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Discovering highly potent antimicrobial peptides with deep generative model HydrAMP
Antimicrobial peptides emerge as compounds that can alleviate the global health hazard of antimicrobial resistance, prompting a need for novel computational approaches to peptide generation. Here, we propose HydrAMP, a conditional variational autoencoder that learns lower-dimensional, continuous rep...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017685/ https://www.ncbi.nlm.nih.gov/pubmed/36922490 http://dx.doi.org/10.1038/s41467-023-36994-z |
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author | Szymczak, Paulina Możejko, Marcin Grzegorzek, Tomasz Jurczak, Radosław Bauer, Marta Neubauer, Damian Sikora, Karol Michalski, Michał Sroka, Jacek Setny, Piotr Kamysz, Wojciech Szczurek, Ewa |
author_facet | Szymczak, Paulina Możejko, Marcin Grzegorzek, Tomasz Jurczak, Radosław Bauer, Marta Neubauer, Damian Sikora, Karol Michalski, Michał Sroka, Jacek Setny, Piotr Kamysz, Wojciech Szczurek, Ewa |
author_sort | Szymczak, Paulina |
collection | PubMed |
description | Antimicrobial peptides emerge as compounds that can alleviate the global health hazard of antimicrobial resistance, prompting a need for novel computational approaches to peptide generation. Here, we propose HydrAMP, a conditional variational autoencoder that learns lower-dimensional, continuous representation of peptides and captures their antimicrobial properties. The model disentangles the learnt representation of a peptide from its antimicrobial conditions and leverages parameter-controlled creativity. HydrAMP is the first model that is directly optimized for diverse tasks, including unconstrained and analogue generation and outperforms other approaches in these tasks. An additional preselection procedure based on ranking of generated peptides and molecular dynamics simulations increases experimental validation rate. Wet-lab experiments on five bacterial strains confirm high activity of nine peptides generated as analogues of clinically relevant prototypes, as well as six analogues of an inactive peptide. HydrAMP enables generation of diverse and potent peptides, making a step towards resolving the antimicrobial resistance crisis. |
format | Online Article Text |
id | pubmed-10017685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100176852023-03-17 Discovering highly potent antimicrobial peptides with deep generative model HydrAMP Szymczak, Paulina Możejko, Marcin Grzegorzek, Tomasz Jurczak, Radosław Bauer, Marta Neubauer, Damian Sikora, Karol Michalski, Michał Sroka, Jacek Setny, Piotr Kamysz, Wojciech Szczurek, Ewa Nat Commun Article Antimicrobial peptides emerge as compounds that can alleviate the global health hazard of antimicrobial resistance, prompting a need for novel computational approaches to peptide generation. Here, we propose HydrAMP, a conditional variational autoencoder that learns lower-dimensional, continuous representation of peptides and captures their antimicrobial properties. The model disentangles the learnt representation of a peptide from its antimicrobial conditions and leverages parameter-controlled creativity. HydrAMP is the first model that is directly optimized for diverse tasks, including unconstrained and analogue generation and outperforms other approaches in these tasks. An additional preselection procedure based on ranking of generated peptides and molecular dynamics simulations increases experimental validation rate. Wet-lab experiments on five bacterial strains confirm high activity of nine peptides generated as analogues of clinically relevant prototypes, as well as six analogues of an inactive peptide. HydrAMP enables generation of diverse and potent peptides, making a step towards resolving the antimicrobial resistance crisis. Nature Publishing Group UK 2023-03-15 /pmc/articles/PMC10017685/ /pubmed/36922490 http://dx.doi.org/10.1038/s41467-023-36994-z Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Szymczak, Paulina Możejko, Marcin Grzegorzek, Tomasz Jurczak, Radosław Bauer, Marta Neubauer, Damian Sikora, Karol Michalski, Michał Sroka, Jacek Setny, Piotr Kamysz, Wojciech Szczurek, Ewa Discovering highly potent antimicrobial peptides with deep generative model HydrAMP |
title | Discovering highly potent antimicrobial peptides with deep generative model HydrAMP |
title_full | Discovering highly potent antimicrobial peptides with deep generative model HydrAMP |
title_fullStr | Discovering highly potent antimicrobial peptides with deep generative model HydrAMP |
title_full_unstemmed | Discovering highly potent antimicrobial peptides with deep generative model HydrAMP |
title_short | Discovering highly potent antimicrobial peptides with deep generative model HydrAMP |
title_sort | discovering highly potent antimicrobial peptides with deep generative model hydramp |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017685/ https://www.ncbi.nlm.nih.gov/pubmed/36922490 http://dx.doi.org/10.1038/s41467-023-36994-z |
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