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https://pubs.rsc.org/en/content/articlelanding/2008/ob/b809006h
Non-covalent delivery of proteins into mammalian cells - Organic & Biomolecular Chemistry (RSC Publishing) Substances that mediate the import of proteins into cells, “carriers”, have many potential applications. The most potentially useful carriers do not have to be covalently linked to their protein …Author: Aurore Loudet, Junyan Han, Rola Barhoumi, Jean-Philippe Pellois, Robert C. Burghardt, Kevin Burgess
https://www.researchgate.net/publication/23503129_Non-covalent_delivery_of_proteins_into_mammalian_cells
Non-covalent delivery of proteins into mammalian cells. Substances that mediate the import of proteins into cells, "carriers", have many potential applications. The most potentially useful carriers do not have to be covalently linked to their protein cargoes.
https://www.academia.edu/32353241/Non-covalent_delivery_of_proteins_into_mammalian_cells
Non-covalent delivery of proteins into mammalian cells
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924640/
Aug 20, 2010 · We hypothesized that +36 GFP may also serve as a potent and general platform for the delivery of proteins into mammalian cells. We began by generating a variety of fusion proteins with +36 GFP and observed that these fusions maintain the ability to rapidly (within 15 min) and potently (at low nanomolar concentrations) penetrate mammalian cells without toxicity ( Supplementary Figures …Author: James J. Cronican, David B. Thompson, Kevin T. Beier, Brian R. McNaughton, Connie Cepko, David Ruchi...
https://www.sciencedirect.com/science/article/pii/S138917230570339X
Proteins adhering to the cell surface will accordingly also become internalized into cells and end up in lysosome and other intracellular vesicles. Recent reports have shown that the protein transduction domains or cell penetrating peptides also mediate cell surface adhesion followed by internalization into cells by endocytosis (13, 14). Therefore, enhancement of the ionic charge interaction seems to be a reasonable strategy to increase the adsorption-mediated delivery of a protein into ...Author: Junichiro Futami, Midori Kitazoe, Takashi Maeda, Emiko Nukui, Masakiyo Sakaguchi, Jun Kosaka, Masahi...
https://pubs.acs.org/doi/10.1021/cb1001153
Delivery of mCherry into cells by +36 GFP was confirmed by live-cell confocal fluorescence microscopy (Figure 1, panel b) and by comparison with control experiments in which endocytosis is blocked at 4 °C and protein remains surface-bound (Supplementary Figure 6).Author: James J. Cronican, David B. Thompson, Kevin T. Beier, Brian R. McNaughton, Connie Cepko, David Ruchi...
https://www.nature.com/articles/nbt.3081
Oct 30, 2014 · Figure 1: Strategy for delivering proteins into mammalian cells by fusion or noncovalent complexation with polyanionic macromolecules and complexation with cationic lipids. Figure 2: Delivery …Author: John A. Zuris, John A. Zuris, David B. Thompson, David B. Thompson, Yilai Shu, John P. Guilinger, Jo...
https://www.nature.com/articles/nbt1201-1173
Dec 01, 2001 · For Pep-1-mediated delivery of proteins and peptides, Pep-1/protein or Pep-1/peptide complexes were formed in DMEM or PBS (500 μl of DMEM containing 0.25 μg of protein or peptide and a variable Pep-1:protein molecular ratio from 1:1 to 40:1) and incubated for 30 min at 37°C.Author: May C. Morris, Julien Depollier, Jean Mery, Frederic Heitz, Gilles Divita
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