Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015:1324:223-45.
doi: 10.1007/978-1-4939-2806-4_15.

The Antimicrobial and Antiviral Applications of Cell-Penetrating Peptides

Affiliations
Review

The Antimicrobial and Antiviral Applications of Cell-Penetrating Peptides

Kalle Pärn et al. Methods Mol Biol. 2015.

Abstract

Over the past two decades, cell-penetrating peptides (CPPs) have become increasingly popular both in research and in application. There have been numerous studies on the physiochemical characteristics and behavior of CPPs in various environments; likewise, the mechanisms of entry and delivery capabilities of these peptides have also been extensively researched. Besides the fundamental issues, there is an enormous interest in the delivery capabilities of the peptides as the family of CPPs is a promising and mostly non-toxic delivery vector candidate for numerous medical applications such as gene silencing, transgene delivery, and splice correction. Lately, however, there has been an emerging field of study besides the high-profile gene therapy applications-the use of peptides and CPPs to combat various infections caused by harmful bacteria, fungi, and viruses.In this chapter, we aim to provide a short overview of the history and properties of CPPs which is followed by more thorough descriptions of antimicrobial and antiviral peptides. To achieve this, we analyze the origin of such peptides, give an overview of the mechanisms of action and discuss the various practical applications which are ongoing or have been suggested based on research.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Järver P, Mäger I, Langel Ü. In vivo biodistribution and efficacy of peptide mediated delivery. Trends Pharmacol Sci. 2010;31:528–535. doi: 10.1016/j.tips.2010.07.006. - DOI - PubMed
    1. Lindgren M, Rosenthal-Aizman K, Saar K, et al. Overcoming methotrexate resistance in breast cancer tumour cells by the use of a new cell-penetrating peptide. Biochem Pharmacol. 2006;71:416–425. doi: 10.1016/j.bcp.2005.10.048. - DOI - PubMed
    1. Santra S, Yang H, Stanley JT et al (2005) Rapid and effective labeling of brain tissue using TAT-conjugated CdS:Mn/ZnS quantum dots. Chem Commun (Camb) 3144–3146 - PubMed
    1. Lewin M, Carlesso N, Tung CH, et al. Tat peptide-derivatized magnetic nanoparticles allow in vivo tracking and recovery of progenitor cells. Nat Biotechnol. 2000;18:410–414. doi: 10.1038/74464. - DOI - PubMed
    1. Vasconcelos L, Pärn K, Langel Ü. Therapeutic potential of cell-penetrating peptides. Ther Deliv. 2013;4:573–591. doi: 10.4155/tde.13.22. - DOI - PubMed

Publication types

MeSH terms