Skip to main content
Log in

Exploring the molecular basis of selectivity in A1 adenosine receptors agonists: a case study

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

Abstract

Adenosine is a naturally occurring purine nucleoside that has a wide variety of well-documented regulatory functions and physiological roles. Selective activation of the adenosine A1 receptor has drawn attention in drug discovery for the therapeutic effects on neural and cardiovascular disorders. We have developed a model of the human A1 adenosine receptor using bovine rhodopsin as a template. A flexible docking approach has been subsequently carried out for evaluating the molecular interactions of twenty-one selective A1 agonists with the receptor model. The results of these studies are consistent with mutational and biochemical data. In particular, they highlight a wide hydrogen-bonding network between the nucleoside portion of the ligands and the A1 receptor as well as key amino acids for hydrophobic interactions with the different N6-groups of the agonists. The models presented here provide a detailed molecular map for the selective stimulation of the adenosine A1 receptor subtype and a steady basis for the rational design of new A1 selective ligands.

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.

Institutional subscriptions

Similar content being viewed by others

References

  1. Dunwiddie, T.V., Masino, S., Annu. Rev. Neurosci., 24 (2001) 31.

    Google Scholar 

  2. Klotz, K.N., Naunyn-Schmiedeberg's Arch. Pharmacol., 362 (2000) 382.

    Google Scholar 

  3. Hess, S., Exp. Opin. Ther. Patents, 11 (2001) 1533.

    Google Scholar 

  4. IJzerman, A.P., van Galen, P.J.M., Jacobson, K.A., Drug Des. Discov., 9 (1992) 49.

    Google Scholar 

  5. Baraldi P.G., Cacciari B., Moro S., Spalluto G., Pastorin G., Da Ros T., Klotz K.N., Varani K., Gessi S., Borea P.A., J. Med. Chem., 45 (2002) 770.

    Google Scholar 

  6. Baraldi, P.G., Cacciari, B., Romagnoli, R., Spalluto, G., Exp. Opin. Ther. Patents, 9 (1999) 515.

    Google Scholar 

  7. Palczewski, K., Kumasaka, T., Hori, T., Behnke, C.A., Motoshima, H., Fox, B.A., Le Trong, I., Teller, D.C., Okada, T., Stenkamp, R.E., Yamamoto, M., Miyano, M., Science, 289 (2000) 739.

    Google Scholar 

  8. a) Muller, C.E., Curr. Med. Chemistry, 7 (2000) 1269; b) Knutsen, L.J.S., Lau, J., Petersen, H., Thomsen, C., Weis, J.U., Shalmi, M., Judge, M.E., Hansen, A.J., Sheardown, M.J., J. Med. Chem., 42 (1999) 3463.

    Google Scholar 

  9. Bairoch, A., Apweiler, R., Nucleic Acids Res., 28 (2000) 45.

    Google Scholar 

  10. Thompson, J.D., Higgins, D.G., Gibson, T.J., Nucleic Acids Res., 22 (1994) 4673.

    Google Scholar 

  11. Morgenstern, B., Frech, K., Dress, A., Werner, T., Bioinformatics, 14 (1998) 290.

    Google Scholar 

  12. Clamp, M., http://www.ebi.ac.uk/~michele/jalview/, (1998).

  13. Jones, D.T., Taylor, W.R., Thornton, J.M., Biochemistry, 33 (1994) 3038.

    Google Scholar 

  14. Jones, D.T., J. Mol. Biol., 287 (1999)797.

    Google Scholar 

  15. a) Rost, B. and Sander, C., J. Mol. Biol., 232 (1993), 584; b) Rost, B. and Sander C., Proteins, Struct. Funct. Genet., 19 (1994) 55; c) Rost, B., Sander, C., Schneider, R., CABIOS, 10 (1994) 53.

    Google Scholar 

  16. Jones, D.T., J. Mol. Biol. 292 (1999) 195.

    Google Scholar 

  17. Berman, H.M., Westbrook, J., Feng, Z., Gilliland, G., Beth, T.N., Weissig, H., Shindyalov, I.N., Bourne, P.E., Nucleic Acids Res., 28 (2000) 235.

    Google Scholar 

  18. Šali, A., Blundell, T.L., J. Mol. Biol., 234 (1993) 779.

    Google Scholar 

  19. a) Jones, T.A., Thirup, S., EMBO J., 5 (1986) 819; b) Claessens, M., Van Cutsem, E., Lasters, I., Wodak, S., Prot. Eng., 2 (1989) 335.

    Google Scholar 

  20. Pearlman, D.A., Case, D.A., Caldwell, J.W., Kollman, P., Comp. Phys. Comm., 91 (1995) 1.

    Google Scholar 

  21. Laskowski, R.A., MacArthur, M.W., Moss, D.S., Thornton, J.M., J. Appl. Cryst., 26 (1993) 283.

    Google Scholar 

  22. McMartin C., Bohacek R., J. Comput. Aided-Mol. Des., 11 (1997) 333.

    Google Scholar 

  23. Olah, M.E., Ren, H., Ostrowski, J., Jacobson, K.A., Stiles, G., J. Biol. Chem., 267 (1992) 10764.

    Google Scholar 

  24. Townsend-Nicholson, A., Schonfeld, P.R., J. Biol. Chem., 269 (1994) 2373.

    Google Scholar 

  25. Rivkees, S.A., Barbhaiya, H., Ijzerman, A.P., J. Biol. Chem., 274 (1999) 3617.

    Google Scholar 

  26. Barbhaiya, H., McClain, R., Ijzerman, A.P., Rivkees, S.A., Mol. Pharmacol., 50 (1996) 1635.

    Google Scholar 

  27. Fredholm, B.B., Ijzerman, A.P., Jacobson, K.A., Klota, K.-N., Linden J., Pharmacol. Rev., 53 (2001) 527.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Giordanetto, F., Fossa, P., Menozzi, G. et al. Exploring the molecular basis of selectivity in A1 adenosine receptors agonists: a case study. J Comput Aided Mol Des 17, 39–51 (2003). https://doi.org/10.1023/A:1024530029922

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1024530029922

Navigation