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NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning
Antibodies are a rapidly growing class of therapeutics. Recently, single domain camelid VHH antibodies, and their recognition nanobody domain (Nb) appeared as a cost-effective highly stable alternative to full-length antibodies. There is a growing need for high-throughput epitope mapping based on ac...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411858/ https://www.ncbi.nlm.nih.gov/pubmed/36032123 http://dx.doi.org/10.3389/fimmu.2022.958584 |
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author | Cohen, Tomer Halfon, Matan Schneidman-Duhovny, Dina |
author_facet | Cohen, Tomer Halfon, Matan Schneidman-Duhovny, Dina |
author_sort | Cohen, Tomer |
collection | PubMed |
description | Antibodies are a rapidly growing class of therapeutics. Recently, single domain camelid VHH antibodies, and their recognition nanobody domain (Nb) appeared as a cost-effective highly stable alternative to full-length antibodies. There is a growing need for high-throughput epitope mapping based on accurate structural modeling of the variable domains that share a common fold and differ in the Complementarity Determining Regions (CDRs). We develop a deep learning end-to-end model, NanoNet, that given a sequence directly produces the 3D coordinates of the backbone and Cβ atoms of the entire VH domain. For the Nb test set, NanoNet achieves 3.16Å average RMSD for the most variable CDR3 loops and 2.65Å, 1.73Å for the CDR1, CDR2 loops, respectively. The accuracy for antibody VH domains is even higher: 2.38Å RMSD for CDR3 and 0.89Å, 0.96Å for the CDR1, CDR2 loops, respectively. NanoNet run times allow generation of ∼1M nanobody structures in less than 4 hours on a standard CPU computer enabling high-throughput structure modeling. NanoNet is available at GitHub: https://github.com/dina-lab3D/NanoNet |
format | Online Article Text |
id | pubmed-9411858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94118582022-08-27 NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning Cohen, Tomer Halfon, Matan Schneidman-Duhovny, Dina Front Immunol Immunology Antibodies are a rapidly growing class of therapeutics. Recently, single domain camelid VHH antibodies, and their recognition nanobody domain (Nb) appeared as a cost-effective highly stable alternative to full-length antibodies. There is a growing need for high-throughput epitope mapping based on accurate structural modeling of the variable domains that share a common fold and differ in the Complementarity Determining Regions (CDRs). We develop a deep learning end-to-end model, NanoNet, that given a sequence directly produces the 3D coordinates of the backbone and Cβ atoms of the entire VH domain. For the Nb test set, NanoNet achieves 3.16Å average RMSD for the most variable CDR3 loops and 2.65Å, 1.73Å for the CDR1, CDR2 loops, respectively. The accuracy for antibody VH domains is even higher: 2.38Å RMSD for CDR3 and 0.89Å, 0.96Å for the CDR1, CDR2 loops, respectively. NanoNet run times allow generation of ∼1M nanobody structures in less than 4 hours on a standard CPU computer enabling high-throughput structure modeling. NanoNet is available at GitHub: https://github.com/dina-lab3D/NanoNet Frontiers Media S.A. 2022-08-12 /pmc/articles/PMC9411858/ /pubmed/36032123 http://dx.doi.org/10.3389/fimmu.2022.958584 Text en Copyright © 2022 Cohen, Halfon and Schneidman-Duhovny https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Cohen, Tomer Halfon, Matan Schneidman-Duhovny, Dina NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning |
title | NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning |
title_full | NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning |
title_fullStr | NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning |
title_full_unstemmed | NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning |
title_short | NanoNet: Rapid and accurate end-to-end nanobody modeling by deep learning |
title_sort | nanonet: rapid and accurate end-to-end nanobody modeling by deep learning |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411858/ https://www.ncbi.nlm.nih.gov/pubmed/36032123 http://dx.doi.org/10.3389/fimmu.2022.958584 |
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