Conjugate for efficient delivery of short interfering RNA (siRNA) into mammalian cells

FEBS Lett. 2004 Jan 30;558(1-3):63-8. doi: 10.1016/S0014-5793(03)01505-9.

Abstract

The efficient delivery of short interfering RNAs (siRNAs) into cells provides a powerful approach to study cellular functions. SiRNAs were coupled to the membrane permeant peptides (MPPs) penetratin and transportan to improve their uptake by cells. Thiol-containing siRNAs corresponding to luciferase, or green fluorescent protein (GFP) transgenes, were synthesized and conjugated to penetratin or transportan via a disulfide bond that is labile in the reducing environment of the cytoplasm. These MPP-siRNAs efficiently reduced transient and stable expression of reporter transgenes in several mammalian cell types in a high proportion of cells, and demonstrated equivalent or better delivery characteristics than cationic liposomes with fewer manipulations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • COS Cells
  • Carrier Proteins / metabolism
  • Cell Membrane / metabolism
  • Cell-Penetrating Peptides
  • Chlorocebus aethiops
  • Cricetinae
  • Cricetulus
  • Cytoplasm / metabolism
  • Disulfides / metabolism
  • Fibroblasts / metabolism
  • Galanin
  • Gene Silencing
  • Gene Transfer Techniques*
  • Genes, Reporter
  • Green Fluorescent Proteins
  • Luciferases / metabolism
  • Luminescent Proteins / metabolism
  • Mice
  • Peptide Fragments / metabolism
  • RNA, Small Interfering / genetics*
  • RNA, Small Interfering / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Transgenes
  • Wasp Venoms

Substances

  • Carrier Proteins
  • Cell-Penetrating Peptides
  • Disulfides
  • Luminescent Proteins
  • Peptide Fragments
  • RNA, Small Interfering
  • Recombinant Fusion Proteins
  • Wasp Venoms
  • transportan
  • Green Fluorescent Proteins
  • Galanin
  • penetratin
  • Luciferases