Discovery and Mechanism of Highly Efficient Cyclic Cell-Penetrating Peptides

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• 作者：Ziqing Qian ; Agnieszka Martyna ; Ryan L. Hard ; Jiang Wang ; George Appiah-Kubi ; Christopher Coss ; Mitch A. Phelps ; Jeremy S. Rossman ; Dehua Pei
• 刊名：Biochemistry
• 出版年：2016
• 出版时间：May 10, 2016
• 年：2016
• 卷：55
• 期：18
• 页码：2601-2612
• 全文大小：586K
• 年卷期：0
• ISSN：1520-4995

文摘

Previous cell-penetrating peptides (CPPs) generally have low cytosolic delivery efficiencies, because of inefficient endosomal escape. In this study, a family of small, amphipathic cyclic peptides was found to be highly efficient CPPs, with cytosolic delivery efficiencies of up to 120% (compared to 2.0% for Tat). These cyclic CPPs bind directly to the plasma membrane phospholipids and enter mammalian cells via endocytosis, followed by efficient release from the endosome. Their total cellular uptake efficiency correlates positively with the binding affinity for the plasma membrane, whereas their endosomal escape efficiency increases with the endosomal membrane-binding affinity. The cyclic CPPs induce membrane curvature on giant unilamellar vesicles and budding of small vesicles, which subsequently collapse into amorphous lipid/peptide aggregates. These data suggest that cyclic CPPs exit the endosome by binding to the endosomal membrane and inducing CPP-enriched lipid domains to bud off as small vesicles. Together with their high proteolytic stability, low cytotoxicity, and oral bioavailability, these cyclic CPPs should provide a powerful system for intracellular delivery of therapeutic agents and chemical probes.