Tamoxifen inhibits the anion channel induced by Staphylococcus aureus α-hemolysin: electrophysiological and docking analysis

Authors

DOI:

https://doi.org/10.33448/rsd-v10i2.12326

Keywords:

Tamoxifen; Staphylococcus aureus; Ion channel; Virulence factors; Anti-bacterial agent.

Abstract

To investigate the effects of tamoxifen on Staphylococcus aureus α-hemolysin channel (α-HL) in planar lipid bilayers with electrophysiological characterization and docking studies. Planar lipid bilayer membranes were prepared and α-HL (0.07 mg/mL) was added to the standard solution in cis compartment of the experimental chamber. All experiments were performed at room temperature using an Axopatch 200A amplifier in the voltage clamp mode. At pH 7.5, α-HL channels were usually in a high conductance ~4 nS and rarely switch to low conductance states. After the ion channel was incorporated in bilayer membrane, the tamoxifen was also added to the standard solution to the cis compartment. To docking studies, atomics coordinates for the α-HL heptameric channel was retrieved from PDB ID (7AHL) and the structure of tamoxifen was removed from the Pubchem, their coordinates were built and minimized with Avogadro software. The molecular docking experiments were performed using the Dockthor online portal. The tamoxifen inhibited (P < 0.05) α-HL channel conductance and it was a voltage-dependent manner. The three best docking solutions and the α-HL channel were evaluated, it was observed the connection mode with the highest affinity of interaction has a greater number of types of polar interaction. The residues present interactions of greater energy were 111 and 147 that form the remainders of the constriction in the channel of α-HL. The other conformers were accommodated in a region with more hydrophobic characteristics (valine 149). The mechanism of Staphylococcus aureus α-hemolysin inhibition by tamoxifen was blockade over the constriction of channel.

Author Biographies

Luciana Ramos Teixeira, Faculdade de Medicina de Olinda

Professor at Laboratory of Functional Practices 

Janilson José da Silva Júnior, Universidade Federal de Pernambuco

Department of Biophysics and Radiobiology

Pedro Higor Saraiva Vieira, Faculdade de Medicina de Olinda

Student of Programa de Desenvolvimento Institucional de Iniciação Científica (PRODIIC)

Marcus Vinícius Guerra Canto, Faculdade de Medicina de Olinda

Student

Anne Gabryelle Maciel de Figueirêdo, Faculdade de Medicina de Olinda

Student

Joelmir Lucena Veiga da Silva, Faculdade de Medicina de Olinda

Professor at Laboratory of Functional Practices

References

Bryant, A. E., Gomi, S., Katahira, E., Huang, D. B., & Stevens, D. L. (2019). The effects of iclaprim on exotoxin production in methicillinresistant and vancomycin-intermediate Staphylococcus aureus. Journal of Medical Microbiology, 68, 456–466. https://doi.org/10.1099/jmm.0.000929

Fussle, R., Bhakdi, S. Sziegoleit, A., Tranum-Jensen, J., Kranz, T., & Wellensiek, H. J. (1981). On the mechanism of membrane damage by Staphylococcus aureus alpha-toxin. Journal of Cell Biology, 91, 83-94. https://doi.org/10.1083/jcb.91.1.83

Gómez-Coronado, D., Lasunción, M. A., Martínez-Botas, J., & Fernández-Suárez, M. E. (2020). Role of cholesterol metabolism in the anticancer pharmacology of selective estrogen receptor modulators. Seminars in Cancer Biology, S1044-579X(20), 30187-5. https://doi.org/10.1016/j.semcancer.2020.08.015

Gouaux, J. E., Braha, O., Hobaugh, M. R., Song, L., Cheley, S., Shustak, C., & Bayley, H. (1994). Subunit stoichiometry of staphylococcal alpha-hemolysin in crystals and on membranes: a heptameric transmembrane pore. Proceedings of the National Academy of Sciences of the USA, 91, 12828–31. https://doi.org/10.1073/pnas.91.26.12828

Hanwell, M. D., Curtis, D. E., Lonie, D. C., Vandermeersch, T., Zurek, E., & Hutchison, G. R. (2012). Avogadro: An advanced semantic chemical editor, visualization, and analysis platform. Journal of Cheminformatics, 4(1), 17. https://doi.org/10.1186/1758-2946-4-17

Imberti, R., Garavaglia, M. L., Verduci, I., Cannavale, G., Balduzzi, G., Papetti, S., & Mazzanti, M. (2018). Antiestrogen- and tamoxifen-induced effects on calcium-activated chloride currents in epithelial cells carrying the ΔF508-CFTR point mutation. Respiratory Research, 19, 198. https://doi.org/10.1186/s12931-018-0901-1

Júnior, J. J. S., Soares, T. A., Pol-Fachin, L., Machado, D. C. Rusu, V. H., Aguiar, J. P., & Rodrigues, C. G. (2019). Alpha-hemolysin nanopore allows discrimination of the microcystins variants. RSC Advances, 9, 14683. https://doi.org/10.1039/c8ra10384d

Karginov, V. A., Nestorovich, E. M, Schmidtmann, F., Robinson, T. M., Yohannes, A., Fahmi, N. E., Bezrukov, S. M., & Hecht, S. M. (2007). Inhibition of S. aureus alpha-hemolysin and B. anthracis lethal toxin by beta-cyclodextrin derivatives. Bioorganic & Medicinal Chemistry, 15(16), 5424–31. https://doi.org/10.1016/j.bmc.2007.05.058

Krasilnikov, O. V., Merzlyak, P. G., Yuldasheva, L. N., Rodrigues, C. G., & Nogueira R. A. (1999). Heparin influence on alpha-staphylotoxin formed channel. Biochimica et Biophysica Acta, 1417(1), 167–82. https://doi.org/10.1016/s0005-2736(98)00244-2

Krasilnikov, O. V., Merzlyak, P. G. Sabirov, R. Z., Ternovsky, V. I., & Zaripova, R. K. (1988). Effect of pH on the potential-dependence of staphylococcal toxin channels functioning in phosphatidylcholine bilayer. Ukrainskiĭ Biokhimicheskiĭ Zhurnal, 60(6), 60–66. Retrieved from https://europepmc.org/article/med/2467413

Krasilnikov, O. V., Merzlyak, P. G., Yuldasheva, L. N., Rodrigues, C. G., Bhakdi, S., & Valeva, A. (2000). Electrophysiological evidence for heptameric stoichiometry of ion channels formed by Staphylococcus aureus alpha-toxin in planar lipid bilayers. Molecular Microbiology, 37(6), 1372–8. https://doi.org/10.1046/j.1365-2958.2000.02080.x

Liu, J., Kozhaya, L., Torres, V. J., Unutmaz, D., & Lu, M. (2020). Structure-based discovery of a small-molecule inhibitor of methicillin-resistant Staphylococcus aureus virulence. Journal of Biological Chemistry, 295(18), 5944-5959. https://doi.org/10.1074/jbc.RA120.012697

Magalhães, C. S., Almeida, D. M., Barbosa, H. J. C., & Dardenne, L. E. (2014). A dynamic niching genetic algorithm strategy for docking of highly flexible ligands. Information Sciences, 289, 206–24. https://doi.org/10.1016/j.ins.2014.08.002

Melo, M. C. A., Teixeira, L. R., Pol-Fachin, L., & Rodrigues C. G. (2016). Inhibition of the hemolytic activity caused by Staphylococcus aureus alpha-hemolysin through isatin-Schiff copper(II) complexes. FEMS Microbiology Letters, 363(1), fnv207. https://doi.org/10.1093/femsle/fnv207

Montal, M., & Mueller, P. (1972). Formation of bimolecular membranes from lipid monolayers and a study of their electrical properties. Proceedings of the National Academy of Sciences of the USA, 69(12), 3561–6. https://doi.org/10.1073/pnas.69.12.3561

Pereira, A. S., Shitsuka, D. M., Parreira, F. J., & Shitsuka, R. (2018). Metodologia da pesquisa científica. Santa Maria, RS: UFSM, NTE. http://repositorio.ufsm.br/handle/1/15824

Ponce-Balbuena, D., López-Izquierdo, A., Ferrer, T., Rodríguez-Menchaca, A. A., Aréchiga-Figueroa, I. A., & Sánchez-Chapula, J. A. (2009). Tamoxifen inhibits inward rectifier K+ 2.x family of inward rectifier channels by interfering with phosphatidylinositol 4,5-bisphosphate-channel interactions. Journal of Pharmacology and Experimental Therapeutics, 331(2), 563-573. https://doi.org/10.1124/jpet.109.156075

Qiu, J., Wang, D., Zhang, Y., Dong, J., Wang, J., & Niu, X. (2013). Molecular modeling reveals the novel inhibition mechanism and binding mode of three natural compounds to Staphylococcal alpha-hemolysisn. Public Library of Science One, 8(11), e80197. https://doi.org/10.1371/journal.pone.0080197

Rani, N., Saravanan, V., Lakshmi, P. T. V., & Annamalai, A. (2014). Inhibition of pore formation by blocking the assembly of Staphylococcus aureus a-hemolysin through a novel peptide inhibitor: an in silco approach. International Journal of Peptide Research and Therapeutics, 20, 575–83. https://doi.org/10.1007/s10989-014-9424-x

Rodrigues, C. G, Machado, D. C., Da Silva, A. M. B., Júnior, J. J. S., & Krasilnikov, O. V. (2011). Hofmeister effect in confined spaces: halogen ions and single molecule detection. Biophysical Journal, 100(12), 2929–35. https://doi.org/10.1016/j.bpj.2011.05.003

Silva, H. R., Rocha, Álvaro S. C., Rocha, M. V. S., Veras, D. M., Sousa, O. M. C. de, Sousa, G. da C., Almeida, D. F., Oliveira, A. L. P. de, Bezerra, G. S. S., Ribeiro, D. A. dos S., Pereira, N. M., Alves, A. K. R., Alves, A. K. R., Silva, B. B. L. da, Nogueira, F. D., Rodrigues, S. L. G., & Pessoa, G. T. (2020). Reflection of environmental imbalance in health: multi-resistant bacteria in hospital environment. Research, Society and Development, 9(8), e220985604. https://doi.org/10.33448/rsd-v9i8.5604

Song, L., Hobaugh, M. R., Shustak, C., Stephen, C., Bayley, H., & Gouaux, J. E. (1996). Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore. Science, 274(5294), 1859–65. https://doi.org/10.1126/science.274.5294.1859

Teixeira, L. R., Merzlyak, P. G., Valeva, A., & Krasilnikov, O. V. (2009). Interaction of heparins and dextran sulfates with a mesoscopic protein nanopore. Biophysical Journal, 97(11), 2894–903. https://doi.org/10.1016/j.bpj.2009.09.019

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Published

09/02/2021

How to Cite

TEIXEIRA, L. R. .; SILVA JÚNIOR, J. J. da .; VIEIRA, P. H. S.; CANTO, M. V. G.; FIGUEIRÊDO, A. G. M. de .; SILVA, J. L. V. da. Tamoxifen inhibits the anion channel induced by Staphylococcus aureus α-hemolysin: electrophysiological and docking analysis. Research, Society and Development, [S. l.], v. 10, n. 2, p. e13010212326, 2021. DOI: 10.33448/rsd-v10i2.12326. Disponível em: https://rsdjournal.org/index.php/rsd/article/view/12326. Acesso em: 23 apr. 2024.

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Section

Health Sciences