Tytuł artykułu
Identyfikatory
Warianty tytułu
Języki publikacji
Abstrakty
The cyclic hexadecapeptide containing human heat shock protein 70(29-42) fragment cyclized by the disulfide bridge between two L-cysteine residues introduced at the N- and C-termini was synthesized by the solid phase method. It was established that the cyclic analogue, contrary to its linear counterpart, had much lower ability to generate immune response in rabbits. Conformational studies of cyclic peptide performed using 1D and 2D 1H-NMR spectroscopy in conjunction with theoretical conformational analysis revealed that the cyclization constrained the 3D structure of this peptide, reflected by the observed rate of cis/trans isomerization of Arg9-Thr10 peptide bond and the presence of Gly7-Asn8 peptide bond in cis geometry.We, therefore, postulate that the conformational flexibility in the case of Human Heat Shock Protein fragments is a key element for their immunogenicity.
Wydawca
Czasopismo
Rocznik
Tom
Strony
265--273
Opis fizyczny
Bibliogr. 16 poz., rys.
Twórcy
autor
- Faculty of Chemistry, University of Gdansk, 80-952 Gdansk, Poland
autor
- Faculty of Chemistry, University of Gdansk, 80-952 Gdansk, Poland
autor
- Institute of Maritime and Tropical Medicine, 80-915 Gdynia, Poland
autor
- Faculty of Chemistry, University of Gdansk, 80-952 Gdansk, Poland
autor
- Faculty of Chemistry, University of Gdansk, 80-952 Gdansk, Poland
autor
- Institute of Maritime and Tropical Medicine, 80-915 Gdynia, Poland
autor
- Faculty of Chemistry, University of Gdansk, 80-952 Gdansk, Poland
Bibliografia
- 1. Lindquist S., Ann. Rev. Biochem., 55, 1151 (1986).
- 2. Skowyra Z. and Żylicz M., Post. Bioch,, 33, 259 (1987).
- 3. Lipińska B., Post. Bioch., 36, 32 (1990).
- 4. Karawajczyk B., Wysocki J., Kunikowska D,, Mackiewicz Z., Głośnicka R., Korzeniowski A., Górski J. and Kupryszewski G., Polish J. Chem., 72, 1017 (1998).
- 5. Rizo J. and Gierasch L.M., Ann. Rev. Biochem., 61, 387 (1992).
- 6. Barany B.F. and Merrifield R.B., The Peptides Analysis, Synthesis, Biology. Vol. 2, (Eds. Gross E. and Mainenhofer J.), Acad. Press, N Y, 1980, p. 3.
- 7. Gism B.F., Helv. Chim. Acta, 56, 1476 (1973).
- 8. Kaiser E., Colescoft R,, Bossinger C.D. and Cool P.J., Anal Biochem., 34, 595 (1977).
- 9. Tam J.P., Health W.F. and Merrifield R.B., J. Am. Chem. Soc., 105, 6442 (1983).
- 10. Veber D.F., Milkowski J.D., Varga S., Denkewalter R.G. and Hirschmann R., J. Am. Chem. Soc., 94, 5456 (1972).
- 11. Kamber B., Helv, Chim. Acta, 54, 927 (1971),
- 12. Bruenger A., X-PLOR 3.2, Yale Univ. Press, New Haven (1993).
- 13. Brooks B., Bruccoleri R., Olafson B.O., States D.J., Swaminathan S. andKarplusM., J. Comp. Chem.,4, 187(1993).
- 14. Powell M.J.D., Math. Prog., 12, 241 (1977).
- 15. Lewis P.N., Momany F.A. and Scheraga H.A., Biochim. Biophys. Acta, 303, 211 (1973).
- 16. Cresswell P. and Howard J., Curr. Opin Immunol, 11, 61 (1999).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0016-0078