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EXP000831

Paper

N-terminal modification of an LAH4-derived peptide increases mRNA delivery in the presence of serum (2024)

Peptide

LAH4-A1-Trp2

Sequence: WWKKALLAHALHLLAALALHLAHLLKKA

RNA

mRNA

All experiment fields

Experiment Id EXP000831
Paper N-terminal modification of an LAH4-derived peptide increases mRNA delivery in the presence of serum
Peptide LAH4-A1-Trp2
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed no
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence
Peptide Concentration
Rna Concentration
Mixing Ratio Typically 5 µg peptide per 0.5 µg mRNA (HCT116) or 7 µg peptide per 1 µg mRNA (HEK293T GFP/Cy5 experiments); conditions varied.
Formulation Format peptide/mRNA complexes (polyplex)
Formulation Components Buffers used for complexation included 10 mM acetate pH5, 150 mM NaCl, or 10 mM phosphate buffer pH6.25 (also PBS, HBG in optimization).
Size Nm 590.00
Zeta Mv
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells HCT116
Animal Model
Administration Route
Output Type Functional reporter expression (luciferase and/or GFP)
Output Value
Output Units
Output Notes Modified LAH4-A1 peptides evaluated mainly in HCT116/HEK293T (luciferase/GFP); Tyr2 and Sali show improved activity in phosphate pH6.25 and improved serum tolerance. DLS in 10 mM phosphate pH6.25: 590 nm ±208 (PDI 0.299) with 10 µg peptide +0.8 µg FLuc mRNA.
Toxicity Notes
Curation Notes