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Estimation of peptide helicity from circular dichroism using the ensemble model
ID Zavrtanik, Uroš (Author), ID Lah, Jurij (Author), ID Hadži, San (Author)

URLURL - Source URL, Visit https://pubs.acs.org/doi/10.1021/acs.jpcb.3c07511 This link opens in a new window
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Abstract
An established method for the quantitation of the helix content in peptides using circular dichroism (CD) relies on the linear spectroscopic model. This model assumes an average value of the helix-length correction for all peptide conformers, irrespective of the length of the helical segment. Here we assess the validity of this approximation and introduce a more physically realistic ensemble-based analysis of the CD signal in which the length correction is assigned specifically to each ensemble conformer. We demonstrate that the linear model underestimates peptide helicity, with the difference depending on the ensemble composition. We developed a computer program that implements the ensemble model to estimate the peptide helicity. Using this model and the CD data set covering a broad range of helicities, we recalibrate CD baseline parameters and redetermine helix–coil parameters for the alanine-rich peptide. We show that the ensemble model leverages small differences in signal between conformers to extract more information from the experimental data, enabling the determination of several poorly defined quantities, such as the nucleation constant and heat capacity change associated with helix folding. Overall, the presented ensemble-based treatment of the CD signal, together with the recalibrated values of the spectroscopic baseline parameters, provides a coherent framework for the analysis of the peptide helix content.

Language:English
Keywords:circular dichroism, helix-coil transition, Lifson-Roig model, helix ellipticity, polylanine alpha-helix folding thermodynamics
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Publication status:Published
Publication version:Version of Record
Year:2024
Number of pages:Str. 2652-2663
Numbering:Vol. 128, iss. 11
PID:20.500.12556/RUL-155243 This link opens in a new window
UDC:577.322
ISSN on article:1520-6106
DOI:10.1021/acs.jpcb.3c07511 This link opens in a new window
COBISS.SI-ID:189763843 This link opens in a new window
Publication date in RUL:21.03.2024
Views:87
Downloads:146
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Record is a part of a journal

Title:The journal of physical chemistry : Condensed matter, materials, surfaces, interfaces & biophysical
Shortened title:J. phys. chem., B Condens. mater. surf. interfaces biophys.
Publisher:American Chemical Society
ISSN:1520-6106
COBISS.SI-ID:14241063 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:cirkularni dikroizem, prehod vijačnica-naključni klobčič, Lifson-Roigov model, eliptičnost alfa-vijačnice, termodinamika zvitja

Projects

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0201
Name:Fizikalna kemija

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J1-50026
Name:Vloga novega sekvenčnega motiva bogatega z alanini pri kondenzaciji RNA-vezavnih proteinov

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