Nuclear‐magnetic‐resonance studies on the conformations of tridecapeptide α‐mating factor from yeast Saccharomyces cerevisiae and analog peptides in aqueous solution
- 1 April 1984
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 140 (1) , 163-171
- https://doi.org/10.1111/j.1432-1033.1984.tb08081.x
Abstract
The conformation of tridecapeptide .alpha.-mating factor from S. cerevisiae in aqueous solution was analyzed, in comparison with those of active analog and inactive analog peptides. 270-MHz 1H-NMR spectra of these peptides were observed and the spectral patterns of main-chain N-H proton resonances were classified into 3 groups. .alpha.-mating factor and Trp1-bearing active peptides belong to the group A1, active des-Trp1-peptides belong to the group A2 while the peptides of group B are inactive. The main-chain N-H proton resonances of the groups A1 and A2 and side-chain N-H proton resonances were all assigned to individual residues. The 13C-NMR analysis of .alpha.-mating factor indicates that the Lys7-Pro8 and Gln10-Pro11 peptide bonds exclusively take the trans form. From the temperature and pH dependence of chemical shifts and Gd(III)-induced relaxation enhancements of amide proton resonances, .alpha.-mating factor is found to take partly a folded conformation in aqueous solution, with an .alpha.-helical form in the N-terminal domain and 2 .beta.-turn forms in the central and C-terminal domain. The pH dependence of fluorescence intensity indicates that, in this folded conformation, the C-terminal carboxylate group lies close to the N-terminal domain. The presence of the folded form in the N-terminal domain and the .beta.-turn form in the central domain correlates with the biological activity of .alpha.-mating factor and analog peptides. However, the folded conformation of .alpha.-mating factor is in equilibrium with predominantly unordered form, as found from the circular dichroism and NMR analyses. The N-H proton and C-.alpha. proton resonances of free .alpha.-mating factor as assigned in the present study allow the transferred nuclear Overhauser enhancement (NOE) analysis of the membrane-bound conformation that is more directly related with the activity.This publication has 24 references indexed in Scilit:
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