Non-covalent Encapsulation of siRNA with Cell-Penetrating Peptides

Methods Mol Biol. 2021:2282:353-376. doi: 10.1007/978-1-0716-1298-9_19.

Abstract

SiRNAs may act as selective and potent therapeutics, but poor deliverability in vivo is a limitation. Among the recently proposed vectors, cell-penetrating peptides (CPPs), also referred as protein transduction domains (PTDs), allow siRNA stabilization and increased cellular uptake. This chapter aims to guide scientists in the preparation and characterization of CPP-siRNA complexes, particularly the evaluation of novel CPPs variants for siRNA encapsulation and delivery. Herein, we present a collection of methods to determine CPP-siRNA interaction, encapsulation, stability, conformation, transfection, and silencing efficiency.

Keywords: Cell-penetrating peptides; Knockdown; Protein transduction domains; RNA interference; Short interfering RNA; Silencing; Small interfering RNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Cell Line
  • Cell-Penetrating Peptides / chemistry*
  • Cell-Penetrating Peptides / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic
  • Genes, Reporter
  • Humans
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • MCF-7 Cells
  • RNA Interference*
  • RNA, Small Interfering / chemistry
  • RNA, Small Interfering / genetics*
  • RNA, Small Interfering / metabolism
  • Red Fluorescent Protein
  • Research Design
  • Transfection*
  • Workflow

Substances

  • Cell-Penetrating Peptides
  • Luminescent Proteins
  • RNA, Small Interfering