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Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems

[Image: see text] Understanding the thermodynamic signature of protein–peptide binding events is a major challenge in computational chemistry. The complexity generated by both components possessing many degrees of freedom poses a significant issue for methods that attempt to directly compute the ent...

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Autores principales: Çınaroğlu, Süleyman Selim, Biggin, Philip C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565830/
https://www.ncbi.nlm.nih.gov/pubmed/37759363
http://dx.doi.org/10.1021/acs.jcim.3c01041
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author Çınaroğlu, Süleyman Selim
Biggin, Philip C.
author_facet Çınaroğlu, Süleyman Selim
Biggin, Philip C.
author_sort Çınaroğlu, Süleyman Selim
collection PubMed
description [Image: see text] Understanding the thermodynamic signature of protein–peptide binding events is a major challenge in computational chemistry. The complexity generated by both components possessing many degrees of freedom poses a significant issue for methods that attempt to directly compute the enthalpic contribution to binding. Indeed, the prevailing assumption has been that the errors associated with such approaches would be too large for them to be meaningful. Nevertheless, we currently have no indication of how well the present methods would perform in terms of predicting the enthalpy of binding for protein–peptide complexes. To that end, we carefully assembled and curated a set of 11 protein–peptide complexes where there is structural and isothermal titration calorimetry data available and then computed the absolute enthalpy of binding. The initial “out of the box” calculations were, as expected, very modest in terms of agreement with the experiment. However, careful inspection of the outliers allows for the identification of key sampling problems such as distinct conformations of peptide termini not being sampled or suboptimal cofactor parameters. Additional simulations guided by these aspects can lead to a respectable correlation with isothermal titration calorimetry (ITC) experiments (R(2) of 0.88 and an RMSE of 1.48 kcal/mol overall). Although one cannot know prospectively whether computed ITC values will be correct or not, this work shows that if experimental ITC data are available, then this in conjunction with computed ITC, can be used as a tool to know if the ensemble being simulated is representative of the true ensemble or not. That is important for allowing the correct interpretation of the detailed dynamics of the system with respect to the measured enthalpy. The results also suggest that computational calorimetry is becoming increasingly feasible. We provide the data set as a resource for the community, which could be used as a benchmark to help further progress in this area.
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spelling pubmed-105658302023-10-12 Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems Çınaroğlu, Süleyman Selim Biggin, Philip C. J Chem Inf Model [Image: see text] Understanding the thermodynamic signature of protein–peptide binding events is a major challenge in computational chemistry. The complexity generated by both components possessing many degrees of freedom poses a significant issue for methods that attempt to directly compute the enthalpic contribution to binding. Indeed, the prevailing assumption has been that the errors associated with such approaches would be too large for them to be meaningful. Nevertheless, we currently have no indication of how well the present methods would perform in terms of predicting the enthalpy of binding for protein–peptide complexes. To that end, we carefully assembled and curated a set of 11 protein–peptide complexes where there is structural and isothermal titration calorimetry data available and then computed the absolute enthalpy of binding. The initial “out of the box” calculations were, as expected, very modest in terms of agreement with the experiment. However, careful inspection of the outliers allows for the identification of key sampling problems such as distinct conformations of peptide termini not being sampled or suboptimal cofactor parameters. Additional simulations guided by these aspects can lead to a respectable correlation with isothermal titration calorimetry (ITC) experiments (R(2) of 0.88 and an RMSE of 1.48 kcal/mol overall). Although one cannot know prospectively whether computed ITC values will be correct or not, this work shows that if experimental ITC data are available, then this in conjunction with computed ITC, can be used as a tool to know if the ensemble being simulated is representative of the true ensemble or not. That is important for allowing the correct interpretation of the detailed dynamics of the system with respect to the measured enthalpy. The results also suggest that computational calorimetry is becoming increasingly feasible. We provide the data set as a resource for the community, which could be used as a benchmark to help further progress in this area. American Chemical Society 2023-09-28 /pmc/articles/PMC10565830/ /pubmed/37759363 http://dx.doi.org/10.1021/acs.jcim.3c01041 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Çınaroğlu, Süleyman Selim
Biggin, Philip C.
Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems
title Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems
title_full Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems
title_fullStr Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems
title_full_unstemmed Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems
title_short Computed Protein–Protein Enthalpy Signatures as a Tool for Identifying Conformation Sampling Problems
title_sort computed protein–protein enthalpy signatures as a tool for identifying conformation sampling problems
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565830/
https://www.ncbi.nlm.nih.gov/pubmed/37759363
http://dx.doi.org/10.1021/acs.jcim.3c01041
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