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A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design
Protein-protein interactions (PPIs) are crucial for biological functions and have applications ranging from drug design to synthetic cell circuits. Coiled-coils have been used as a model to study the sequence determinants of specificity. However, building well-behaved sets of orthogonal pairs of coi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397247/ https://www.ncbi.nlm.nih.gov/pubmed/37532706 http://dx.doi.org/10.1038/s41467-023-38697-x |
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author | Boldridge, W. Clifford Ljubetič, Ajasja Kim, Hwangbeom Lubock, Nathan Szilágyi, Dániel Lee, Jonathan Brodnik, Andrej Jerala, Roman Kosuri, Sriram |
author_facet | Boldridge, W. Clifford Ljubetič, Ajasja Kim, Hwangbeom Lubock, Nathan Szilágyi, Dániel Lee, Jonathan Brodnik, Andrej Jerala, Roman Kosuri, Sriram |
author_sort | Boldridge, W. Clifford |
collection | PubMed |
description | Protein-protein interactions (PPIs) are crucial for biological functions and have applications ranging from drug design to synthetic cell circuits. Coiled-coils have been used as a model to study the sequence determinants of specificity. However, building well-behaved sets of orthogonal pairs of coiled-coils remains challenging due to inaccurate predictions of orthogonality and difficulties in testing at scale. To address this, we develop the next-generation bacterial two-hybrid (NGB2H) method, which allows for the rapid exploration of interactions of programmed protein libraries in a quantitative and scalable way using next-generation sequencing readout. We design, build, and test large sets of orthogonal synthetic coiled-coils, assayed over 8,000 PPIs, and used the dataset to train a more accurate coiled-coil scoring algorithm (iCipa). After characterizing nearly 18,000 new PPIs, we identify to the best of our knowledge the largest set of orthogonal coiled-coils to date, with fifteen on-target interactions. Our approach provides a powerful tool for the design of orthogonal PPIs. |
format | Online Article Text |
id | pubmed-10397247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103972472023-08-04 A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design Boldridge, W. Clifford Ljubetič, Ajasja Kim, Hwangbeom Lubock, Nathan Szilágyi, Dániel Lee, Jonathan Brodnik, Andrej Jerala, Roman Kosuri, Sriram Nat Commun Article Protein-protein interactions (PPIs) are crucial for biological functions and have applications ranging from drug design to synthetic cell circuits. Coiled-coils have been used as a model to study the sequence determinants of specificity. However, building well-behaved sets of orthogonal pairs of coiled-coils remains challenging due to inaccurate predictions of orthogonality and difficulties in testing at scale. To address this, we develop the next-generation bacterial two-hybrid (NGB2H) method, which allows for the rapid exploration of interactions of programmed protein libraries in a quantitative and scalable way using next-generation sequencing readout. We design, build, and test large sets of orthogonal synthetic coiled-coils, assayed over 8,000 PPIs, and used the dataset to train a more accurate coiled-coil scoring algorithm (iCipa). After characterizing nearly 18,000 new PPIs, we identify to the best of our knowledge the largest set of orthogonal coiled-coils to date, with fifteen on-target interactions. Our approach provides a powerful tool for the design of orthogonal PPIs. Nature Publishing Group UK 2023-08-02 /pmc/articles/PMC10397247/ /pubmed/37532706 http://dx.doi.org/10.1038/s41467-023-38697-x Text en © The Author(s) 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 Boldridge, W. Clifford Ljubetič, Ajasja Kim, Hwangbeom Lubock, Nathan Szilágyi, Dániel Lee, Jonathan Brodnik, Andrej Jerala, Roman Kosuri, Sriram A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design |
title | A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design |
title_full | A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design |
title_fullStr | A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design |
title_full_unstemmed | A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design |
title_short | A multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design |
title_sort | multiplexed bacterial two-hybrid for rapid characterization of protein–protein interactions and iterative protein design |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397247/ https://www.ncbi.nlm.nih.gov/pubmed/37532706 http://dx.doi.org/10.1038/s41467-023-38697-x |
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