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EXP001979

Paper

Antibody-siRNA conjugates (ARCs) using multifunctional peptide as a tumor enzyme cleavable linker mediated effective intracellular delivery of siRNA (2021)

Peptide

Ab-CPP-siRNA (cetuximab–PEG–LMWP–siRNA; no substrate control)

Sequence: VSRRRRGGRRRRRR

RNA

siRNA (anti-EGFP; thiol-modified; Cy3/TAMRA labeled variants used for imaging)

All experiment fields

Experiment Id EXP001979
Paper Antibody-siRNA conjugates (ARCs) using multifunctional peptide as a tumor enzyme cleavable linker me
Peptide Ab-CPP-siRNA (cetuximab–PEG–LMWP–siRNA; no substrate control)
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect no
Endosomal Escape Evidence
Peptide Concentration
Rna Concentration Not consistently stated for uptake; silencing assays used 100 nM.
Mixing Ratio Covalent ARC control.
Formulation Format Antibody–CPP–siRNA covalent conjugate (no substrate)
Formulation Components Cetuximab linked to PEG–LMWP–siRNA.
Size Nm
Zeta Mv
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells Uptake studies: HCT116 (EGFR+), HT1080 (EGFR+), SW620 (EGFR low) with confocal microscopy
Animal Model
Administration Route
Output Type In vitro uptake/colocalization control (confocal)
Output Value Lower intracellular signal; Ab and siRNA signals largely colocalized (CPP remains masked).
Output Units
Output Notes Used to demonstrate importance of substrate peptide for release/activation.
Toxicity Notes
Curation Notes