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LoopGrafter: a web tool for transplanting dynamical loops for protein engineering
The transplantation of loops between structurally related proteins is a compelling method to improve the activity, specificity and stability of enzymes. However, despite the interest of loop regions in protein engineering, the available methods of loop-based rational protein design are scarce. One p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252738/ https://www.ncbi.nlm.nih.gov/pubmed/35438789 http://dx.doi.org/10.1093/nar/gkac249 |
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author | Planas-Iglesias, Joan Opaleny, Filip Ulbrich, Pavol Stourac, Jan Sanusi, Zainab Pinto, Gaspar P Schenkmayerova, Andrea Byska, Jan Damborsky, Jiri Kozlikova, Barbora Bednar, David |
author_facet | Planas-Iglesias, Joan Opaleny, Filip Ulbrich, Pavol Stourac, Jan Sanusi, Zainab Pinto, Gaspar P Schenkmayerova, Andrea Byska, Jan Damborsky, Jiri Kozlikova, Barbora Bednar, David |
author_sort | Planas-Iglesias, Joan |
collection | PubMed |
description | The transplantation of loops between structurally related proteins is a compelling method to improve the activity, specificity and stability of enzymes. However, despite the interest of loop regions in protein engineering, the available methods of loop-based rational protein design are scarce. One particular difficulty related to loop engineering is the unique dynamism that enables them to exert allosteric control over the catalytic function of enzymes. Thus, when engaging in a transplantation effort, such dynamics in the context of protein structure need consideration. A second practical challenge is identifying successful excision points for the transplantation or grafting. Here, we present LoopGrafter (https://loschmidt.chemi.muni.cz/loopgrafter/), a web server that specifically guides in the loop grafting process between structurally related proteins. The server provides a step-by-step interactive procedure in which the user can successively identify loops in the two input proteins, calculate their geometries, assess their similarities and dynamics, and select a number of loops to be transplanted. All possible different chimeric proteins derived from any existing recombination point are calculated, and 3D models for each of them are constructed and energetically evaluated. The obtained results can be interactively visualized in a user-friendly graphical interface and downloaded for detailed structural analyses. |
format | Online Article Text |
id | pubmed-9252738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92527382022-07-05 LoopGrafter: a web tool for transplanting dynamical loops for protein engineering Planas-Iglesias, Joan Opaleny, Filip Ulbrich, Pavol Stourac, Jan Sanusi, Zainab Pinto, Gaspar P Schenkmayerova, Andrea Byska, Jan Damborsky, Jiri Kozlikova, Barbora Bednar, David Nucleic Acids Res Web Server Issue The transplantation of loops between structurally related proteins is a compelling method to improve the activity, specificity and stability of enzymes. However, despite the interest of loop regions in protein engineering, the available methods of loop-based rational protein design are scarce. One particular difficulty related to loop engineering is the unique dynamism that enables them to exert allosteric control over the catalytic function of enzymes. Thus, when engaging in a transplantation effort, such dynamics in the context of protein structure need consideration. A second practical challenge is identifying successful excision points for the transplantation or grafting. Here, we present LoopGrafter (https://loschmidt.chemi.muni.cz/loopgrafter/), a web server that specifically guides in the loop grafting process between structurally related proteins. The server provides a step-by-step interactive procedure in which the user can successively identify loops in the two input proteins, calculate their geometries, assess their similarities and dynamics, and select a number of loops to be transplanted. All possible different chimeric proteins derived from any existing recombination point are calculated, and 3D models for each of them are constructed and energetically evaluated. The obtained results can be interactively visualized in a user-friendly graphical interface and downloaded for detailed structural analyses. Oxford University Press 2022-04-19 /pmc/articles/PMC9252738/ /pubmed/35438789 http://dx.doi.org/10.1093/nar/gkac249 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Web Server Issue Planas-Iglesias, Joan Opaleny, Filip Ulbrich, Pavol Stourac, Jan Sanusi, Zainab Pinto, Gaspar P Schenkmayerova, Andrea Byska, Jan Damborsky, Jiri Kozlikova, Barbora Bednar, David LoopGrafter: a web tool for transplanting dynamical loops for protein engineering |
title | LoopGrafter: a web tool for transplanting dynamical loops for protein engineering |
title_full | LoopGrafter: a web tool for transplanting dynamical loops for protein engineering |
title_fullStr | LoopGrafter: a web tool for transplanting dynamical loops for protein engineering |
title_full_unstemmed | LoopGrafter: a web tool for transplanting dynamical loops for protein engineering |
title_short | LoopGrafter: a web tool for transplanting dynamical loops for protein engineering |
title_sort | loopgrafter: a web tool for transplanting dynamical loops for protein engineering |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252738/ https://www.ncbi.nlm.nih.gov/pubmed/35438789 http://dx.doi.org/10.1093/nar/gkac249 |
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