Literature DB >> 8075391

Conformational study of sequential Lys and Leu based polymers and oligomers using vibrational and electronic CD spectra.

V Baumruk1, D Huo, R K Dukor, T A Keiderling, D Lelievre, A Brack.   

Abstract

Vibrational CD (VCD) and electronic CD (ECD) spectra of some sequential Lys and Leu based oligo- and polypeptides were studied as a function of added salt and (for ECD) as a function of concentration in aqueous solution. For these samples, the VCD spectra can only be measured at relatively high concentrations under which the well-known salt-induced transition to a beta-sheet form can be observed for the KL based species, but only the end-state alpha-helical conformation is obvious for the LKKL based samples. ECD concentration dependence demonstrates that, at high concentration with no added or with added salt, LKKL based oligomers and polymers give alpha-helical spectra. These data provide evidence of aggregation induced secondary structure formation in an exceptionally simple peptide system. Similarly, the KL based oligomers and polymers give beta-sheet like spectra at high concentration or at high salt. These systems further provide model systems under "normal" aqueous conditions that yield VCD band shapes that correlate to the major secondary structural types of polypeptides. They are in substantial agreement with those spectra obtained on homopolypeptides and on proteins, confirming the relative independence of the VCD technique from side-chain and solvent effects.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8075391     DOI: 10.1002/bip.360340815

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


  4 in total

1.  Comparison of and limits of accuracy for statistical analyses of vibrational and electronic circular dichroism spectra in terms of correlations to and predictions of protein secondary structure.

Authors:  P Pancoska; E Bitto; V Janota; M Urbanova; V P Gupta; T A Keiderling
Journal:  Protein Sci       Date:  1995-07       Impact factor: 6.725

2.  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

3.  Phosphate-dependent aggregation of [KL]n peptides affects their membranolytic activity.

Authors:  Erik Strandberg; Fabian Schweigardt; Parvesh Wadhwani; Jochen Bürck; Johannes Reichert; Haroldo L P Cravo; Luisa Burger; Anne S Ulrich
Journal:  Sci Rep       Date:  2020-07-23       Impact factor: 4.379

Review 4.  Antibiotic Potential and Biophysical Characterization of Amphipathic β-Stranded [XZ]n Peptides With Alternating Cationic and Hydrophobic Residues.

Authors:  Erik Strandberg; Parvesh Wadhwani; Anne S Ulrich
Journal:  Front Med Technol       Date:  2021-02-04
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.