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Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs

Here we describe an entirely new class of cell-penetrating peptide (CPP) represented by the short peptide Xentry (LCLRPVG) derived from an N-terminal region of the X-protein of the hepatitis B virus. Xentry permeates adherent cells using syndecan-4 as a portal for entry, and is uniquely restricted f...

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Autores principales: Montrose, Kristopher, Yang, Yi, Sun, Xueying, Wiles, Siouxsie, Krissansen, Geoffrey W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627194/
https://www.ncbi.nlm.nih.gov/pubmed/23588666
http://dx.doi.org/10.1038/srep01661
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author Montrose, Kristopher
Yang, Yi
Sun, Xueying
Wiles, Siouxsie
Krissansen, Geoffrey W.
author_facet Montrose, Kristopher
Yang, Yi
Sun, Xueying
Wiles, Siouxsie
Krissansen, Geoffrey W.
author_sort Montrose, Kristopher
collection PubMed
description Here we describe an entirely new class of cell-penetrating peptide (CPP) represented by the short peptide Xentry (LCLRPVG) derived from an N-terminal region of the X-protein of the hepatitis B virus. Xentry permeates adherent cells using syndecan-4 as a portal for entry, and is uniquely restricted from entering syndecan-deficient, non-adherent cells, such as resting blood cells. Intravenous injection of Xentry alone or conjugated to β-galactosidase led to its delivery to most tissues in mice, except circulating blood cells. There was a predilection for uptake by epithelia. Anti-B-raf antibodies and siRNAs linked to Xentry were capable of killing B-raf-dependent melanoma cells. Xentry represents a new class of CPP with properties that are potentially advantageous for life science and therapeutic applications.
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spelling pubmed-36271942013-04-16 Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs Montrose, Kristopher Yang, Yi Sun, Xueying Wiles, Siouxsie Krissansen, Geoffrey W. Sci Rep Article Here we describe an entirely new class of cell-penetrating peptide (CPP) represented by the short peptide Xentry (LCLRPVG) derived from an N-terminal region of the X-protein of the hepatitis B virus. Xentry permeates adherent cells using syndecan-4 as a portal for entry, and is uniquely restricted from entering syndecan-deficient, non-adherent cells, such as resting blood cells. Intravenous injection of Xentry alone or conjugated to β-galactosidase led to its delivery to most tissues in mice, except circulating blood cells. There was a predilection for uptake by epithelia. Anti-B-raf antibodies and siRNAs linked to Xentry were capable of killing B-raf-dependent melanoma cells. Xentry represents a new class of CPP with properties that are potentially advantageous for life science and therapeutic applications. Nature Publishing Group 2013-04-16 /pmc/articles/PMC3627194/ /pubmed/23588666 http://dx.doi.org/10.1038/srep01661 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Article
Montrose, Kristopher
Yang, Yi
Sun, Xueying
Wiles, Siouxsie
Krissansen, Geoffrey W.
Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs
title Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs
title_full Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs
title_fullStr Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs
title_full_unstemmed Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs
title_short Xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs
title_sort xentry, a new class of cell-penetrating peptide uniquely equipped for delivery of drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627194/
https://www.ncbi.nlm.nih.gov/pubmed/23588666
http://dx.doi.org/10.1038/srep01661
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