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The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity
Genetically-encoded combinatorial peptide libraries are convenient tools to identify peptides to be used as therapeutics, antimicrobials and functional synthetic biology modules. Here, we report the identification and characterization of a cyclic peptide, G4CP2, that interferes with the GAL4 protein...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014601/ https://www.ncbi.nlm.nih.gov/pubmed/36936986 http://dx.doi.org/10.3389/fmolb.2023.1017757 |
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author | Rosa, Stefano Tagliani, Andrea Bertaso, Chiara Tadini, Luca Visentin, Cristina Gourlay, Louise Jane Pricl, Sabrina Feni, Lucia Pellegrino, Sara Pesaresi, Paolo Masiero, Simona |
author_facet | Rosa, Stefano Tagliani, Andrea Bertaso, Chiara Tadini, Luca Visentin, Cristina Gourlay, Louise Jane Pricl, Sabrina Feni, Lucia Pellegrino, Sara Pesaresi, Paolo Masiero, Simona |
author_sort | Rosa, Stefano |
collection | PubMed |
description | Genetically-encoded combinatorial peptide libraries are convenient tools to identify peptides to be used as therapeutics, antimicrobials and functional synthetic biology modules. Here, we report the identification and characterization of a cyclic peptide, G4CP2, that interferes with the GAL4 protein, a transcription factor responsible for the activation of galactose catabolism in yeast and widely exploited in molecular biology. G4CP2 was identified by screening CYCLIC, a Yeast Two-Hybrid-based combinatorial library of cyclic peptides developed in our laboratory. G4CP2 interferes with GAL4-mediated activation of galactose metabolic enzymes both when expressed intracellularly, as a recombinant peptide, and when provided exogenously, as a chemically-synthesized cyclic peptide. Our results support the application of G4CP2 in microbial biotechnology and, additionally, demonstrate that CYCLIC can be used as a tool for the rapid identification of peptides, virtually without any limitations with respect to the target protein. The possible biotechnological applications of cyclic peptides are also discussed. |
format | Online Article Text |
id | pubmed-10014601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100146012023-03-16 The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity Rosa, Stefano Tagliani, Andrea Bertaso, Chiara Tadini, Luca Visentin, Cristina Gourlay, Louise Jane Pricl, Sabrina Feni, Lucia Pellegrino, Sara Pesaresi, Paolo Masiero, Simona Front Mol Biosci Molecular Biosciences Genetically-encoded combinatorial peptide libraries are convenient tools to identify peptides to be used as therapeutics, antimicrobials and functional synthetic biology modules. Here, we report the identification and characterization of a cyclic peptide, G4CP2, that interferes with the GAL4 protein, a transcription factor responsible for the activation of galactose catabolism in yeast and widely exploited in molecular biology. G4CP2 was identified by screening CYCLIC, a Yeast Two-Hybrid-based combinatorial library of cyclic peptides developed in our laboratory. G4CP2 interferes with GAL4-mediated activation of galactose metabolic enzymes both when expressed intracellularly, as a recombinant peptide, and when provided exogenously, as a chemically-synthesized cyclic peptide. Our results support the application of G4CP2 in microbial biotechnology and, additionally, demonstrate that CYCLIC can be used as a tool for the rapid identification of peptides, virtually without any limitations with respect to the target protein. The possible biotechnological applications of cyclic peptides are also discussed. Frontiers Media S.A. 2023-03-01 /pmc/articles/PMC10014601/ /pubmed/36936986 http://dx.doi.org/10.3389/fmolb.2023.1017757 Text en Copyright © 2023 Rosa, Tagliani, Bertaso, Tadini, Visentin, Gourlay, Pricl, Feni, Pellegrino, Pesaresi and Masiero. 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 | Molecular Biosciences Rosa, Stefano Tagliani, Andrea Bertaso, Chiara Tadini, Luca Visentin, Cristina Gourlay, Louise Jane Pricl, Sabrina Feni, Lucia Pellegrino, Sara Pesaresi, Paolo Masiero, Simona The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity |
title | The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity |
title_full | The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity |
title_fullStr | The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity |
title_full_unstemmed | The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity |
title_short | The cyclic peptide G4CP2 enables the modulation of galactose metabolism in yeast by interfering with GAL4 transcriptional activity |
title_sort | cyclic peptide g4cp2 enables the modulation of galactose metabolism in yeast by interfering with gal4 transcriptional activity |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014601/ https://www.ncbi.nlm.nih.gov/pubmed/36936986 http://dx.doi.org/10.3389/fmolb.2023.1017757 |
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