Back to browse

EXP001458

Paper

Cyclic peptide-based nanostructures as efficient siRNA carriers (2018)

Peptide

CP II

Sequence: Cyclo[WWWGGRRRGG]

RNA

siRNA

All experiment fields

Experiment Id EXP001458
Paper Cyclic peptide-based nanostructures as efficient siRNA carriers
Peptide CP II
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed no
Label Confidence medium
In Vitro Functional Effect no
Endosomal Escape Evidence
Peptide Concentration Uptake: 30 µM (FACS) or ~8 µM (confocal). Knockdown: 24 µM.
Rna Concentration Uptake: 200 nM (FACS) or ~80 nM (confocal). Knockdown: 600 nM.
Mixing Ratio Confocal: 0.04 nmol FAM-siRNA + 4 nmol peptide in 500 µL DMEM, 30 min complexation. FACS: 200 nM FAM-siRNA + 30 µM peptide in Opti-MEM, 30 min. Western blot: 24 µM peptide + 600 nM GAPDH siRNA in 500 µL serum-free DMEM, 30 min; incubate cells 3 h then add complete media and culture 48 h.
Formulation Format Self-assembled cyclic peptide nanostructures / peptide–siRNA nanocomplexes (noncovalent)
Formulation Components CP II + GAPDH siRNA (FAM-labeled for uptake; unlabeled for knockdown)
Size Nm 72.71
Zeta Mv
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells HCT116 human colon cancer cells
Animal Model
Administration Route
Output Type Uptake (confocal microscopy + flow cytometry) and functional gene silencing (GAPDH protein by Western blot)
Output Value
Output Units
Output Notes Did not significantly influence FAM-siRNA uptake (reported as not significant; data not shown). Included in gene-silencing evaluation, but no explicit knockdown result reported.
Toxicity Notes Cyclic peptides showed >90% viability at 10 µM (24 h). siRNA/peptide complexes showed no significant cytotoxicity except CP I showed some cytotoxicity relative to other complexes; lipofectamine 2000 showed significant cytotoxicity.
Curation Notes