Influence of Aza-Glycine Substitution on the Internalization of Penetratin

• Main Authors: Karima Tarchoun (Author), Dóra Soltész (Author), Viktor Farkas (Author), Ho-Jin Lee (Author), Ildikó Szabó (Author), Zoltán Bánóczi (Author)
• Format: Book
• Published: MDPI AG, 2024-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 10.3390/pharmaceutics16040477; 1999-4923
• Keywords: cell-penetrating peptides; penetratin; aza-amino acid; aza-peptide; flow cytometry; Pharmacy and materia medica; RS1-441
• Source: Pharmaceutics, Vol 16, Iss 4, p 477 (2024)

The cell-penetrating peptide (CPP) penetratin has gained much attention over many years due to its potential role as a transporter for a broad range of cargo into cells. The modification of penetratin has been extensively investigated too. Aza-peptides are peptide analogs in which one or more of the amino residues are replaced by a semicarbazide. This substitution results in conformational restrictions and modifications in hydrogen bonding properties, which affect the structure and may lead to enhanced activity and selectivity of the modified peptide. In this work, the Trp residues of penetratin were substituted by aza-glycine or glycine residues to examine the effect of these modifications on the cellular uptake and the internalization mechanism. The substitution of Trp⁴⁸ or Trp^48,56 dramatically reduced the internalization, showing the importance of Trp⁴⁸ in cellular uptake. Interestingly, while aza-glycine in the position of Trp⁵⁶ increased the cellular uptake, Gly reduced it. The two Trp-modified derivatives showed altered internalization pathways, too. Based on our knowledge, this is the first study about the effect of aza-amino acid substitution on the cell entry of CPPs. Our results suggest that aza-amino acid insertion is a useful modification to change the internalization of a CPP.