| Literature DB >> 34386966 |
Luise Franz1,2, Anselm F L Schneider1,2, Christian P R Hackenberger3,4.
Abstract
Proteins conjugated to cyclic cell-penetrating peptides (cCPPs) haAbstractve been shown to be effectively taken up by living cells. Conjugation of proteins to cCPPs in a cleavable manner leads to localization in the cytosol and immediate bioavailability of the protein after uptake. Here we describe how mCherry, a fluorescent protein, can be targeted to a membrane-bound compartment, the nucleus, and a subcellular structure like the actin cytoskeleton after cCPP-mediated uptake into living cells. Targeting peptides are genetically fused to the mCherry protein sequence and the protein is conjugated to the cCPP via a cleavable disulfide bond. Localization of mCherry in the nucleus or the actin skeleton respectively can be observed by live cell confocal fluorescence microscopy.Entities:
Keywords: Cell-penetrating peptides; Cleavable cell-penetrating peptide; Disulfide; Endocytosis-independent protein uptake; Lifeact; Live cell microscopy; Nuclear localization signal; Protein delivery; Transduction
Mesh:
Substances:
Year: 2021 PMID: 34386966 DOI: 10.1007/978-1-0716-1617-8_22
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745