Intracellular artificial supramolecules based on de novo designed Y15 peptides
説明
<jats:title>Abstract</jats:title><jats:p>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.</jats:p>
収録刊行物
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- Nature Communications
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Nature Communications 12 (1), 3412-, 2021-06-07
Springer Science and Business Media LLC
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キーワード
- Oncogene Proteins
- Science
- Q
- Wiskott-Aldrich Syndrome Protein, Neuronal
- Biocompatible Materials
- Actins
- HEK293 Cells
- Protein Domains
- COS Cells
- Chlorocebus aethiops
- Peptide Biosynthesis, Nucleic Acid-Independent
- Animals
- Humans
- Protein Conformation, beta-Strand
- Protein Multimerization
- Peptides
- Adaptor Proteins, Signal Transducing
詳細情報 詳細情報について
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- CRID
- 1360857593814511360
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- ISSN
- 20411723
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- PubMed
- 34099696
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- 資料種別
- journal article
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- データソース種別
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- Crossref
- KAKEN
- OpenAIRE