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EXP001826

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

All experiment fields

Experiment Id EXP001826
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
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