4.5 Article

A self-assembling peptidic platform to boost the cellular uptake and nuclear delivery of oligonucleotides

Journal

BIOMATERIALS SCIENCE
Volume 10, Issue 15, Pages 4309-4323

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2bm00826b

Keywords

-

Funding

  1. Swiss Nanoscience Institute (SNI)
  2. National Centre of Competence in Research-Molecular Systems Engineering (NCCR-MSE)
  3. University of Basel
  4. ETH Zurich

Ask authors/readers for more resources

The design of non-viral vectors that efficiently deliver genetic materials into cells, particularly to the nucleus, is still a major challenge. This study introduces a delivery platform based on self-assembled peptides, which can form micellar nanostructures with nuclear localization signal (NLS). These nanostructures can encapsulate various oligonucleotides and enhance cellular uptake and nuclear translocation. The platform shows potential for efficiently delivering genetic payloads and has implications in basic research and biomedicine.
The design of non-viral vectors that efficiently deliver genetic materials into cells, in particular to the nucleus, remains a major challenge in gene therapy and vaccine development. To tackle the problems associated with cellular uptake and nuclear targeting, here we introduce a delivery platform based on the self-assembly of an amphiphilic peptide carrying an N-terminal KRKR sequence that functions as a nuclear localization signal (NLS). By means of a single-step self-assembly process, the amphiphilic peptides afford the generation of NLS-functionalized multicompartment micellar nanostructures that can embed various oligonucleotides between their individual compartments. Detailed physicochemical, cellular and ultrastructural analyses demonstrated that integrating an NLS in the hydrophilic domain of the peptide along with tuning its hydrophobic domain led to self-assembled DNA-loaded multicompartment micelles (MCMs) with enhanced cellular uptake and nuclear translocation. We showed that the nuclear targeting ensued via the NLS interaction with the nuclear transport receptors of the karyopherin family. Importantly, we observed that the treatment of MCF-7 cells with NLS-MCMs loaded with anti-BCL2 antisense oligonucleotides resulted in up to 86% knockdown of BCL2, an inhibitor of apoptosis that is overexpressed in more than half of all human cancers. We envision that this platform can be used to efficiently entrap and deliver diverse genetic payloads to the nucleus and find applications in basic research and biomedicine.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available