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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4931241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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