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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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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. |
format | Online Article Text |
id | pubmed-6129278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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