Sequence: AGYLLGKINLKALAALAKKIL
| Experiment Id | EXP001467 |
|---|---|
| Paper | Cell-Penetrating Peptide and siRNA-Mediated Therapeutic Effects on Endometriosis and Cancer In Vitro |
| Peptide | PepFect6 (PF6) |
| Delivery Success Class | no |
| In Vivo Flag | no |
| Uptake Confirmed | no |
| Label Confidence | high |
| In Vitro Functional Effect | yes |
| Endosomal Escape Evidence | |
| Peptide Concentration | Set by molar ratio 40 (CPP:siRNA). Exact µM peptide depends on siRNA concentration. |
| Rna Concentration | 2D monolayer: 100 nM siRNA final in medium |
| Mixing Ratio | CPP/siRNA NPs formed at molar ratio 40 (CPP:siRNA) by mixing peptide + siRNA in MilliQ water (pH 5.3–6.3) and incubating 45 min at room temperature before transfection. |
| Formulation Format | CPP/siRNA nanoparticles (noncovalent electrostatic NPs) |
| Formulation Components | PepFect6 (PF6) + siRRM2 |
| Size Nm | |
| Zeta Mv | |
| Model Scope | in_vitro |
| Model Type | in vitro |
| Cell Lines Or Primary Cells | U-87MG human glioblastoma cells (2D monolayer) |
| Animal Model | |
| Administration Route | |
| Output Type | Functional RNA effect: RRM2 mRNA knockdown (qRT-PCR, 48 h), RRM2 protein decrease (ICC), cell-cycle arrest (PI-FACS), reduced invasion (Matrigel). |
| Output Value | |
| Output Units | |
| Output Notes | Significant RRM2 knockdown vs pure siRRM2; RRM2 protein decreased by immunocytochemistry; G1/S cell-cycle arrest and strong reduction of invasiveness reported. Reported (from prior characterizations): ~30–40 nm (TEM) and ~100–200 nm (DLS) when complexed with siRNA (not newly measured in this paper). |
| Toxicity Notes | Authors reference prior cytotoxicity characterization for PF6/NF70 at similar conditions; current work focuses on knockdown and phenotypic assays (migration/invasion/proliferation). |
| Curation Notes |