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

Author:
Futami, Midori, Nakano, Tomoki, Yasunaga, Mayu, Makihara, Masahiro, Asama, Takashi, Hagihara, Yoshihisa, Nakajima, Yoshihiro, Futami, Junichiro
Source:
Journal of bioscience and bioengineering 2017 v.123 no.4 pp. 419-424
ISSN:
1389-1723
Subject:
acidification, cell membranes, cytosol, endocytosis, image analysis, luciferase, monitoring, reporter genes, transcription factors
Abstract:
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.
Agid:
5605898