Estimation of peptide helicity from circular dichroism using the ensemble model

Zavrtanik, Uroš (avtor), Lah, Jurij (avtor), Hadži, San (avtor)

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.

• Jezik: Angleški jezik
• Ključne besede: circular dichroism, helix-coil transition, Lifson-Roig model, helix ellipticity, polylanine alpha-helix folding thermodynamics
• Vrsta gradiva: Članek v reviji
• Tipologija: 1.01 - Izvirni znanstveni članek
• Organizacija: FKKT - Fakulteta za kemijo in kemijsko tehnologijo
• Status publikacije: Objavljeno
• Različica publikacije: Objavljena publikacija
• Leto izida: 2024
• Št. strani: Str. 2652-2663
• Številčenje: Vol. 128, iss. 11
• PID: 20.500.12556/RUL-155243
• UDK: 577.322
• ISSN pri članku: 1520-6106
• DOI: 10.1021/acs.jpcb.3c07511
• COBISS.SI-ID: 189763843
• Datum objave v RUL: 21.03.2024

Gradivo je del revije

• Naslov: The journal of physical chemistry : Condensed matter, materials, surfaces, interfaces & biophysical
• Skrajšan naslov: J. phys. chem., B Condens. mater. surf. interfaces biophys.
• Založnik: American Chemical Society
• ISSN: 1520-6106
• COBISS.SI-ID: 14241063

Licence

• Licenca: CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
• Povezava: http://creativecommons.org/licenses/by/4.0/deed.sl
• Opis: To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

• Jezik: Slovenski jezik
• Ključne besede: cirkularni dikroizem, prehod vijačnica-naključni klobčič, Lifson-Roigov model, eliptičnost alfa-vijačnice, termodinamika zvitja

Projekti

• Financer: ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
• Številka projekta: P1-0201
• Naslov: Fizikalna kemija

• Financer: ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
• Številka projekta: J1-50026
• Naslov: Vloga novega sekvenčnega motiva bogatega z alanini pri kondenzaciji RNA-vezavnih proteinov