Skip to main content
Log in

Screening the molecular surface of human anticoagulant protein C: A search for interaction sites

  • Published:
Journal of Computer-Aided Molecular Design Aims and scope Submit manuscript

Abstract

Protein C (PC), a 62 kDa multi-modular zymogen, is activated to an anticoagulant serine protease (activated PC or APC) by thrombin bound to thrombomodulin on the surface of endothelial cells. PC/APC interacts with many proteins and the characterisation of these interactions is not trivial. However, molecular modelling methods help to study these complex biological processes and provide basis for rational experimental design and interpretation of the results. PC/APC consists of a Gla domain followed by two EGF modules and a serine protease domain. In this report, we present two structural models for full-length APC and two equivalent models for full-length PC, based on the X-ray structures of Gla-domainless APC and of known serine protease zymogens. The overall elongated shape of the models is further cross-validated using size exclusion chromatography which allows evaluation of the Stokes radius (rs for PC = 33.15 Å rs for APC = 34.19 Å), frictional ratio and axial ratio. We then propose potential binding sites at the surface of PC/APC using surface hydrophobicity as a determinant of the preferred sites of intermolecular recognition. Most of the predicted binding sites are consistent with previously reported experimental data, while some clusters highlight new regions that should be involved in protein-protein interactions.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Esmon, C.T., Gu, J.M., Xu, J., Qu, D., Stearns-Kurosawa, D.J. and Kurosawa, S., Haematologica, 84 (1999) 363.

    Google Scholar 

  2. Dahlbäck, B., Semin. Hematol., 34 (1997) 217.

    Google Scholar 

  3. Nesheim, M., Wang, W., Boffa, M., Nagashima, M., Morser, J. and Bajzar, L., Thromb. Haemost., 78 (1997) 386.

    Google Scholar 

  4. Kalafatis, M., Egan, J.O., van't Veer, C., Cawthern, K.M. and Mann, K.G., Crit. Rev. Eukaryot. Gene Expr., 7 (1997) 241.

    Google Scholar 

  5. Shen, L. and Dahlbäck, B., J. Biol. Chem., 269 (1994) 18735.

    Google Scholar 

  6. Thorelli, E., Kaufman, R.J. and Dahlbäck, B., Blood, 93 (1999) 2552.

    Google Scholar 

  7. Foster, D.C., Sprecher, C.A., Holly, R.D., Gambee, J.E., Walker, K.M. and Kumar, A.A., Biochemistry, 29 (1990) 347.

    Google Scholar 

  8. Esmon, C.T., J. Biol. Chem., 264 (1989) 4743.

    Google Scholar 

  9. Di Cera, E., Dang, Q.D. and Ayala, Y.M., Cell. Mol. Life Sci., 53 (1997) 701.

    Google Scholar 

  10. Knobe, K.E., Bernsdotter, A., Shen, L., Morser, J., Dahlbäck, B. and Villoutreix, B.O., Proteins, 35 (1999) 218.

    Google Scholar 

  11. Mather, T., Oganessyan, V., Hof, P., Huber, R., Foundling, S., Esmon, C. and Bode, W., EMBO J., 15 (1996) 6822.

    Google Scholar 

  12. Villoutreix, B.O., Teleman, O. and Dahlbäck, B., J. Comput.-Aided Mol. Design, 11 (1997) 293.

    Google Scholar 

  13. Banner, D.W., D'Arcy, A., Chene, C., Winkler, F.K., Guha, A., Konigsberg, W.H., Nemerson, Y. and Kirchhofer, D., Nature, 380 (1996) 41.

    Google Scholar 

  14. Brandstetter, H., Bauer, M., Huber, R., Lollar, P. and Bode, W., Proc. Natl. Acad. Sci. USA, 92 (1995) 9796.

    Google Scholar 

  15. McCallum, C.D., Hapak, R.C., Neuenschwander, P.F., Morrissey, J.H. and Johnson, A.E., J. Biol. Chem., 271 (1996) 28168.

    Google Scholar 

  16. Yegneswaran, S., Wood, G.M., Esmon, C.T. and Johnson, A.E., J. Biol. Chem., 272 (1997) 25013.

    Google Scholar 

  17. Mutucumarana, V.P., Duffy, E.J., Lollar, P. and Johnson, A.E., J. Biol. Chem., 267 (1992) 17012.

    Google Scholar 

  18. Ashton, A.W., Boehm, M.K., Johnson, D.J., Kemball-Cook, G. and Perkins, S.J., Biochemistry, 37 (1998) 8208.

    Google Scholar 

  19. Young, L., Jernigan, R.L. and Covell, D.G., Protein Sci., 3 (1994) 717.

    Google Scholar 

  20. Jones, S. and Thornton, J.M., Proc. Natl. Acad. Sci. USA, 93 (1996) 13.

    Google Scholar 

  21. Lum, K., Chandler, D. and Weeks, J.D., J. Phys. Chem. B, 103 (1999) 4570.

    Google Scholar 

  22. Zhang, C., Chen, J. and DeLisi, C., Proteins, 34 (1999) 255.

    Google Scholar 

  23. Tsai, C.-J. and Nussinov, R., Protein Sci., 6 (1997) 1426.

    Google Scholar 

  24. Tsai, C.-J., Lin, S.L., Wolfson, H.J. and Nussinov, R., Protein Sci., 6 (1997) 53.

    Google Scholar 

  25. Jones, S., Marin, A. and Thornton, J.M., Protein Eng., 13 (2000) 77.

    Google Scholar 

  26. Janin, J., Proteins, 28 (1997) 153.

    Google Scholar 

  27. Dasgupta, S., Iyer, G.H., Bryant, S.H., Lawrence, C.E. and Bell, J.A., Proteins, 28 (1997) 494.

    Google Scholar 

  28. Villoutreix, B.O., Härdig, Y., Wallqvist, A., Covell, D.G., García de Frutos, P. and Dahlbäck, B., Proteins, 31 (1998) 391.

    Google Scholar 

  29. Blom, A.M., Covell, D.G., Wallqvist, A., Dahlbäck, B. and Villoutreix, B.O., Biochim. Biophys. Acta, 1388 (1998) 181.

    Google Scholar 

  30. Caffrey, M., Cai, M., Kaufman, J., Stahl, S.J., Wingfield, P.T., Covell, D.G., Gronenborn, A.M. and Clore, G.M., EMBO J., 17 (1998) 4572.

    Google Scholar 

  31. Wang, D., Bode, W. and Huber, R., J. Mol. Biol., 185 (1985) 595.

    Google Scholar 

  32. Vijayalakshmi, J., Padmanabhan, K.P., Mann, K.G. and Tulinsky, A., Protein Sci., 3 (1994) 2254.

    Google Scholar 

  33. Mathews, II, Padmanabhan, K.P., Tulinksy, A. and Sadler, J.E., Biochemistry, 33 (1994) 13547.

    Google Scholar 

  34. Fuentes-Prior, P., Iwanaga, Y., Huber, R., Pagila, R., Rumennik, G., Seto, M., Morser, J., Light, D.R. and Bode, W., Nature, 404 (2000) 518.

    Google Scholar 

  35. Soriano-Garcia, M., Padmanabhan, K., de Vos, A.M. and Tulinsky, A., Biochemistry, 31 (1992) 2554.

    Google Scholar 

  36. Bernstein, F.C., Koetzle, T.F., Williams, G.J.B., Meyer, E.F. Jr., Brice, M.D., Rodgers, J.R., Kennard, O., Shimanouchi, T. and Tasmui, M., J. Mol. Biol., 112 (1977) 535.

    Google Scholar 

  37. Villoutreix, B.O., Åkerström, B. and Lindqvist, A., Blood Coag. Fibrinol., 11 (2000) 261.

    Google Scholar 

  38. Ponder, J.W. and Richards, F.M., J. Mol. Biol., 193 (1987) 775.

    Google Scholar 

  39. Shen, L., Villoutreix, B.O. and Dahlbäck, B., Thromb. Haemost., 82 (1999) 1078.

    Google Scholar 

  40. Blom, A.M., Mörgelin, M., Öyen, M., Jarvet, J. and Fries, E., J. Biol. Chem., 274 (1999) 298.

    Google Scholar 

  41. Velten, M., Villoutreix, B.O. and Ladjimi, M.M., Biochemistry, 39 (2000) 307.

    Google Scholar 

  42. Siegel, L.M. and Monty, K.J., Biochim. Biophys. Acta, 112, (1966) 346.

    Google Scholar 

  43. Deacon, M.P., Davis, S.S., Waite, J.H. and Harding, S.E., Biochemistry, 37 (1998) 14108.

    Google Scholar 

  44. Miyazawa, S. and Jernigan, R.L., Macromolecules, 18 (1985) 534.

    Google Scholar 

  45. Waxman, E., Laws, W.R., Laue, T.M., Nemerson, Y. and Alexander Ross, J.B., Biochemistry, 32 (1993) 3005.

    Google Scholar 

  46. Zhang, L. and Castellino, F.J., J. Biol. Chem., 269 (1994) 3590.

    Google Scholar 

  47. Sunnerhagen, M., Forsen, S., Hoffren, A.M., Drakenberg, T., Teleman, O. and Stenflo, J., Nat. Struct. Biol., 2 (1995) 504.

    Google Scholar 

  48. Kemball-Cook, G., Johnson, D.J.D., Tuddenham, E.G.D. and Harlos, K., J. Struct. Biol., 127 (1999) 213.

    Google Scholar 

  49. Villoutreix, B.O. and Dahlbäck, B., Protein Sci., 7 (1998) 1317.

    Google Scholar 

  50. Pemberton, S., Lindley, P., Zaitsev, V., Card, G., Tuddenham, E.G. and Kemball-Cook, G., Blood, 89 (1997) 2413.

    Google Scholar 

  51. Fisher, C.L., Greengard, J.S. and Griffin, J.H., Protein Sci., 3 (1994) 588.

    Google Scholar 

  52. Lüthy, R., Bowie, J.U. and Eisenberg, D., Nature, 356 (1992) 83.

    Google Scholar 

  53. Gerlitz, B. and Grinnell, B.W., J. Biol. Chem., 271 (1996) 22285.

    Google Scholar 

  54. Freyssinet, J.M., Gauchy, J. and Cazenave, J.P., Biochem. J., 238 (1986) 151.

    Google Scholar 

  55. Horie, S., Ishii, H., Hara, H. and Kazama, M., Biochem. J., 301 (1994) 683.

    Google Scholar 

  56. Villoutreix, B.O., Blom, A.M. and Dahlbäck, B., Protein Eng., 12 (1999) 833.

    Google Scholar 

  57. Conte, L.L., Chothia, C. and Janin, J., J. Mol. Biol., 285 (1999) 2177.

    Google Scholar 

  58. Sadler, J.E., Thromb. Haemost., 78 (1997) 392.

    Google Scholar 

  59. Öhlin, A.K., Bjork, I. and Stenflo, J., Biochemistry, 29 (1990) 644.

    Google Scholar 

  60. Mesters, R.M., Heeb, M.J. and Griffin, J.H., Biochemistry, 32 (1993) 12656.

    Google Scholar 

  61. Mesters, R.M., Heeb, M.J. and Griffin, J.H., Protein Sci., 2 (1993) 1482.

    Google Scholar 

  62. Shen, L., Villoutreix, B.O. and Dahlbäck, B., Thromb. Haemost., 82 (1999) 72.

    Google Scholar 

  63. Shen, L., Dahlbäck, B. and Villoutreix, B.O., Biochemistry, 39 (2000) 2853.

    Google Scholar 

  64. Rezaie, A.R. and Esmon, C.T., J. Biol. Chem., 25 (1993) 19943.

    Google Scholar 

  65. Heller, H., Schaefer, M. and Schulten, K., J. Phys. Chem., 97 (1993) 8360.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Villoutreix, B.O., Covell, D.G., Blom, A.M. et al. Screening the molecular surface of human anticoagulant protein C: A search for interaction sites. J Comput Aided Mol Des 15, 13–27 (2001). https://doi.org/10.1023/A:1011158717139

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1011158717139

Navigation