Cationic cell-penetrating peptides as vehicles for siRNA delivery

Author:

Beloor Jagadish1,Zeller Skye1,Choi Chang Seon12,Lee Sang-Kyung2,Kumar Priti1

Affiliation:

1. Section of Infectious Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06510, USA

2. Department of Bioengineering, Institute of Nanoscience & Technology, Hanyang University, Seoul, South Korea

Abstract

RNA interference mediated gene silencing has tremendous applicability in fields ranging from basic biological research to clinical therapy. However, delivery of siRNA across the cell membrane into the cytoplasm, where the RNA silencing machinery is located, is a significant hurdle in most primary cells. Cell-penetrating peptides (CPPs), peptides that possess an intrinsic ability to translocate across cell membranes, have been explored as a means to achieve cellular delivery of siRNA. Approaches using CPPs by themselves or through incorporation into other siRNA delivery platforms have been investigated with the intent of improving cytoplasmic delivery. Here, we review the utilization of CPPs for siRNA delivery with a focus on strategies developed to enhance cellular uptake, endosomal escape and cytoplasmic localization of CPP/siRNA complexes.

Publisher

Future Science Ltd

Subject

Pharmaceutical Science

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