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EXP001978

Paper

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

Peptide

Ab-CPP-MSP-siRNA (cetuximab–PEG–LMWP–GGPLGVR–siRNA; ARC)

Sequence: VSRRRRGGRRRRRRGGPLGVR

RNA

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

All experiment fields

Experiment Id EXP001978
Paper Antibody-siRNA conjugates (ARCs) using multifunctional peptide as a tumor enzyme cleavable linker me
Peptide Ab-CPP-MSP-siRNA (cetuximab–PEG–LMWP–GGPLGVR–siRNA; ARC)
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.
Formulation Format Antibody–multifunctional peptide–siRNA covalent conjugate (ARC)
Formulation Components Cetuximab linked to PEG–LMWP–GGPLGVR–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/activation (confocal; Ab/siRNA separation after substrate cleavage)
Output Value Strong intracellular siRNA signal in HCT116 and HT1080; weak in SW620 (controls).
Output Units
Output Notes Activation depends on MMP-2 cleavage; no separate functional knockdown reported specifically for MSP construct in main text.
Toxicity Notes
Curation Notes