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EXP001412

Paper

Calcium condensed cell penetrating peptide complexes offer highly efficient, low toxicity gene silencing (2012)

Peptide

TAT

Sequence: Stearyl-AGYLLGKLLOOLAAAALOOLL-NH2

RNA

siRNA

All experiment fields

Experiment Id EXP001412
Paper Calcium condensed cell penetrating peptide complexes offer highly efficient, low toxicity gene silen
Peptide TAT
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed no
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence
Peptide Concentration Varied via N/P ratio (7–33 screened); optimized ~N/P 25
Rna Concentration 10, 25, or 50 nM (5 h incubation; readout at 48 h)
Mixing Ratio N/P ratio 7, 13, 18, 25, 33 (varied); CaCl2 23.1–69.2 mM added post-complexation
Formulation Format Calcium-condensed CPP/siRNA nanoparticles
Formulation Components TAT + siRNA + CaCl2 (final 23.1–69.2 mM)
Size Nm 60.00
Zeta Mv 15.00
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells A549-luc-C8 (human lung epithelial reporter cell line)
Animal Model
Administration Route
Output Type Luciferase knockdown (% of control; normalized to total protein)
Output Value
Output Units
Output Notes High silencing only when CaCl2 added; best formulations at high CaCl2 (69.2 mM) and moderately high N/P (≈25) achieved ~92% knockdown (≈8.3% luciferase remaining) at 50 nM.
Toxicity Notes No cytotoxicity observed for TAT complexes in A549-luc-C8; free TAT showed negligible cytotoxicity up to 5 mg/mL (MTS assay).
Curation Notes