Literature DB >> 16078190

Beta-hairpin formation in aqueous solution and in the presence of trifluoroethanol: a (1)H and (13)C nuclear magnetic resonance conformational study of designed peptides.

Clara M Santiveri1, David Pantoja-Uceda, Manuel Rico, M Angeles Jiménez.   

Abstract

In order to check our current knowledge on the principles involved in beta-hairpin formation, we have modified the sequence of a 3:5 beta-hairpin forming peptide with two different purposes, first to increase the stability of the formed 3:5 beta-hairpin, and second to convert the 3:5 beta-hairpin into a 2:2 beta-hairpin. The conformational behavior of the designed peptides was investigated in aqueous solution and in 30% trifluoroethanol (TFE) by analysis of the following nuclear magnetic resonance (NMR) parameters: nuclear Overhauser effect (NOE) data, and C(alpha)H, (13)C(alpha), and (13)C(beta) conformational shifts. From the differences in the ability to adopt beta-hairpin structures in these peptides, we have arrived to the following conclusions: (i) beta-Hairpin population increases with the statistical propensity of residues to occupy each turn position. (ii) The loop length, and in turn, the beta-hairpin type, can be modified as a function of the type of turn favored by the loop sequence. These two conclusions reinforce previous results about the importance of beta-turn sequence in beta-hairpin folding. (iii) Side-chain packing on each face of the beta-sheet may play a major role in beta-hairpin stability; hence simplified analysis in terms of isolated pair interactions and intrinsic beta-sheet propensities is insufficient. (iv) Contributions to beta-hairpin stability of turn and strand sequences are not completely independent. (v) The burial of hydrophobic surface upon beta-hairpin formation that, in turn, depends on side-chain packing also contributes to beta-hairpin stability. (vi) As previously observed, TFE stabilizes beta-hairpin structures, but the extent of the contribution of different factors to beta-hairpin formation is sometimes different in aqueous solution and in 30% TFE. (c) 2005 Wiley Periodicals, Inc. Biopolymers 79: 150-162, 2005.

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Year:  2005        PMID: 16078190     DOI: 10.1002/bip.20345

Source DB:  PubMed          Journal:  Biopolymers        ISSN: 0006-3525            Impact factor:   2.505


  9 in total

1.  13C structuring shifts for the analysis of model β-hairpins and β-sheets in proteins: diagnostic shifts appear only at the cross-strand H-bonded residues.

Authors:  Irene Shu; Michele Scian; James M Stewart; Brandon L Kier; Niels H Andersen
Journal:  J Biomol NMR       Date:  2013-07-14       Impact factor: 2.835

2.  Environmental polarity induces conformational transitions in a helical peptide sequence from bacteriophage T4 lysozyme and its tandem duplicate: a molecular dynamics simulation study.

Authors:  Harpreet Kaur; Yellamraju U Sasidhar
Journal:  J Mol Model       Date:  2015-03-17       Impact factor: 1.810

3.  Design and NMR conformational study of a beta-sheet peptide based on Betanova and WW domains.

Authors:  Ana M Fernández-Escamilla; Salvador Ventura; Luis Serrano; M Angeles Jiménez
Journal:  Protein Sci       Date:  2006-09-08       Impact factor: 6.725

4.  β-Sheet 13C structuring shifts appear only at the H-bonded sites of hairpins.

Authors:  Irene Shu; James M Stewart; Michele Scian; Brandon L Kier; Niels H Andersen
Journal:  J Am Chem Soc       Date:  2011-01-07       Impact factor: 15.419

5.  Micelle-Triggered β-Hairpin to α-Helix Transition in a 14-Residue Peptide from a Choline-Binding Repeat of the Pneumococcal Autolysin LytA.

Authors:  Héctor Zamora-Carreras; Beatriz Maestro; Erik Strandberg; Anne S Ulrich; Jesús M Sanz; M Ángeles Jiménez
Journal:  Chemistry       Date:  2015-04-27       Impact factor: 5.236

6.  VCD spectroscopic properties of the beta-hairpin forming miniprotein CLN025 in various solvents.

Authors:  Marcus P D Hatfield; Richard F Murphy; Sándor Lovas
Journal:  Biopolymers       Date:  2010-05       Impact factor: 2.505

7.  The effect of the cosolvent trifluoroethanol on a tryptophan side chain orientation in the hydrophobic core of troponin C.

Authors:  Olivier Julien; Pascal Mercier; Melissa L Crane; Brian D Sykes
Journal:  Protein Sci       Date:  2009-06       Impact factor: 6.725

Review 8.  beta-hairpin-forming peptides; models of early stages of protein folding.

Authors:  Agnieszka Lewandowska; Stanisław Ołdziej; Adam Liwo; Harold A Scheraga
Journal:  Biophys Chem       Date:  2010-05-06       Impact factor: 2.352

9.  Assessing the Ability of Spectroscopic Methods to Determine the Difference in the Folding Propensities of Highly Similar β-Hairpins.

Authors:  Hanna Andersson; Emma Danelius; Patrik Jarvoll; Stephan Niebling; Ashley J Hughes; Sebastian Westenhoff; Ulrika Brath; Máté Erdélyi
Journal:  ACS Omega       Date:  2017-02-13
  9 in total

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