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. 2017 Jun 30;12(6):e0180578. doi: 10.1371/journal.pone.0180578

Fig 1. Diagrams of various peptides used in the study and the putative structure of complexes formed between the peptides and siRNA.

Fig 1

In Fig 1A, the domain structure of the peptides is shown. The siRNA binding peptides have a myristoylated amino-terminus, followed by an arginine-rich region (R9), and a cell targeting motif (LyP-1 or iRGD). The endosomal release peptide possesses an endosomal release motif flanked by a glutamic acid-rich region. In Fig 1B, the formation of nanoparticles by the siRNA-binding peptide is shown, and the incorporation of siRNA and the endosomal release peptide into the particles after their addition.