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Protlego: a Python package for the analysis and design of chimeric proteins
MOTIVATION: Duplication and recombination of protein fragments have led to the highly diverse protein space that we observe today. By mimicking this natural process, the design of protein chimeras via fragment recombination has proven experimentally successful and has opened a new era for the design...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504633/ https://www.ncbi.nlm.nih.gov/pubmed/33901273 http://dx.doi.org/10.1093/bioinformatics/btab253 |
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author | Ferruz, Noelia Noske, Jakob Höcker, Birte |
author_facet | Ferruz, Noelia Noske, Jakob Höcker, Birte |
author_sort | Ferruz, Noelia |
collection | PubMed |
description | MOTIVATION: Duplication and recombination of protein fragments have led to the highly diverse protein space that we observe today. By mimicking this natural process, the design of protein chimeras via fragment recombination has proven experimentally successful and has opened a new era for the design of customizable proteins. The in silico building of structural models for these chimeric proteins, however, remains a manual task that requires a considerable degree of expertise and is not amenable for high-throughput studies. Energetic and structural analysis of the designed proteins often require the use of several tools, each with their unique technical difficulties and available in different programming languages or web servers. RESULTS: We implemented a Python package that enables automated, high-throughput design of chimeras and their structural analysis. First, it fetches evolutionarily conserved fragments from a built-in database (also available at fuzzle.uni-bayreuth.de). These relationships can then be represented via networks or further selected for chimera construction via recombination. Designed chimeras or natural proteins are then scored and minimized with the Charmm and Amber forcefields and their diverse structural features can be analyzed at ease. Here, we showcase Protlego’s pipeline by exploring the relationships between the P-loop and Rossmann superfolds, building and characterizing their offspring chimeras. We believe that Protlego provides a powerful new tool for the protein design community. AVAILABILITY AND IMPLEMENTATION: Protlego runs on the Linux platform and is freely available at (https://hoecker-lab.github.io/protlego/) with tutorials and documentation. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-8504633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85046332021-10-13 Protlego: a Python package for the analysis and design of chimeric proteins Ferruz, Noelia Noske, Jakob Höcker, Birte Bioinformatics Original Papers MOTIVATION: Duplication and recombination of protein fragments have led to the highly diverse protein space that we observe today. By mimicking this natural process, the design of protein chimeras via fragment recombination has proven experimentally successful and has opened a new era for the design of customizable proteins. The in silico building of structural models for these chimeric proteins, however, remains a manual task that requires a considerable degree of expertise and is not amenable for high-throughput studies. Energetic and structural analysis of the designed proteins often require the use of several tools, each with their unique technical difficulties and available in different programming languages or web servers. RESULTS: We implemented a Python package that enables automated, high-throughput design of chimeras and their structural analysis. First, it fetches evolutionarily conserved fragments from a built-in database (also available at fuzzle.uni-bayreuth.de). These relationships can then be represented via networks or further selected for chimera construction via recombination. Designed chimeras or natural proteins are then scored and minimized with the Charmm and Amber forcefields and their diverse structural features can be analyzed at ease. Here, we showcase Protlego’s pipeline by exploring the relationships between the P-loop and Rossmann superfolds, building and characterizing their offspring chimeras. We believe that Protlego provides a powerful new tool for the protein design community. AVAILABILITY AND IMPLEMENTATION: Protlego runs on the Linux platform and is freely available at (https://hoecker-lab.github.io/protlego/) with tutorials and documentation. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2021-04-26 /pmc/articles/PMC8504633/ /pubmed/33901273 http://dx.doi.org/10.1093/bioinformatics/btab253 Text en © The Author(s) 2021. Published by Oxford University Press. 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 | Original Papers Ferruz, Noelia Noske, Jakob Höcker, Birte Protlego: a Python package for the analysis and design of chimeric proteins |
title | Protlego: a Python package for the analysis and design of chimeric proteins |
title_full | Protlego: a Python package for the analysis and design of chimeric proteins |
title_fullStr | Protlego: a Python package for the analysis and design of chimeric proteins |
title_full_unstemmed | Protlego: a Python package for the analysis and design of chimeric proteins |
title_short | Protlego: a Python package for the analysis and design of chimeric proteins |
title_sort | protlego: a python package for the analysis and design of chimeric proteins |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504633/ https://www.ncbi.nlm.nih.gov/pubmed/33901273 http://dx.doi.org/10.1093/bioinformatics/btab253 |
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