Oligonucleotide delivery with cell surface binding and cell penetrating peptide amphiphile nanospheres

Didem Mumcuoglu, Melis Sardan, Turgay Tekinay, Mustafa O. Guler, Ayse B. Tekinay

Research output: Contribution to journalArticleAcademicpeer-review

25 Citations (Scopus)


A drug delivery system designed specifically for oligonucleotide therapeutics can ameliorate the problems associated with the in vivo delivery of these molecules. The internalization of free oligonucleotides is challenging, and cytotoxicity is the main obstacle for current transfection vehicles. To develop nontoxic delivery vehicles for efficient transfection of oligonucleotides, we designed a self-assembling peptide amphiphile (PA) nanosphere delivery system decorated with cell penetrating peptides (CPPs) containing multiple arginine residues (R4 and R8), and a cell surface binding peptide (KRSR), and report the efficiency of this system in delivering G-3129, a Bcl-2 antisense oligonucleotide (AON). PA/AON (peptide amphiphile/antisense oligonucleotide) complexes were characterized with regards to their size and secondary structure, and their cellular internalization efficiencies were evaluated. The effect of the number of arginine residues on the cellular internalization was investigated by both flow cytometry and confocal imaging, and the results revealed that uptake efficiency improved as the number of arginines in the sequence increased. The combined effect of cell penetration and surface binding property on the cellular internalization and its uptake mechanism was also evaluated by mixing R8-PA and KRSR-PA. R8 and R8/KRSR decorated PAs were found to drastically increase the internalization of AONs compared to nonbioactive PA control. Overall, the KRSR-decorated self-assembled PA nanospheres were demonstrated to be noncytotoxic delivery vectors with high transfection rates and may serve as a promising delivery system for AONs.
Original languageEnglish
Pages (from-to)1584-1591
JournalMolecular Pharmaceutics
Issue number5
Publication statusPublished - May 2015
Externally publishedYes


  • oligonucleotide delivery
  • cell penetrating peptides
  • cellular internalization
  • cell surface proteoglycan binding peptide


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