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A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries

Traumatic brain injury (TBI) is a major health and socio-economic problem, but no pharmacological agent is currently approved for the treatment of acute TBI. Thus, there is a great need for advances in this field. Here, we describe a short peptide (sequence CAQK) identified by in vivo phage display...

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Autores principales: Mann, Aman P., Scodeller, Pablo, Hussain, Sazid, Joo, Jinmyoung, Kwon, Ester, Braun, Gary B., Mölder, Tarmo, She, Zhi-Gang, Kotamraju, Venkata Ramana, Ranscht, Barbara, Krajewski, Stan, Teesalu, Tambet, Bhatia, Sangeeta, Sailor, Michael J., Ruoslahti, Erkki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931241/
https://www.ncbi.nlm.nih.gov/pubmed/27351915
http://dx.doi.org/10.1038/ncomms11980
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author Mann, Aman P.
Scodeller, Pablo
Hussain, Sazid
Joo, Jinmyoung
Kwon, Ester
Braun, Gary B.
Mölder, Tarmo
She, Zhi-Gang
Kotamraju, Venkata Ramana
Ranscht, Barbara
Krajewski, Stan
Teesalu, Tambet
Bhatia, Sangeeta
Sailor, Michael J.
Ruoslahti, Erkki
author_facet Mann, Aman P.
Scodeller, Pablo
Hussain, Sazid
Joo, Jinmyoung
Kwon, Ester
Braun, Gary B.
Mölder, Tarmo
She, Zhi-Gang
Kotamraju, Venkata Ramana
Ranscht, Barbara
Krajewski, Stan
Teesalu, Tambet
Bhatia, Sangeeta
Sailor, Michael J.
Ruoslahti, Erkki
author_sort Mann, Aman P.
collection PubMed
description Traumatic brain injury (TBI) is a major health and socio-economic problem, but no pharmacological agent is currently approved for the treatment of acute TBI. Thus, there is a great need for advances in this field. Here, we describe a short peptide (sequence CAQK) identified by in vivo phage display screening in mice with acute brain injury. The CAQK peptide selectively binds to injured mouse and human brain, and systemically injected CAQK specifically homes to sites of brain injury in mouse models. The CAQK target is a proteoglycan complex upregulated in brain injuries. Coupling to CAQK increased injury site accumulation of systemically administered molecules ranging from a drug-sized molecule to nanoparticles. CAQK-coated nanoparticles containing silencing oligonucleotides provided the first evidence of gene silencing in injured brain parenchyma by systemically administered siRNA. These findings present an effective targeting strategy for the delivery of therapeutics in clinical management of acute brain injuries.
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spelling pubmed-49312412016-07-12 A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries Mann, Aman P. Scodeller, Pablo Hussain, Sazid Joo, Jinmyoung Kwon, Ester Braun, Gary B. Mölder, Tarmo She, Zhi-Gang Kotamraju, Venkata Ramana Ranscht, Barbara Krajewski, Stan Teesalu, Tambet Bhatia, Sangeeta Sailor, Michael J. Ruoslahti, Erkki Nat Commun Article Traumatic brain injury (TBI) is a major health and socio-economic problem, but no pharmacological agent is currently approved for the treatment of acute TBI. Thus, there is a great need for advances in this field. Here, we describe a short peptide (sequence CAQK) identified by in vivo phage display screening in mice with acute brain injury. The CAQK peptide selectively binds to injured mouse and human brain, and systemically injected CAQK specifically homes to sites of brain injury in mouse models. The CAQK target is a proteoglycan complex upregulated in brain injuries. Coupling to CAQK increased injury site accumulation of systemically administered molecules ranging from a drug-sized molecule to nanoparticles. CAQK-coated nanoparticles containing silencing oligonucleotides provided the first evidence of gene silencing in injured brain parenchyma by systemically administered siRNA. These findings present an effective targeting strategy for the delivery of therapeutics in clinical management of acute brain injuries. Nature Publishing Group 2016-06-28 /pmc/articles/PMC4931241/ /pubmed/27351915 http://dx.doi.org/10.1038/ncomms11980 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Mann, Aman P.
Scodeller, Pablo
Hussain, Sazid
Joo, Jinmyoung
Kwon, Ester
Braun, Gary B.
Mölder, Tarmo
She, Zhi-Gang
Kotamraju, Venkata Ramana
Ranscht, Barbara
Krajewski, Stan
Teesalu, Tambet
Bhatia, Sangeeta
Sailor, Michael J.
Ruoslahti, Erkki
A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries
title A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries
title_full A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries
title_fullStr A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries
title_full_unstemmed A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries
title_short A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries
title_sort peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931241/
https://www.ncbi.nlm.nih.gov/pubmed/27351915
http://dx.doi.org/10.1038/ncomms11980
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