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An integrative characterization of proline cis and trans conformers in a disordered peptide

Pettitt, AJ; Shukla, VK; Figueiredo, AM; Newton, LS; McCarthy, S; Tabor, AB; Heller, GT; ... Hansen, DF; + view all (2024) An integrative characterization of proline cis and trans conformers in a disordered peptide. Biophysical Journal , 123 (21) pp. 3798-3811. 10.1016/j.bpj.2024.09.028. Green open access

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Abstract

Intrinsically disordered proteins (IDPs) often contain proline residues that undergo cis/trans isomerization. While molecular dynamics (MD) simulations have the potential to fully characterize the proline cis and trans subensembles, they are limited by the slow timescales of isomerization and force field inaccuracies. NMR spectroscopy can report on ensemble-averaged observables for both the cis-proline and trans-proline states, but a full atomistic characterization of these conformers is challenging. Given the importance of proline cis/trans isomerization for influencing the conformational sampling of disordered proteins, we employed a combination of all-atom MD simulations with enhanced sampling (metadynamics), NMR, and small-angle x-ray scattering (SAXS) to characterize the two subensembles of the ORF6 C-terminal region (ORF6CTR) from SARS-CoV-2 corresponding to the proline-57 (P57) cis and trans states. We performed MD simulations in three distinct force fields: AMBER03ws, AMBER99SB-disp, and CHARMM36m, which are all optimized for disordered proteins. Each simulation was run for an accumulated time of 180–220 μs until convergence was reached, as assessed by blocking analysis. A good agreement between the cis-P57 populations predicted from metadynamic simulations in AMBER03ws was observed with populations obtained from experimental NMR data. Moreover, we observed good agreement between the radius of gyration predicted from the metadynamic simulations in AMBER03ws and that measured using SAXS. Our findings suggest that both the cis-P57 and trans-P57 conformations of ORF6CTR are extremely dynamic and that interdisciplinary approaches combining both multiscale computations and experiments offer avenues to explore highly dynamic states that cannot be reliably characterized by either approach in isolation.

Type: Article
Title: An integrative characterization of proline cis and trans conformers in a disordered peptide
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.bpj.2024.09.028
Publisher version: http://dx.doi.org/10.1016/j.bpj.2024.09.028
Language: English
Additional information: © 2024 The Author(s). Published by Elsevier Inc. on behalf of Biophysical Society. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Keywords: Proline, Molecular Dynamics Simulation, Scattering, Small Angle, Protein Conformation, Intrinsically Disordered Proteins, X-Ray Diffraction, Peptides, Isomerism, SARS-CoV-2, Viral Proteins
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Infection and Immunity
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences > Structural and Molecular Biology
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry
URI: https://discovery.ucl.ac.uk/id/eprint/10201124
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