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Intracellular artificial supramolecules based on de novo designed Y15 peptides

De novo designed self-assembling peptides (SAPs) are promising building blocks of supramolecular biomaterials, which can fulfill a wide range of applications, such as scaffolds for tissue culture, three-dimensional cell culture, and vaccine adjuvants. Nevertheless, the use of SAPs in intracellular s...

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Autores principales: Miki, Takayuki, Nakai, Taichi, Hashimoto, Masahiro, Kajiwara, Keigo, Tsutsumi, Hiroshi, Mihara, Hisakazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185068/
https://www.ncbi.nlm.nih.gov/pubmed/34099696
http://dx.doi.org/10.1038/s41467-021-23794-6
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author Miki, Takayuki
Nakai, Taichi
Hashimoto, Masahiro
Kajiwara, Keigo
Tsutsumi, Hiroshi
Mihara, Hisakazu
author_facet Miki, Takayuki
Nakai, Taichi
Hashimoto, Masahiro
Kajiwara, Keigo
Tsutsumi, Hiroshi
Mihara, Hisakazu
author_sort Miki, Takayuki
collection PubMed
description De novo designed self-assembling peptides (SAPs) are promising building blocks of supramolecular biomaterials, which can fulfill a wide range of applications, such as scaffolds for tissue culture, three-dimensional cell culture, and vaccine adjuvants. Nevertheless, the use of SAPs in intracellular spaces has mostly been unexplored. Here, we report a self-assembling peptide, Y15 (YEYKYEYKYEYKYEY), which readily forms β-sheet structures to facilitate bottom-up synthesis of functional protein assemblies in living cells. Superfolder green fluorescent protein (sfGFP) fused to Y15 assembles into fibrils and is observed as fluorescent puncta in mammalian cells. Y15 self-assembly is validated by fluorescence anisotropy and pull-down assays. By using the Y15 platform, we demonstrate intracellular reconstitution of Nck assembly, a Src-homology 2 and 3 domain-containing adaptor protein. The artificial clusters of Nck induce N-WASP (neural Wiskott-Aldrich syndrome protein)-mediated actin polymerization, and the functional importance of Nck domain valency and density is evaluated.
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spelling pubmed-81850682021-06-11 Intracellular artificial supramolecules based on de novo designed Y15 peptides Miki, Takayuki Nakai, Taichi Hashimoto, Masahiro Kajiwara, Keigo Tsutsumi, Hiroshi Mihara, Hisakazu Nat Commun Article De novo designed self-assembling peptides (SAPs) are promising building blocks of supramolecular biomaterials, which can fulfill a wide range of applications, such as scaffolds for tissue culture, three-dimensional cell culture, and vaccine adjuvants. Nevertheless, the use of SAPs in intracellular spaces has mostly been unexplored. Here, we report a self-assembling peptide, Y15 (YEYKYEYKYEYKYEY), which readily forms β-sheet structures to facilitate bottom-up synthesis of functional protein assemblies in living cells. Superfolder green fluorescent protein (sfGFP) fused to Y15 assembles into fibrils and is observed as fluorescent puncta in mammalian cells. Y15 self-assembly is validated by fluorescence anisotropy and pull-down assays. By using the Y15 platform, we demonstrate intracellular reconstitution of Nck assembly, a Src-homology 2 and 3 domain-containing adaptor protein. The artificial clusters of Nck induce N-WASP (neural Wiskott-Aldrich syndrome protein)-mediated actin polymerization, and the functional importance of Nck domain valency and density is evaluated. Nature Publishing Group UK 2021-06-07 /pmc/articles/PMC8185068/ /pubmed/34099696 http://dx.doi.org/10.1038/s41467-021-23794-6 Text en © The Author(s) 2021 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
Miki, Takayuki
Nakai, Taichi
Hashimoto, Masahiro
Kajiwara, Keigo
Tsutsumi, Hiroshi
Mihara, Hisakazu
Intracellular artificial supramolecules based on de novo designed Y15 peptides
title Intracellular artificial supramolecules based on de novo designed Y15 peptides
title_full Intracellular artificial supramolecules based on de novo designed Y15 peptides
title_fullStr Intracellular artificial supramolecules based on de novo designed Y15 peptides
title_full_unstemmed Intracellular artificial supramolecules based on de novo designed Y15 peptides
title_short Intracellular artificial supramolecules based on de novo designed Y15 peptides
title_sort intracellular artificial supramolecules based on de novo designed y15 peptides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185068/
https://www.ncbi.nlm.nih.gov/pubmed/34099696
http://dx.doi.org/10.1038/s41467-021-23794-6
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