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Bioimpacts. 2017;7(3): 147-153. doi: 10.15171/bi.2017.18
PMID: 29159142        PMCID: PMC5684506

Original Research

Investigation of the binding mechanism and inhibition of bovine liver catalase by quercetin: Multi-spectroscopic and computational study

Samaneh Rashtbari 1, Gholamreza Dehghan 1 * , Reza Yekta 1, Abolghasem Jouyban 2

Cited by CrossRef: 28

1- Hasković E, Herenda S, Halilović Z, Unčanin S, Hasković D, Deljkić E. Investigation of the Effect of Loratadine and Calcium Ions on Oxidoreductase Activity of Catalase Enzyme. CEI. 2021;17(1):26 [Crossref]
2- Mohd Bakhori N, Yusof N, Abdullah J, Wasoh H, Ab Rahman S, Abd Rahman S. Surface Enhanced CdSe/ZnS QD/SiNP Electrochemical Immunosensor for the Detection of Mycobacterium Tuberculosis by Combination of CFP10-ESAT6 for Better Diagnostic Specificity. Materials. 2019;13(1):149 [Crossref]
3- Nedić O, Penezić A, Minić S, Radomirović M, Nikolić M, Ćirković Veličković T, Gligorijević N. Food Antioxidants and Their Interaction with Human Proteins. Antioxidants. 2023;12(4):815 [Crossref]
4- Sistani P, Dehghan G, Sadeghi L. Structural and kinetic insights into HIV-1 reverse transcriptase inhibition by farnesiferol C. International Journal of Biological Macromolecules. 2021;174:309 [Crossref]
5- Yekta R, Dehghan G, Rashtbari S, Sadeghi L, Baradaran B, Sheibani N, Moosavi-Movahedi A. The impact of water molecules on binding affinity of the anti-diabetic thiazolidinediones for catalase: Kinetic and mechanistic approaches. Archives of Biochemistry and Biophysics. 2019;664:110 [Crossref]
6- Shahraki S, Delarami H, Razmara Z, Heidari A. Tracking the binding site of anticancer drug fluxoridin with Fe-related proteins to achieve intelligent drug delivery. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2024;306:123569 [Crossref]
7- Zhou L, Zhou H, Xiao H, Zhang Z, Xiong Z, Tuo X, Guo H. Elucidation on inhibition and binding mechanism of bovine liver catalase by nifedipine: multispectroscopic analysis and computer simulation methods. Luminescence. 2022;37(9):1547 [Crossref]
8- Panahi Y, Yekta R, Dehghan G, Rashtbari S, Baradaran B, Jafari N, Moosavi-Movahedi A. Aspirin in retrieving the inactivated catalase to active form: Displacement of one inhibitor with a protective agent. International Journal of Biological Macromolecules. 2019;122:306 [Crossref]
9- Rashtbari S, Dehghan G, Amini M, Khorram S, Khataee A. A sensitive colori/fluorimetric nanoprobe for detection of polyphenols using peroxidase-mimic plasma-modified MoO3 nanoparticles. Chemosphere. 2022;295:133747 [Crossref]
10- A. A. TRANSFER OF HUMAN HAIR EXOCUTICLES ONTO GLASS BY LIQUID CATALASE AND WHOLE BLOOD (REPORTING BLOOD CLUMPING FORMATION WHEN CONTACT WITH KERATIN AS POSSIBLE FACTOR IN ATHEROSCLEROSIS). Int J Res Granthaalayah. 2020;6(10):187 [Crossref]
11- Barreca D, Neri G, Scala A, Fazio E, Gentile D, Rescifina A, Piperno A. Covalently immobilized catalase on functionalized graphene: effect on the activity, immobilization efficiency, and tetramer stability. Biomater Sci. 2018;6(12):3231 [Crossref]
12- Lee S, Choi M, Al Adem K, Lukman S, Kim T. Aggregation and Cellular Toxicity of Pathogenic or Non-pathogenic Proteins. Sci Rep. 2020;10(1) [Crossref]
13- Khan J, Malik A, Rehman M, AlAjmi M, Ahmed M, Almutairi G, Anwer M, Khan R. Cationic gemini surfactant stimulates amyloid fibril formation in bovine liver catalase at physiological pH. A biophysical study. RSC Adv. 2020;10(71):43751 [Crossref]
14- Shahraki K, Shahraki S, Sori Nezami Z, Samareh Delarami H. New acetohydrazide-based Schiff base complexes with the ability to enhance catalase activity. Inorganic Chemistry Communications. 2024;163:112318 [Crossref]
15- Khataee S, Dehghan G, Yekta R, Rashtbari S, Maleki S, Khataee A. The protective effect of natural phenolic compound on the functional and structural responses of inhibited catalase by a common azo food dye. Food and Chemical Toxicology. 2022;160:112801 [Crossref]
16- Hanifeh Ahagh M, Dehghan G, Mahdavi M, Hosseinpour Feizi M, Teimuri-Mofrad R, Payami E, Mehdipour M, Rashtbari S. DNA binding ability and cytotoxicity, cell cycle arrest and apoptosis inducing properties of a benzochromene derivative against K562 human leukemia cells. Nucleosides, Nucleotides & Nucleic Acids. 2021;40(7):732 [Crossref]
17- Rashtbari S, Dehghan G, Sadeghi L, Sareminia L, Iranshahy M, Iranshahi M, Khataee A, Yoon Y. Interaction of bovine serum albumin with ellagic acid and urolithins A and B: Insights from surface plasmon resonance, fluorescence, and molecular docking techniques. Food and Chemical Toxicology. 2022;162:112913 [Crossref]
18- Shaghaghi M, Dehghan G, Rashtbari S, Sheibani N, Aghamohammadi A. Multispectral and computational probing of the interactions between sitagliptin and serum albumin. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2019;223:117286 [Crossref]
19- Maleki S, Dehghan G, Sadeghi L, Rashtbari S, Iranshahi M, Sheibani N. Surface plasmon resonance, fluorescence, and molecular docking studies of bovine serum albumin interactions with natural coumarin diversin. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2020;230:118063 [Crossref]
20- Samal R, Kumari K, Sahoo Y, Mishra S, Subudhi U. Interaction of artemisinin protects the activity of antioxidant enzyme catalase: A biophysical study. International Journal of Biological Macromolecules. 2021;172:418 [Crossref]
21- Shaghaghi M, Rashtbari S, Abdollahi A, Dehghan G, Jouyban A. A Sensitive, Simple and Direct Determination of Pantoprazole Based on a “Turn off-on” Fluorescence Nanosensor by Using Terbium-1,10-phenanthroline-silver Nanoparticles. ANAL SCI. 2020;36(11):1345 [Crossref]
22- Sierra-Campos E, Valdez-Solana M, Avitia-Domínguez C, Campos-Almazán M, Flores-Molina I, García-Arenas G, Téllez-Valencia A. Effects of Moringa oleifera Leaf Extract on Diabetes-Induced Alterations in Paraoxonase 1 and Catalase in Rats Analyzed through Progress Kinetic and Blind Docking. Antioxidants. 2020;9(9):840 [Crossref]
23- Jena A, Rath S, Subudhi U, Dandapat J. Molecular interaction of benzo-a-pyrene inhibits the catalytic activity of catalase: Insights from biophysical and computational studies. Journal of Molecular Structure. 2022;1265:133494 [Crossref]
24- Shahraki S, Saeidifar M, Delarami H, Kazemzadeh H. Molecular docking and inhibitory effects of a novel cytotoxic agent with bovine liver catalase. Journal of Molecular Structure. 2020;1205:127590 [Crossref]
25- Shaghaghi M, Rashtbari S, Vejdani S, Dehghan G, Jouyban A, Yekta R. Exploring the interactions of a Tb(III)–quercetin complex with serum albumins (HSA and BSA): spectroscopic and molecular docking studies. Luminescence. 2020;35(4):512 [Crossref]
26- Gholami A, Dehghan G, Rashtbari S, Jouyban A. Probing the Interactions of Lamotrigine and Phenobarbital with Tau Protein: Experimental and Molecular Modeling Studies. Iran J Pharm Res. 2022;21(1) [Crossref]
27- Gholami A, Dehghan G, Rashtbari S, Jouyban A. Exploring the interaction of clonazepam and diazepam with tau protein: Multispectral and molecular docking studies. Journal of Molecular Structure. 2022;1258:132669 [Crossref]
28- Gligorijević N, Minić S, Radibratović M, Papadimitriou V, Nedić O, Sotiroudis T, Nikolić M. Nutraceutical phycocyanobilin binding to catalase protects the pigment from oxidation without affecting catalytic activity. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2021;251:119483 [Crossref]
29- Rashtbari S, Khataee S, Iranshahi M, Moosavi-Movahedi A, Hosseinzadeh G, Dehghan G. Experimental investigation and molecular dynamics simulation of the binding of ellagic acid to bovine liver catalase: Activation study and interaction mechanism. International Journal of Biological Macromolecules. 2020;143:850 [Crossref]
30- Hayat A, Alrowaili Z, Taha T, Khan J, Uddin I, Ali T, Raziq F, Ullah I, Hayat A, Palamanit A, Irfan A, Khan W. Organic heterostructure modified carbon nitride as apprehension for Quercetin Biosensor. Synthetic Metals. 2021;278:116813 [Crossref]

As a peer-reviewed international open-access journal, BioImpacts publishes articles on basic and translational aspects of pharmaceutical and biomedical sciences. 
Acceptance rate: 24% 
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