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iCFN: an efficient exact algorithm for multistate protein design

MOTIVATION: Multistate protein design addresses real-world challenges, such as multi-specificity design and backbone flexibility, by considering both positive and negative protein states with an ensemble of substates for each. It also presents an enormous challenge to exact algorithms that guarantee...

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Detalles Bibliográficos
Autores principales: Karimi, Mostafa, Shen, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129278/
https://www.ncbi.nlm.nih.gov/pubmed/30423073
http://dx.doi.org/10.1093/bioinformatics/bty564
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author Karimi, Mostafa
Shen, Yang
author_facet Karimi, Mostafa
Shen, Yang
author_sort Karimi, Mostafa
collection PubMed
description MOTIVATION: Multistate protein design addresses real-world challenges, such as multi-specificity design and backbone flexibility, by considering both positive and negative protein states with an ensemble of substates for each. It also presents an enormous challenge to exact algorithms that guarantee the optimal solutions and enable a direct test of mechanistic hypotheses behind models. However, efficient exact algorithms are lacking for multistate protein design. RESULTS: We have developed an efficient exact algorithm called interconnected cost function networks (iCFN) for multistate protein design. Its generic formulation allows for a wide array of applications such as stability, affinity and specificity designs while addressing concerns such as global flexibility of protein backbones. iCFN treats each substate design as a weighted constraint satisfaction problem (WCSP) modeled through a CFN; and it solves the coupled WCSPs using novel bounds and a depth-first branch-and-bound search over a tree structure of sequences, substates, and conformations. When iCFN is applied to specificity design of a T-cell receptor, a problem of unprecedented size to exact methods, it drastically reduces search space and running time to make the problem tractable. Moreover, iCFN generates experimentally-agreeing receptor designs with improved accuracy compared with state-of-the-art methods, highlights the importance of modeling backbone flexibility in protein design, and reveals molecular mechanisms underlying binding specificity. AVAILABILITY AND IMPLEMENTATION: https://shen-lab.github.io/software/iCFN SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-61292782018-09-12 iCFN: an efficient exact algorithm for multistate protein design Karimi, Mostafa Shen, Yang Bioinformatics Eccb 2018: European Conference on Computational Biology Proceedings MOTIVATION: Multistate protein design addresses real-world challenges, such as multi-specificity design and backbone flexibility, by considering both positive and negative protein states with an ensemble of substates for each. It also presents an enormous challenge to exact algorithms that guarantee the optimal solutions and enable a direct test of mechanistic hypotheses behind models. However, efficient exact algorithms are lacking for multistate protein design. RESULTS: We have developed an efficient exact algorithm called interconnected cost function networks (iCFN) for multistate protein design. Its generic formulation allows for a wide array of applications such as stability, affinity and specificity designs while addressing concerns such as global flexibility of protein backbones. iCFN treats each substate design as a weighted constraint satisfaction problem (WCSP) modeled through a CFN; and it solves the coupled WCSPs using novel bounds and a depth-first branch-and-bound search over a tree structure of sequences, substates, and conformations. When iCFN is applied to specificity design of a T-cell receptor, a problem of unprecedented size to exact methods, it drastically reduces search space and running time to make the problem tractable. Moreover, iCFN generates experimentally-agreeing receptor designs with improved accuracy compared with state-of-the-art methods, highlights the importance of modeling backbone flexibility in protein design, and reveals molecular mechanisms underlying binding specificity. AVAILABILITY AND IMPLEMENTATION: https://shen-lab.github.io/software/iCFN SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2018-09-01 2018-09-08 /pmc/articles/PMC6129278/ /pubmed/30423073 http://dx.doi.org/10.1093/bioinformatics/bty564 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Eccb 2018: European Conference on Computational Biology Proceedings
Karimi, Mostafa
Shen, Yang
iCFN: an efficient exact algorithm for multistate protein design
title iCFN: an efficient exact algorithm for multistate protein design
title_full iCFN: an efficient exact algorithm for multistate protein design
title_fullStr iCFN: an efficient exact algorithm for multistate protein design
title_full_unstemmed iCFN: an efficient exact algorithm for multistate protein design
title_short iCFN: an efficient exact algorithm for multistate protein design
title_sort icfn: an efficient exact algorithm for multistate protein design
topic Eccb 2018: European Conference on Computational Biology Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129278/
https://www.ncbi.nlm.nih.gov/pubmed/30423073
http://dx.doi.org/10.1093/bioinformatics/bty564
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