論文

基本情報

氏名 二見 翠
氏名(カナ) フタミ ミドリ
氏名(英語) Futami Midori
所属 生命科学部 生物科学科
職名 准教授
researchmap研究者コード B000345493
researchmap機関 岡山理科大学

題名

Enhanced in-cell folding of reversibly cationized transcription factor using amphipathic peptide.

単著・共著の別

著者

Futami M, Nakano T, Yasunaga M, Makihara M, Asama T, Hagihara Y, Nakajima Y, Futami J

概要

Protein transduction; Cell-permeable peptide; In-cell folding; Amphipathic peptide; Chemical modification
The intracellular delivery of functionally active transcription factor proteins is emerging as a promising technique for artificial regulation of cellular functions. However, in addition to the cell membrane, which acts as a barrier to macromolecules, the aggregation-favored properties of structurally flexible transcription factor proteins limit the application of this method. In-cell folding technique can be used to overcome these issues. This technique solubilizes denatured protein by reversible alkyl-disulfide cationization (S-cationization), and simultaneously endows efficient intracellular delivery and folding to the biologically active conformation in the reducing environment of the cytosol. Because cationized protein is internalized into cells by adsorption-mediated endocytosis, endosomal escape is crucial for this technique. In this study, we utilized a sensitive luciferase reporter gene assay to quantitatively evaluate in-cell folding of the artificial transcription factor GAL4-VP16. Although the cationic moiety of S-cationized protein was slightly affected, co-transduction of amphipathic peptide Endo-PORTER dramatically improved in-cell folding efficiency. Live cell imaging of fluorescent-labeled GAL4-VP16 revealed that some of the proteins diffused into the cytosol and nucleus through co-transduction with Endo-PORTER. Real-time monitoring of light output of luciferase revealed the kinetics of in-cell folding, supporting that endosomal-release assisted by Endo-PORTER was stimulated by endosome acidification. Because this method can transduce proteins uniformly and repeatedly into living cells, S-cationized transcription factor proteins are widely applicable for the artificial regulation of cellular functions.


発表雑誌等の名称

J Biosci Bioeng

出版者

123

4

開始ページ

419

終了ページ

424

発行又は発表の年月

2017/04

査読の有無

有り

招待の有無

記述言語

英語

掲載種別

研究論文(学術雑誌)

ISSN

ID:DOI

ID:NAID(CiNiiのID)

ID:PMID

URL

JGlobalID

arXiv ID

ORCIDのPut Code

DBLP ID