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EXP001682

Paper

Efficient splicing correction by PNA conjugation to an R6-Penetratin delivery peptide (2007)

Peptide

(R-Ahx-R)4–PNA705 (stable)

Sequence: R-Ahx-RR-Ahx-RR-Ahx-RR-Ahx-R-C

RNA

PNA (antisense steric-block)

All experiment fields

Experiment Id EXP001682
Paper Efficient splicing correction by PNA conjugation to an R6-Penetratin delivery peptide
Peptide (R-Ahx-R)4–PNA705 (stable)
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed no
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence
Peptide Concentration 0.1–2.5 µM conjugate tested (typically 1 µM; 4 h incubation in OptiMEM)
Rna Concentration Same as conjugate (PNA is covalently linked); 0.1–2.5 µM
Mixing Ratio Covalent conjugate (1:1 peptide:PNA)
Formulation Format CPP–PNA conjugate (thioacetyl stable linker or disulfide linker)
Formulation Components CPP peptide covalently conjugated to PNA705 (or scrambled) (± chloroquine 100 µM in some conditions)
Size Nm
Zeta Mv
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells HeLa pLuc705 splice-correction reporter cells
Animal Model
Administration Route
Output Type splice correction (luciferase)
Output Value Moderate luciferase up-regulation at 1 µM (less than R6Pen).
Output Units
Output Notes Second-best among tested CPPs in Figure 1 comparison at 1 µM without endosomolytic agent.
Toxicity Notes
Curation Notes