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EXP001951

Paper

A Dual-Ligand Liposomal System Composed of a Cell-Penetrating Peptide and a Mitochondrial RNA Aptamer Synergistically Facilitates Cellular Uptake and Mitochondrial Targeting (2016)

Peptide

R8-modified MITO-Porter (no RNA aptamer)

Sequence: RRRRRRRR

RNA

RNA aptamer (2′-O-methyl, cholesterol-conjugated) [ligand; not therapeutic payload]

All experiment fields

Experiment Id EXP001951
Paper A Dual-Ligand Liposomal System Composed of a Cell-Penetrating Peptide and a Mitochondrial RNA Aptame
Peptide R8-modified MITO-Porter (no RNA aptamer)
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect no
Endosomal Escape Evidence
Peptide Concentration R8 at 10 mol% of total lipids (surface attachment after liposome formation).
Rna Concentration Chol-RNA aptamer at 2.5 mol% of total lipids (dual-ligand variants); NBD-DOPE used as tracer.
Mixing Ratio DOPE/sphingomyelin/NBD-DOPE (9:2:0.1) with ± 2.5 mol% Chol-aptamer; then add stearylated R8 to 10 mol% total lipid.
Formulation Format Liposome (MITO-Porter) with peptide + RNA aptamer dual-ligand surface
Formulation Components DOPE/sphingomyelin/NBD-DOPE (9:2:0.1 molar). R8 device ± Chol-RNA aptamer (RP/MRP/D-arm).
Size Nm 134.00
Zeta Mv 22.00
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells HeLa (human cervix carcinoma) cells
Animal Model
Administration Route
Output Type Uptake + mitochondrial targeting (flow cytometry MFI; confocal colocalization with mitochondria)
Output Value Dual-ligand (aptamer/R8) increases cellular uptake vs R8-only and improves mitochondrial targeting/occupancy; RP/R8 at 2.5 mol% reported as optimal among tested aptamers.
Output Units
Output Notes Readouts: flow cytometry of NBD-labeled liposomes after 3 h; CLSM colocalization with Mitofluor-stained mitochondria; mechanistic inhibitor studies (sucrose/amiloride; FCCP/oligomycin) probe uptake/targeting pathways.
Toxicity Notes
Curation Notes