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Tytuł artykułu

The Study of Conformational Equilibrium of c[Gln-Trp-Phe-Gly-Leu-Met], a NK-2 Tachykinin Antagonist

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Conformational studies of NK-2 tachykinin antagonist c[Gln-Trp-Phe-Gly-Leu-Met] were performed using a combination of two-dimensional NMR spectroscopy and theoretical methods. The three dimensional structure of the peptide studied was determined by global conformational search, using the EDMC method with the ECEPP/3 force field and subsequent calculation of statistical weights of the obtained conformations by fitting the theoretical NOESY spectra and vicinal coupling constants 3JNHH_ to the experimental ones. Using this approach, a set of six conformations with statistical weights higher than 3% was obtained. The first two ones with the values of statistical weights over 30% can be considered as dominant ones. The structure of the most populated conformation is stabilized by type IV _-turn around Trp7-Phe8 and a _-turn centered at Trp7. In the second one, two _ turns were found: II and III_ around Met11-Gln6 and Gln6-Trp7, respectively. In both conformations, the aromatic groups of Trp7 and Phe8 are almost perpendicularly oriented to the peptide backbone. The results obtained correlate well with those published for the peptide studied by three other groups. In contrast to the results obtained by other groups, which used interproton distances as constrains, the approach described here enables to determine the conformational equilibrium of the peptide studied.
Słowa kluczowe
Rocznik
Strony
807--814
Opis fizyczny
Bibliogr. 23 poz., rys.
Twórcy
  • Faculty of Chemistry, University of Gdańsk, Sobieskiego 18, PL-80-952 Gdańsk, Poland
  • Faculty of Chemistry, University of Gdańsk, Sobieskiego 18, PL-80-952 Gdańsk, Poland
  • v
autor
  • Faculty of Chemistry, University of Gdańsk, Sobieskiego 18, PL-80-952 Gdańsk, Poland
autor
  • Faculty of Chemistry, University of Gdańsk, Sobieskiego 18, PL-80-952 Gdańsk, Poland
Bibliografia
  • 1. Williams B.J., Curtis N.R., McKnight A.T., Maquire J., Foster A. and Tridgett R., Regul. Peptides, 22, 189(1988).
  • 2. McKnight A.T., Maquire J., Williams B.J., Foster A., Tridgett R. and Iverson R., Regul. Peptides, 22, 127(1988).
  • 3. Wollbom U., Brunne R.M., Harting J., Hölzemann G. and Leibfritz D., Int. J. Pept. Protein Res., 41,376 (1993).
  • 4. Siahaan T.J. and Lutz K., J. Pharm. Biomed. Anal., 12, 65 (1994).
  • 5. Amodeo P., Rovero P., Saviano G. and Temussi P.A., Int. J. Pept. Protein Res., 44, 556 (1994).
  • 6. Malicka J., Groth M., Czapiewski C., Kasprzykowska R., Liwo A., Łankiewicz L. and Wiczk W., LIPS, 5, 45 (1998).
  • 7. Groth M., Malicka J., Czapiewski C., Liwo A., Łankiewicz L. and Wiczk W., J. Biomol. NMR, 15, 315 (1999).
  • 8. http://www.tc.comell.edu/resource/CompBiologyTools/analyze.
  • 9. Rodziewicz-Motowidlo S., Lesner A., Łęgowska A., Czapiewski C., Liwo A. and Rolka K., J. Pept. Res., 58, 159(2001).
  • 10. Koźmiński W., J. Magn. Res., 134, 189 (1998).
  • 11. Ripoll D. R. and Scheraga H., Biopolymers, 27, 1283 (1988).
  • 12. Nemethy G., Gibson K.D., Palmer K.A., Yoon C.N., Paterlini G., Zagari A., Rumsey S. and Scheraga
  • H. A., J. Phys. Chem., 96, 6472 (1992).
  • 13. Vila J., Williams R.L., Väsquez M. and Scheraga H.A., Proteins Struct., Fund. Genet., 10,199 (1991).
  • 14. Ripoll D.R., Pottle M.S., Gibson K.D., Liwo A. and Scheraga H.A., J. Comput. Chem., 16,1153 (1995).
  • 15. Ripoll D.R., Liwo A. and Czapiewski C., TASK Quart., 3, 313 (1999).
  • 16. Späth H.J., Comput. Chem., 10, 209 (1980).
  • 17. Massefski W., Jr., and Bolton P.H., J. Magn. Reson., 65, 526 (1985).
  • 18. Meadows R.P., Post C.B., Luxon B.A. and Gorenstein D.G., MORASS 2.1, Purdue University, W. Lafayette, (1994).
  • 19. Post C.B., Meadows R.P. and Gorenstein D.G., J. Am. Chem. Soc., 112, 6796 (1990).
  • 20. Bystrov V.F., Progr. NMR Spectrosc., 10, 41 (1976).
  • 21. Lewis P.N., Momany F.A. and Scheraga H.A., BBA, 303, 211 (1973).
  • 22. Pavone V., Pedone C., Lombardi A., QuartaraL. and Maggi C.A., Peptides: Chemistry, Structure and Biology. Proceedings of 13th American Peptide Symposium (R.S Hodges and J.A. Smith, eds.), ESCOM Leiden 1994, p. 487.
  • 23. Lombardi A., D’Auria G., Saviano M., Maglio O., Nastri F., Quartara L., Pedone C. and Pavone V., Biopolymers, 40, 505 (1996).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0020-0091
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