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Structural models of antibody variable fragments: A method for investigating binding mechanisms

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Abstract

The value of comparative molecular modeling for elucidating structure-function relationships was demonstrated by analyzing six anti-nucleosome autoantibody variable fragments. Structural models were built using the automated procedure developed in the COMPOSER software, subsequently minimized with the AMBER force field, and validated according to several standard geometric and chemical criteria. Canonical class assignment from Chothia and Lesk's [Chottin and Lesk, J. Mol. Biol., 196 (1987) 901; Chothia et al., Nature, 342 (1989) 877] work was used as a supplementary validation tool for five of the six hypervariable loops. The analysis, based on the hypothesis that antigen binding could occur through electrostatic interactions, reveals a diversity of possible binding mechanisms of anti-nucleosome or anti-histone antibodies to their cognate antigen. These results lead us to postulate that anti-nucleosome autoantibodies could have different origins. Since both anti-DNA and anti-nculeosome autoantibodies are produced during the course of systemic lupus erythematosus, a non-organ specific autoimmune disease, a comparative structural and electrostatic analysis of the two populations of autoantibodies may constitute a way to elucidate their origin and the role of the antigen in tolerance breakdown. The present study illustrates some interests, advantages and limits of a methodology based on the use of comparative modeling and analysis of molecular surface properties.

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References

  1. Bryson, J.W., Betz, S.F., Lu, H.S., Suich, D.J., Zhou, H.X., O'Neil, K.T. and DeGrado, W.F., Science, 270 (1995) 935.

    Google Scholar 

  2. Janin, J., Proteins, 21 (1995) 30.

    Google Scholar 

  3. Janin, J., Biochimie, 77 (1995) 497.

    Google Scholar 

  4. McPherson, A., The Preparation and Analysis of Protein Crystal, Wiley, New York, NY, 1982.

    Google Scholar 

  5. Zhao, D. and Jardetzky, O., J. Mol. Biol., 239 (1994) 601.

    Google Scholar 

  6. Overington, J.P., Curr. Opin. Struct. Biol., 2 (1992) 394.

    Google Scholar 

  7. Böhm, G., Biophys. Chem., 59 (1996) 1.

    Google Scholar 

  8. Sanchez, R. and Sali, A., Curr. Opin. Struct. Biol., 7 (1997) 206.

    Google Scholar 

  9. Hilbert, M., Böhm, G. and Jaenicke, R., Proteins, 17 (1993) 138.

    Google Scholar 

  10. Bruccoleri, R.E., Mol. Simul., 10 (1993) 151.

    Google Scholar 

  11. Tenette, C., Ducancel, F. and Smith, J.C., Proteins, 26 (1996) 9.

    Google Scholar 

  12. Martin, A.C.R., Cheetham, J.C. and Rees, A.R., Proc. Natl. Acad. Sci. USA, 86 (1989) 9268.

    Google Scholar 

  13. Alzari, P.M., Lascombe, M.B. and Poljak, R.J., Annu. Rev. Immunol., 6 (1988) 555.

    Google Scholar 

  14. Viswanathan, M., Anchin, J.M., Droupadi, P.R., Mandal, C., Linthicum, D.S. and Subramaniam, S., Biophys. J., 69 (1995) 741.

    Google Scholar 

  15. Tramontano, A. and Lesk, A.M., Proteins, 13 (1992) 231.

    Google Scholar 

  16. Wilson, I.A. and Stanfield, R.L., Curr. Opin. Struct. Biol., 3 (1993) 113.

    Google Scholar 

  17. Mian, I.S., Bradwell, A.R. and Olson, A.J., J. Mol. Biol., 217 (1991) 133.

    Google Scholar 

  18. Kabat, E.A., Wu, T.T., Perry, H.M., Gottesman, K.S. and Foeller, C., Sequences of Proteins of Immunological Interest, U.S. Government Printing Office, National Institutes of Health, Bethesda, MD, 1991.

    Google Scholar 

  19. Chothia, C. and Lesk, A.M., J. Mol. Biol., 196 (1987) 901.

    Google Scholar 

  20. Chothia, C., Lesk, A.M., Tramontano, A., Levitt, M., Smith-Gill, S.J., Air, G., Sheriff, S., Padlan, E.A., Davies, D., Tulip, W.R., Colman, P.M., Spinelli, S., Alzari, P.M. and Poljak, R.J., Nature, 342 (1989) 877.

    Google Scholar 

  21. Kotzin, B.L., Cell, 85 (1996) 303.

    Google Scholar 

  22. Arents, G., Burlingame, R.W., Wang, B., Love, W.E. and Moudrianakis, E.N., Proc. Natl. Acad. Sci. USA, 88 (1991) 10148.

    Google Scholar 

  23. Monestier, M. and Kotzin, B.L., Rheum. Dis. Clin. North Am., 18 (1992) 415.

    Google Scholar 

  24. Theofilopoulos, A.N. and Dixon, F.J., Adv. Immunol., 37 (1985) 269.

    Google Scholar 

  25. Brard, F., Jovelin, F., Petit, S., Tron, F. and Gilbert, D., Eur. J. Immunol., 26 (1996) 1587.

    Google Scholar 

  26. Eilat, D. and Anderson, W.F., Mol. Immunol., 31 (1994) 1377.

    Google Scholar 

  27. Radic, M.Z. and Weigert, M., Annu. Rev. Immunol., 12 (1994) 487.

    Google Scholar 

  28. Dougherty, D.A., Science, 271 (1996) 163.

    Google Scholar 

  29. Portanova, J.P., Creadon, G., Zhang, X., Smith, D.S., Kotzin, B.L. and Wysocki, L.J., Mol. Immunol., 32 (1995) 117.

    Google Scholar 

  30. Losman, M.J., Fasy, T.M., Novick, K.E. and Monestier, M., Int. Immunol., 5 (1993) 513.

    Google Scholar 

  31. Vasquez, M., Némethy, G. and Scheraga, H.A., Chem. Rev., 94 (1994) 2183.

    Google Scholar 

  32. Sali, A., Overington, J., Johnson, M.S. and Blundell, T.L., Trends Biol. Sci., 15 (1990) 235.

    Google Scholar 

  33. Srinivasan, N. and Blundell, T.L., Protein Eng., 6 (1993) 501.

    Google Scholar 

  34. SYBYL, Molecular Modeling Software v. 6.2, Theory Manual, Tripos Associates, St. Louis, MO, 1995.

  35. Sali, A. and Blundell, T.L., J. Mol. Biol., 212(1990) 403.

    Google Scholar 

  36. Overington, J., Johnson, M.S., Sali, A. and Blundell, T.L., Proc. R. Soc. London, B241 (1990) 132.

    Google Scholar 

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

    Google Scholar 

  38. Needleman, S. and Wunsch, C., J. Mol. Biol., 48 (1970) 443.

    Google Scholar 

  39. Gonnet, G.H., Cohen, M.A. and Benner, S.A., Science, 256 (1992) 1443.

    Google Scholar 

  40. Powell, M.J.D., Math. Program., 12 (1977) 241.

    Google Scholar 

  41. Weiner, S.J., Kollman, P.A., Case, D.A., Singh, U.C., Ghio, C., Alagona, G., Profeta, S. and Weiner, P.K., J. Am. Chem. Soc., 106 (1984) 765.

    Google Scholar 

  42. Weiner, S.J., Kollman, P.A., Nguyen, D.T. and Case, D.A., J. Comput. Chem., 7 (1986) 230.

    Google Scholar 

  43. Singh, U.C. and Kollman, P.A., J. Comput. Chem., 5 (1984) 129.

    Google Scholar 

  44. Laskowski, R.A., MacArthur, M.W., Moss, D.S. and Thornton, J.M., J. Appl. Crystallogr., 26 (1993) 283.

    Google Scholar 

  45. Martin, A.C.R., Proteins, 25 (1996) 130.

    Google Scholar 

  46. Heiden, W., Goetze, T. and Brickmann, J., J. Comput. Chem., 14 (1993) 246.

    Google Scholar 

  47. Connolly, M.L., J. Appl. Crystallogr., 16 (1983) 548 (QCPE Program No. 429, ‘Molecular Surface Program’).

    Google Scholar 

  48. Sander, C. and Schneider, R., Proteins, 9 (1991) 56.

    Google Scholar 

  49. Padlan, E.A., Mol. Immunol., 31 (1994) 169.

    Google Scholar 

  50. Wu, T.T., Johnson, G. and Kabat, E.A., Proteins, 16 (1993) 1.

    Google Scholar 

  51. Johnson, M.S., Srinivasan, N., Sowdhamini, R. and Blundell, T.L., Crit. Rev. Biochem. Mol. Biol., 29 (1994) 1.

    Google Scholar 

  52. Brard, F., Gilbert, D., Jovelin, F. and Tron, F., J. Autoimmun. (1997) in press.

  53. Gilbert, D., Brard, F., Margaritte, C., Delpech, A. and Tron, F., Mol. Immunol., 32 (1995) 477.

    Google Scholar 

  54. Herron, J.N., He, X.M., Ballard, D.W., Blier, P.R., Pace, P.E., Bothwell, A.L.M., Voss Jr., E.W. and Edmundson, A.B., Proteins, 11 (1991) 159.

    Google Scholar 

  55. Radic, M.Z., Mackle, J., Erikson, J., Mol, C., Anderson, W.F. and Weigert, M., J. Immunol., 150 (1993) 4966.

    Google Scholar 

  56. Cygler, M., Boodhoo, A., Lee, J.S. and Anderson, W.F., J. Biol. Chem., 262 (1987) 643.

    Google Scholar 

  57. Mol, C.D., Muir, A.K.S., Lee, J.S. and Anderson, W.F., J. Biol. Chem., 269 (1994) 3605.

    Google Scholar 

  58. Mol, C.D., Muir, A.K.S., Cygler, M., Lee, J.S. and Anderson, W.F., J. Biol. Chem., 269 (1994) 3615.

    Google Scholar 

  59. Barry, M.M., Mol, C.D., Anderson, W.F. and Lee, J.S., J. Biol. Chem., 269 (1994) 3623.

    Google Scholar 

  60. Wien, M.W., Filman, D.J., Stura, E.A., Guillot, S., Delpeyroux, F., Crainic, R. and Hogle, J.M., Nat. Struct. Biol., 2 (1995) 232.

    Google Scholar 

  61. Herron, J.N., Terry, A.H., Johnston, S., He, X.M., Guddat, L.W., Voss, E.W. and Edmundson, A.B., Biophys. J., 67 (1994) 2167.

    Google Scholar 

  62. Rose, D.R., Przybylska, M., To, R.J., Kayden, C.S., Oomen, R.P., Vorberg, E., Young, N.M. and Bundle, D.R., Protein Sci., 2 (1993) 1106.

    Google Scholar 

  63. Shlomchik, M.J., Mascelli, M.A., Shan, H., Radic, M.Z., Pisetsky, D.S., Marshak-Rothstein, A. and Weigert, M., J. Exp. Med., 171 (1990) 265.

    Google Scholar 

  64. Amoura, Z., Chabre, H., Koutouzov, S., Lotton, C., Cabrespines, A., Bach, J.F. and Jacob, L., Arthritis Rheum., 37 (1994) 1684.

    Google Scholar 

  65. Burlingame, R.W., Rubin, R.L., Balderas, R.S. and Theofilopoulos, A.N., J. Clin. Invest., 91 (1993) 1687.

    Google Scholar 

  66. Chabre, H., Amoura, Z., Piette, J.C., Godeau, P., Bach, J.F. and Koutouzov, S., Arthritis Rheum., 38 (1995) 1485.

    Google Scholar 

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Petit, S., Brard, F., Coquerel, G. et al. Structural models of antibody variable fragments: A method for investigating binding mechanisms. J Comput Aided Mol Des 12, 147–163 (1998). https://doi.org/10.1023/A:1007937823079

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