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Analysing the origin of long-range interactions in proteins using lattice models

BACKGROUND: Long-range communication is very common in proteins but the physical basis of this phenomenon remains unclear. In order to gain insight into this problem, we decided to explore whether long-range interactions exist in lattice models of proteins. Lattice models of proteins have proven to...

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Autores principales: Noivirt-Brik, Orly, Unger, Ron, Horovitz, Amnon
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2670300/
https://www.ncbi.nlm.nih.gov/pubmed/19178726
http://dx.doi.org/10.1186/1472-6807-9-4
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author Noivirt-Brik, Orly
Unger, Ron
Horovitz, Amnon
author_facet Noivirt-Brik, Orly
Unger, Ron
Horovitz, Amnon
author_sort Noivirt-Brik, Orly
collection PubMed
description BACKGROUND: Long-range communication is very common in proteins but the physical basis of this phenomenon remains unclear. In order to gain insight into this problem, we decided to explore whether long-range interactions exist in lattice models of proteins. Lattice models of proteins have proven to capture some of the basic properties of real proteins and, thus, can be used for elucidating general principles of protein stability and folding. RESULTS: Using a computational version of double-mutant cycle analysis, we show that long-range interactions emerge in lattice models even though they are not an input feature of them. The coupling energy of both short- and long-range pairwise interactions is found to become more positive (destabilizing) in a linear fashion with increasing 'contact-frequency', an entropic term that corresponds to the fraction of states in the conformational ensemble of the sequence in which the pair of residues is in contact. A mathematical derivation of the linear dependence of the coupling energy on 'contact-frequency' is provided. CONCLUSION: Our work shows how 'contact-frequency' should be taken into account in attempts to stabilize proteins by introducing (or stabilizing) contacts in the native state and/or through 'negative design' of non-native contacts.
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spelling pubmed-26703002009-04-20 Analysing the origin of long-range interactions in proteins using lattice models Noivirt-Brik, Orly Unger, Ron Horovitz, Amnon BMC Struct Biol Research Article BACKGROUND: Long-range communication is very common in proteins but the physical basis of this phenomenon remains unclear. In order to gain insight into this problem, we decided to explore whether long-range interactions exist in lattice models of proteins. Lattice models of proteins have proven to capture some of the basic properties of real proteins and, thus, can be used for elucidating general principles of protein stability and folding. RESULTS: Using a computational version of double-mutant cycle analysis, we show that long-range interactions emerge in lattice models even though they are not an input feature of them. The coupling energy of both short- and long-range pairwise interactions is found to become more positive (destabilizing) in a linear fashion with increasing 'contact-frequency', an entropic term that corresponds to the fraction of states in the conformational ensemble of the sequence in which the pair of residues is in contact. A mathematical derivation of the linear dependence of the coupling energy on 'contact-frequency' is provided. CONCLUSION: Our work shows how 'contact-frequency' should be taken into account in attempts to stabilize proteins by introducing (or stabilizing) contacts in the native state and/or through 'negative design' of non-native contacts. BioMed Central 2009-01-29 /pmc/articles/PMC2670300/ /pubmed/19178726 http://dx.doi.org/10.1186/1472-6807-9-4 Text en Copyright © 2009 Noivirt-Brik et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Noivirt-Brik, Orly
Unger, Ron
Horovitz, Amnon
Analysing the origin of long-range interactions in proteins using lattice models
title Analysing the origin of long-range interactions in proteins using lattice models
title_full Analysing the origin of long-range interactions in proteins using lattice models
title_fullStr Analysing the origin of long-range interactions in proteins using lattice models
title_full_unstemmed Analysing the origin of long-range interactions in proteins using lattice models
title_short Analysing the origin of long-range interactions in proteins using lattice models
title_sort analysing the origin of long-range interactions in proteins using lattice models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2670300/
https://www.ncbi.nlm.nih.gov/pubmed/19178726
http://dx.doi.org/10.1186/1472-6807-9-4
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