Log in

The Effect of Trifluoroethanol on Tyrosinase Activity and Conformation: Inhibition Kinetics and Computational Simulations

  • Published:
Applied Biochemistry and Biotechnology Aims and scope Submit manuscript

Abstract

We studied the inhibitory effects of trifluoroethanol (TFE) on the activity and conformation of tyrosinase. TFE increased the degree of secondary structure of tyrosinase, which directly resulted in enzyme inactivation. A reciprocal study showed that TFE inhibited tyrosinase in a slope-parabolic mixed-type inhibition manner (K I = 0.5 ± 0.096 M). Time-interval kinetic studies showed that the inhibition was best described as first order with biphasic processes. Intrinsic and 1-anilinonaphthalene-8-sulfonate-binding fluorescences were also measured to gain more insight into the supposed structural changes; these showed that TFE induced a conspicuous tertiary structural change in tyrosinase by exposing hydrophobic surfaces. We also predicted the tertiary structure of tyrosinase and simulated its docking with TFE. The docking simulation was successful with significant scores (binding energy for Autodock4 = −4.75 kcal/mol; for Dock6 = −23.07 kcal/mol) and suggested that the TRP173 residue was mainly responsible for the interaction with TFE. Our results provide insight into the structure of tyrosinase and allow us to describe a new inhibition strategy that works by inducing conformational changes rather than targeting the active site of the protein.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (Germany)

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

Abbreviations

DOPA:

3,4-Dihydroxyphenylalanine

TFE:

2,2,2-Trifluoroethanol

ANS:

1-Anilinonaphthalene-8-sulfonate

CD:

Circular dichroism

References

  1. Huang, K., Park, Y. D., Cao, Z. F., & Zhou, H. M. (2001). Biochimica et Biophysica Acta, 1545, 305–313.

    CAS  Google Scholar 

  2. Zhang, Y. X., Zhu, Y., & Zhou, H. M. (2000). The International Journal of Biochemistry & Cell Biology, 32, 887–894. doi:10.1016/S1357-2725(00)00025-X.

    Article  CAS  Google Scholar 

  3. Buck, M. (1998). Quarterly Reviews of Biophysics, 31, 297–355. doi:10.1017/S003358359800345X.

    Article  CAS  Google Scholar 

  4. Deshusses, J. M., Burgess, J. A., Scherl, A., Wenger, Y., Walter, N., Converset, V., et al. (2003). Proteomics, 3, 1418–1424. doi:10.1002/pmic.200300492.

    Article  CAS  Google Scholar 

  5. Wilkins, A. L., Yang, W., & Yang, J. J. (2003). Current Protein & Peptide Science, 4, 367–373. doi:10.2174/1389203033487063.

    Article  CAS  Google Scholar 

  6. Buck, M., Radford, S. E., & Dobson, C. M. (1993). Biochemistry, 32, 669–678. doi:10.1021/bi00053a036.

    Article  CAS  Google Scholar 

  7. Shiraki, K., Nishikawa, K., & Goto, Y. (1995). Journal of Molecular Biology, 245, 180–194. doi:10.1006/jmbi.1994.0015.

    Article  CAS  Google Scholar 

  8. Yiu, C. P., Mateu, M. G., & Fersht, A. R. (2000). ChemBioChem, 1, 49–55. doi:10.1002/1439-7633(20000703)1:1<49::AID-CBIC49>3.0.CO;2-A.

    Article  CAS  Google Scholar 

  9. Polverino de Laureto, P., Donadi, M., Scaramella, E., Frare, E., & Fontana, A. (2001). Biochimica et Biophysica Acta, 1548, 29–37.

    CAS  Google Scholar 

  10. Dubey, V. K., Shah, A., Jagannadham, M. V., & Kayastha, A. M. (2006). Protein and Peptide Letters, 13, 545–547. doi:10.2174/092986606777145823.

    Article  CAS  Google Scholar 

  11. Hamada, D., Chiti, F., Guijarro, J. I., Kataoka, M., Taddei, N., & Dobson, C. M. (2000). Nature Structural Biology, 7, 58–61. doi:10.1038/71259.

    Article  CAS  Google Scholar 

  12. Rezaei-Ghaleh, N., Ebrahim-Habibi, A., Moosavi-Movahedi, A. A., & Nemat-Gorgani, M. (2007). International Journal of Biological Macromolecules, 41, 597–604. doi:10.1016/j.ijbiomac.2007.07.018.

    Article  CAS  Google Scholar 

  13. Rezaei-Ghaleh, N., Ebrahim-Habibi, A., Moosavi-Movahedi, A. A., & Nemat-Gorgani, M. (2007). Archives of Biochemistry and Biophysics, 457, 160–169. doi:10.1016/j.abb.2006.10.031.

    Article  CAS  Google Scholar 

  14. Roccatano, D., Colombo, G., Fioroni, M., & Mark, A. E. (2002). Proceedings of the National Academy of Sciences of the United States of America, 99, 12179–12184. doi:10.1073/pnas.182199699.

    Article  CAS  Google Scholar 

  15. Invernizzi, G., & Grandori, R. (2007). Rapid Communications in Mass Spectrometry, 21, 1049–1052. doi:10.1002/rcm.2940.

    Article  CAS  Google Scholar 

  16. Soldi, G., Bemporad, F., Torrassa, S., Relini, A., Ramazzotti, M., Taddei, N., et al. (2005). Biophysical Journal, 89, 4234–4244. doi:10.1529/biophysj.105.067538.

    Article  CAS  Google Scholar 

  17. Decker, H., & Tuczek, F. (2000). Trends in Biochemical Sciences, 25, 392–397. doi:10.1016/S0968-0004(00)01602-9.

    Article  CAS  Google Scholar 

  18. Fenoll, L. G., Peñalver, M. J., Rodríguez-López, J. N., Varón, R., García-Cánovas, F., & Tudela, J. (2004). The International Journal of Biochemistry & Cell Biology, 36, 235–246. doi:10.1016/S1357-2725(03)00234-6.

    Article  CAS  Google Scholar 

  19. Ray, K., Chaki, M., & Senqupta, M. (2007). Progress in Retinal and Eye Research, 26, 323–358. doi:10.1016/j.preteyeres.2007.01.001.

    Article  CAS  Google Scholar 

  20. Gandía-Herrero, F., Jiménez, M., Cabanes, J., García-Carmona, F., & Escribano, J. (2003). Journal of Agricultural and Food Chemistry, 51, 7764–7769. doi:10.1021/jf030131u.

    Article  CAS  Google Scholar 

  21. Guerrero, A., & Rosell, G. (2005). Current Medicinal Chemistry, 12, 461–469.

    CAS  Google Scholar 

  22. Park, Y. D., Kim, S. Y., Lyou, Y. J., Lee, J. Y., & Yang, J. M. (2005). Biochimie, 87, 931–937. doi:10.1016/j.biochi.2005.06.006.

    Article  CAS  Google Scholar 

  23. Park, Y. D., Ou, W. B., Yu, T. W., & Zhou, H. M. (2001). Biochemistry and Cell Biology, 79, 479–487. doi:10.1139/bcb-79-4-479.

    Article  CAS  Google Scholar 

  24. Zhao, T. J., Ou, W. B., **e, Q., Liu, Y., Yan, Y. B., & Zhou, H. M. (2005). The Journal of Biological Chemistry, 280, 13470–13476. doi:10.1074/jbc.M413882200.

    Article  CAS  Google Scholar 

  25. Han, H. Y., Zou, H. C., Jeon, J. Y., Wang, Y. J., Xu, W. A., Yang, J. M., et al. (2007). Biochimica et Biophysica Acta, 1774, 822–827.

    CAS  Google Scholar 

  26. Park, Y. D., Lee, S. J., Park, K. H., Kim, S. Y., Hahn, M. J., & Yang, J. M. (2003). Journal of Protein Chemistry, 22, 613–623. doi:10.1023/B:JOPC.0000008726.99095.48.

    Article  CAS  Google Scholar 

  27. John, B., & Sali, A. (2003). Nucleic Acids Research, 31, 3982–3992. doi:10.1093/nar/gkg460.

    Article  CAS  Google Scholar 

  28. Rodriguez, R., Chinea, G., Lopez, N., Pons, T., & Vriend, G. (1998). Bioinformatics (Oxford, England), 14, 523–528. doi:10.1093/bioinformatics/14.6.523.

    Article  CAS  Google Scholar 

  29. Huey, R., Morris, G. M., Olson, A. J., & Goodsell, D. S. (2007). Journal of Computational Chemistry, 28, 1145–1152. doi:10.1002/jcc.20634.

    Article  CAS  Google Scholar 

  30. Moustakas, D. T., Lang, P. T., Pegg, S., Pettersen, E., Kuntz, I. D., Brooijmans, N., et al. (2006). Journal of Computer-Aided Molecular Design, 20, 601–619. doi:10.1007/s10822-006-9060-4.

    Article  CAS  Google Scholar 

  31. **e, X. Q., & Chen, J. Z. J. (2008). Chem Inf Model, 48, 465–475. doi:10.1021/ci700193u.

    Article  CAS  Google Scholar 

  32. Wei, X., Ding, S., Jiang, Y., Zeng, X. G., & Zhou, H. M. (2006). Biochemistry. Biokhimiia, 71, S77–S82. doi:10.1134/S000629790613013X.

    CAS  Google Scholar 

  33. Han, H. Y., Lee, J. R., Xu, W. A., Hahn, M. J., Yang, J. M., & Park, Y. D. (2007). Journal of Biomolecular Structure & Dynamics, 25, 165–171.

    CAS  Google Scholar 

  34. Park, Y. D., Lyou, Y. J., Hahn, H. S., Hahn, M. J., & Yang, J. M. (2006). Journal of Biomolecular Structure & Dynamics, 24, 131–138.

    CAS  Google Scholar 

  35. Park, K. H., Park, Y. D., Lee, J. R., Hahn, H. S., Lee, S. J., Bae, C. D., et al. (2005). Biochimica et Biophysica Acta, 1726, 115–120.

    CAS  Google Scholar 

  36. Park, Y. D., Jung, J. Y., Kim, D. W., Kim, W. S., Hahn, M. J., & Yang, J. M. (2003). Journal of Protein Chemistry, 22, 463–471. doi:10.1023/B:JOPC.0000005462.05642.89.

    Article  CAS  Google Scholar 

  37. Tams, J. W., & Welinder, K. G. (1996). Biochemistry, 35, 7573–7579. doi:10.1021/bi953067l.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This study was supported by a grant from the National Basic Research Program of China (no. 2006CB504100). Dr. Yong-Doo Park was supported by fund from the Science and Technology Planning Project of Jiaxing (no. 2008AZ1024), Zhejiang. Dr. Jun-Mo Yang was supported by the grants of the Korea Health 21 R&D Project (Ministry of Health, Welfare and Family Affairs, Republic of Korea, 01-PJ3-PG6-01GN12-0001 and A030003).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Hong-Wei Zhou or Fei Zou.

About this article

Cite this article

Lü, ZR., Shi, L., Wang, J. et al. The Effect of Trifluoroethanol on Tyrosinase Activity and Conformation: Inhibition Kinetics and Computational Simulations. Appl Biochem Biotechnol 160, 1896–1908 (2010). https://doi.org/10.1007/s12010-009-8730-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12010-009-8730-9

Keywords

Navigation