest that BChE possesses lipolytic activity. The possibility that BChE hydrolyzes not only 4-mu palmitate but also other types of lipids will lead to a new approach to those disease states associated with increased BChE activity/expression.(c) 2022 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.
dc.description.sponsorshipHacettepe University [TDK-2018-17028]; International Research Fellowship Program [TUBITAK 2214-A]
dc.description.sponsorshipThis work was funded from Hacettepe University Grant No: TDK-2018-17028 to E.B and by TUBITAK 2214-A International Research Fellowship Program to M.G.
dc.identifier.doi10.1016/j.biochi.2022.09.008
dc.identifier.endpage135
dc.identifier.issn0300-9084
dc.identifier.issn1638-6183
dc.identifier.orcid0000-0003-2875-291X
dc.identifier.orcid0000-0001-5829-5487
dc.identifier.orcid0000-0001-5481-4438
dc.identifier.orcid0000-0002-8248-4218
dc.identifier.pmid36126749
dc.identifier.scopus2-s2.0-85139226854
dc.identifier.scopusqualityQ2
dc.identifier.startpage127
dc.identifier.urihttps://doi.org/10.1016/j.biochi.2022.09.008
dc.identifier.urihttps://hdl.handle.net/20.500.12794/3495
dc.identifier.volume204
dc.identifier.wosWOS:000919563300001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynak.digerScience Citation Index Expanded (SCI-EXPANDED)
dc.language.isoen
dc.publisherElsevier France-Editions Scientifiques Medicales Elsevier
dc.relation.ispartofBiochimie
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.sdgGoal-03: Good Health and Well-Being
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260922
dc.subjectButyrylcholinesterase
dc.subjectLipid Hydrolysis
dc.subject4-Mu Palmitate
dc.subjectMolecular Docking
dc.subjectEnzyme Kinetics
dc.subjectMultifunctionality
dc.titleNovel activity of human BChE: Lipid hydrolysis
dc.typeArticle

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