Contact SCGE




SCGE Consortium Home   |  About SCGE Toolkit   |  Contact Us   |  Citing the Toolkit   |  License  
 
Filters ..
Editors
 AsCas12a (Feldan Therapeutics)
Guide Target Locus
 NKG2A
Guides
 NKG2A
  Delivery Systems
 CM18-PTD4
 S10
 S18
 S85
Models
 NK
Select experimental variable to highlight records on the chart: 
 

Note: Hover over the bars to view additional information

Loading...

Results

Gene_editing_in_vitro_by_various_peptide_variants_delivering_Cas12a_in_NK_cells._
Editing Efficiency
Record Id Condition Editor Model Delivery Target Locus Guide Dosage Editing Efficiency % indel Image
15000000531 S10 AsCas12a (Feldan Therapeutics) NK S10 NKG2A NKG2A 1.33uM Cas12a/2.0uM gRNA/7.5uM Shuttle Peptide
15000000532 S18 AsCas12a (Feldan Therapeutics) NK S18 NKG2A NKG2A 1.33uM Cas12a/2.0uM gRNA/7.5uM Shuttle Peptide
15000000533 S85 AsCas12a (Feldan Therapeutics) NK S85 NKG2A NKG2A 1.33uM Cas12a/2.0uM gRNA/7.5uM Shuttle Peptide
15000000534 CM18-PTD4 AsCas12a (Feldan Therapeutics) NK CM18-PTD4 NKG2A NKG2A 1.33uM Cas12a/2.0uM gRNA/7.5uM Shuttle Peptide

Publication Title
Engineered amphiphilic peptides enable delivery of proteins and CRISPR-associated nucleases to airway epithelia. NCBI

Shuttle peptide design and protein delivery to airway epithelia

Shuttle peptide design and protein delivery to airway epithelia. A) Amino acid sequences of shuttle peptides. Sequences aligned to highlight structural similarities. Cationic residues are highlighted in blue; hydrophobic residues are in gray. Remaining residues are in green. B) Indel% in primary NK cells following Cas12a RNP delivery targeting NKG2A gene with indicated shuttle peptide ([Cas12a]: 1.33 uM; [crRNA]: 2.0 µM). Results quantified 48 h after delivery (mean ± SE; n = 3 independent experiments). C) Shuttle peptide-mediated delivery of nuclear-targeted GFP protein to human airway epithelia (HAE) and tracheal explants. Left panel: Schematic of primary HAE grown at air–liquid interface. ASL: airway surface liquid. Right panel: photomicrograph of well-differentiated primary HAE culture demonstrating pseudostratified columnar epithelium. Hematoxylin and eosin stain, ×40 magnification. D) Efficiency of GFP delivery by different shuttle peptides. Peptides applied at four concentrations (5, 10, 15, or 20 uM); GFP concentrations 10 or 20 uM. Left graph: Cells were transduced with indicated peptide and GFP combinations and GFP quantified by fluorescence reader. Results mean ± SE; n = 4 donors. *P < 0.05, **P < 0.005, ***P < 0.001, by one-way ANOVA with Tukey’s multiple comparison test. Right panels: Representative en face views of epithelial sheets following GFP delivery at the highest peptide:GFP concentration (20 uM:20 uM), ×20 magnification. Formulations were applied for 15 min. E) GFP localization in multiple epithelial cell types following shuttle peptide-mediated delivery. HAEs were transduced for 15 min with GFP protein and S10 peptide. Left panel: confocal image (XZ) shows co-localization of GFP and specific marker of ciliated cells (α-tubulin, red, indicated by white arrows), nonciliated cells (white arrowheads), F-actin (phalloidin stain, gray), nuclei (DAPI, blue). Right panel: co-localization of GFP and goblet cell marker (Muc5AC, red, indicated by white arrowhead), nuclei (DAPI, blue), and F-actin (phalloidin stain, gray). n ≥ 6 different donor epithelia; ×64 magnification. F) Shuttle peptide delivery of GFP to human tracheal explants. S10 (20 uM) and GFP protein (20 uM) applied to tracheal explant for 1 h. Left panel: both ciliated (αtubulin, red, white arrowhead) and non-ciliated (white arrow) cells were transduced. Right panel: non-ciliated goblet cells were transduced (Muc5AC, red, white arrows); ×40 magnification. https://doi.org/10.1038/s41467-019-12922-y