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EXP001186

Paper

Design and evaluation of a stearylated multicomponent peptide-siRNA nanocomplex for efficient cellular siRNA delivery (2017)

Peptide

DEN-K(GALA)-TAT-K(STR)

Sequence: Multicomponent peptide (poly-L-lysine dendron + GALA + TAT) with stearic acid (STR) on C-terminal Lys side chain

RNA

siRNA

All experiment fields

Experiment Id EXP001186
Paper Design and evaluation of a stearylated multicomponent peptide-siRNA nanocomplex for efficient cellul
Peptide DEN-K(GALA)-TAT-K(STR)
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence yes
Peptide Concentration Peptide/siRNA molar ratios tested 25–125 (uptake/knockdown); 50–200 for DLS; complexes formed in 20 mM HEPES pH 7.2, 30 min RT
Rna Concentration 20 nM siRNA (uptake/knockdown assays); 10 nM Alexa488-siRNA for confocal trafficking; 100 ng siRNA for gel shift
Mixing Ratio Peptide:siRNA molar ratio (optimal ~100 for compact particles and knockdown)
Formulation Format Electrostatic peptide/siRNA nanocomplex (nanoparticle)
Formulation Components DEN-K(GALA)-TAT-K(STR) + eGFP siRNA in 20 mM HEPES buffer pH 7.2 (30 min incubation)
Size Nm 92.50
Zeta Mv 44.20
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells Stable eGFP-expressing HeLa cells
Animal Model
Administration Route
Output Type In vitro functional RNA effect (eGFP knockdown at protein and mRNA levels)
Output Value ~58% reduction in eGFP protein at molar ratio 100 (48 h); ~57% decrease in eGFP mRNA (qRT-PCR)
Output Units
Output Notes Enhanced uptake vs non-lipidic analog; compact ~100 nm positively charged particles; best knockdown at molar ratio 100 with no further improvement at 125.
Toxicity Notes Low cytotoxicity under assay conditions (∼15% viability loss at 2 µM vector with 20 nM siRNA); less toxic than 25 kDa bPEI control.
Curation Notes