Evaluating cholinesterases inhibition by BAC and DDAC biocides: A combined experimental and theoretical approach
Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have b...
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Published in | Biochimica et biophysica acta. Biomembranes Vol. 1868; no. 12; p. 130726 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.12.2024
Elsevier |
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ISSN | 0304-4165 1872-8006 0005-2736 1872-8006 1879-2642 |
DOI | 10.1016/j.bbagen.2024.130726 |
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Abstract | Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases.
•A rapid colorimetric microplate test was developed to study cholinesterase inhibition by quaternary ammonium biocides.•4 different enzymes were tested including 3 acetylcholinesterases and 1 butyrylcholinesterase.•In silico molecular docking allowed confirmation of the results obtained by enzymatic methods. |
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AbstractList | Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases. Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases.Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases. Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases. •A rapid colorimetric microplate test was developed to study cholinesterase inhibition by quaternary ammonium biocides.•4 different enzymes were tested including 3 acetylcholinesterases and 1 butyrylcholinesterase.•In silico molecular docking allowed confirmation of the results obtained by enzymatic methods. |
ArticleNumber | 130726 |
Author | André, Isabelle Mouawad, Lynn Esque, Jeremy Noguer, Thierry Catanante, Gaëlle Istamboulie, Georges |
Author_xml | – sequence: 1 givenname: Lynn surname: Mouawad fullname: Mouawad, Lynn organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France – sequence: 2 givenname: Jeremy surname: Esque fullname: Esque, Jeremy organization: Toulouse Biotechnology Institute, TBI, Université de Toulouse, CNRS, INRAE, INSA, 31077 Toulouse, France – sequence: 3 givenname: Isabelle surname: André fullname: André, Isabelle organization: Toulouse Biotechnology Institute, TBI, Université de Toulouse, CNRS, INRAE, INSA, 31077 Toulouse, France – sequence: 4 givenname: Georges surname: Istamboulie fullname: Istamboulie, Georges organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France – sequence: 5 givenname: Gaëlle surname: Catanante fullname: Catanante, Gaëlle email: gaelle.catanante@univ-perp.fr organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France – sequence: 6 givenname: Thierry surname: Noguer fullname: Noguer, Thierry email: noguer@univ-perp.fr organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France |
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Keywords | Enzyme kinetics Biocides Molecular docking Cholinesterases molecular docking biocides enzyme kinetics |
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SubjectTerms | Acetylcholinesterase - metabolism Animals Benzalkonium Compounds - chemistry Benzalkonium Compounds - pharmacology Biochemistry, Molecular Biology Biocides Butyrylcholinesterase - chemistry Butyrylcholinesterase - metabolism Cattle Cholinesterase Inhibitors - chemistry Cholinesterase Inhibitors - pharmacology Cholinesterases Disinfectants - pharmacology Drosophila melanogaster - drug effects Drosophila melanogaster - enzymology Electrophorus Enzyme kinetics Erythrocytes - drug effects Erythrocytes - enzymology Horses Life Sciences Molecular docking Molecular Docking Simulation Quaternary Ammonium Compounds - chemistry Quaternary Ammonium Compounds - pharmacology |
Title | Evaluating cholinesterases inhibition by BAC and DDAC biocides: A combined experimental and theoretical approach |
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