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Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas
Proteins, as gifts from nature, provide structure, sequence, and function templates for designing biomaterials. As first reported here, one group of proteins called reflectins and derived peptides were found to present distinct intracellular distribution preferences. Taking their conserved motifs an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986269/ https://www.ncbi.nlm.nih.gov/pubmed/36890909 http://dx.doi.org/10.3389/fbioe.2023.1062769 |
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author | Song, Junyi Liu, Chuanyang Li, Baoshan Liu, Liangcheng Zeng, Ling Ye, Zonghuang Wu, Wenjian Zhu, Lingyun Hu, Biru |
author_facet | Song, Junyi Liu, Chuanyang Li, Baoshan Liu, Liangcheng Zeng, Ling Ye, Zonghuang Wu, Wenjian Zhu, Lingyun Hu, Biru |
author_sort | Song, Junyi |
collection | PubMed |
description | Proteins, as gifts from nature, provide structure, sequence, and function templates for designing biomaterials. As first reported here, one group of proteins called reflectins and derived peptides were found to present distinct intracellular distribution preferences. Taking their conserved motifs and flexible linkers as Lego bricks, a series of reflectin-derivates were designed and expressed in cells. The selective intracellular localization property leaned on an RMs (canonical conserved reflectin motifs)-replication-determined manner, suggesting that these linkers and motifs were constructional fragments and ready-to-use building blocks for synthetic design and construction. A precise spatiotemporal application demo was constructed in the work by integrating RL(Nto2) (as one representative of a synthetic peptide derived from RfA1) into the Tet-on system to effectively transport cargo peptides into nuclei at selective time points. Further, the intracellular localization of RfA1 derivatives was spatiotemporally controllable with a CRY2/CIB1 system. At last, the functional homogeneities of either motifs or linkers were verified, which made them standardized building blocks for synthetic biology. In summary, the work provides a modularized, orthotropic, and well-characterized synthetic-peptide warehouse for precisely regulating the nucleocytoplasmic localization of proteins. |
format | Online Article Text |
id | pubmed-9986269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99862692023-03-07 Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas Song, Junyi Liu, Chuanyang Li, Baoshan Liu, Liangcheng Zeng, Ling Ye, Zonghuang Wu, Wenjian Zhu, Lingyun Hu, Biru Front Bioeng Biotechnol Bioengineering and Biotechnology Proteins, as gifts from nature, provide structure, sequence, and function templates for designing biomaterials. As first reported here, one group of proteins called reflectins and derived peptides were found to present distinct intracellular distribution preferences. Taking their conserved motifs and flexible linkers as Lego bricks, a series of reflectin-derivates were designed and expressed in cells. The selective intracellular localization property leaned on an RMs (canonical conserved reflectin motifs)-replication-determined manner, suggesting that these linkers and motifs were constructional fragments and ready-to-use building blocks for synthetic design and construction. A precise spatiotemporal application demo was constructed in the work by integrating RL(Nto2) (as one representative of a synthetic peptide derived from RfA1) into the Tet-on system to effectively transport cargo peptides into nuclei at selective time points. Further, the intracellular localization of RfA1 derivatives was spatiotemporally controllable with a CRY2/CIB1 system. At last, the functional homogeneities of either motifs or linkers were verified, which made them standardized building blocks for synthetic biology. In summary, the work provides a modularized, orthotropic, and well-characterized synthetic-peptide warehouse for precisely regulating the nucleocytoplasmic localization of proteins. Frontiers Media S.A. 2023-02-20 /pmc/articles/PMC9986269/ /pubmed/36890909 http://dx.doi.org/10.3389/fbioe.2023.1062769 Text en Copyright © 2023 Song, Liu, Li, Liu, Zeng, Ye, Wu, Zhu and Hu. 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 | Bioengineering and Biotechnology Song, Junyi Liu, Chuanyang Li, Baoshan Liu, Liangcheng Zeng, Ling Ye, Zonghuang Wu, Wenjian Zhu, Lingyun Hu, Biru Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas |
title | Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas |
title_full | Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas |
title_fullStr | Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas |
title_full_unstemmed | Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas |
title_short | Synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas |
title_sort | synthetic peptides for the precise transportation of proteins of interests to selectable subcellular areas |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986269/ https://www.ncbi.nlm.nih.gov/pubmed/36890909 http://dx.doi.org/10.3389/fbioe.2023.1062769 |
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