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Selective Intracellular Delivery of Thiolated Cargo to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as Vectors
[Image: see text] Short histidine-rich peptides could serve as novel activatable vectors for delivering cytotoxic payloads to tumor and neovasculature cells. This explorative study reports preliminary results showing that zinc ions, which are found in elevated levels at neovasculature sites, can tri...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081261/ https://www.ncbi.nlm.nih.gov/pubmed/32201779 http://dx.doi.org/10.1021/acsomega.9b00700 |
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author | Eksteen, J. Johannes Ausbacher, Dominik Vasskog, Terje Rekdal, Øystein Svendsen, John S. M. |
author_facet | Eksteen, J. Johannes Ausbacher, Dominik Vasskog, Terje Rekdal, Øystein Svendsen, John S. M. |
author_sort | Eksteen, J. Johannes |
collection | PubMed |
description | [Image: see text] Short histidine-rich peptides could serve as novel activatable vectors for delivering cytotoxic payloads to tumor and neovasculature cells. This explorative study reports preliminary results showing that zinc ions, which are found in elevated levels at neovasculature sites, can trigger the intracellular delivery of a short antimicrobial peptide when conjugated to a histidine-rich peptide through a disulfide bond. The importance of exofacial thiols in the mode of action of these disulfide-linked conjugates is also shown. |
format | Online Article Text |
id | pubmed-7081261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70812612020-03-20 Selective Intracellular Delivery of Thiolated Cargo to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as Vectors Eksteen, J. Johannes Ausbacher, Dominik Vasskog, Terje Rekdal, Øystein Svendsen, John S. M. ACS Omega [Image: see text] Short histidine-rich peptides could serve as novel activatable vectors for delivering cytotoxic payloads to tumor and neovasculature cells. This explorative study reports preliminary results showing that zinc ions, which are found in elevated levels at neovasculature sites, can trigger the intracellular delivery of a short antimicrobial peptide when conjugated to a histidine-rich peptide through a disulfide bond. The importance of exofacial thiols in the mode of action of these disulfide-linked conjugates is also shown. American Chemical Society 2020-03-06 /pmc/articles/PMC7081261/ /pubmed/32201779 http://dx.doi.org/10.1021/acsomega.9b00700 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Eksteen, J. Johannes Ausbacher, Dominik Vasskog, Terje Rekdal, Øystein Svendsen, John S. M. Selective Intracellular Delivery of Thiolated Cargo to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as Vectors |
title | Selective Intracellular Delivery of Thiolated Cargo
to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as
Vectors |
title_full | Selective Intracellular Delivery of Thiolated Cargo
to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as
Vectors |
title_fullStr | Selective Intracellular Delivery of Thiolated Cargo
to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as
Vectors |
title_full_unstemmed | Selective Intracellular Delivery of Thiolated Cargo
to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as
Vectors |
title_short | Selective Intracellular Delivery of Thiolated Cargo
to Tumor and Neovasculature Cells Using Histidine-Rich Peptides as
Vectors |
title_sort | selective intracellular delivery of thiolated cargo
to tumor and neovasculature cells using histidine-rich peptides as
vectors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081261/ https://www.ncbi.nlm.nih.gov/pubmed/32201779 http://dx.doi.org/10.1021/acsomega.9b00700 |
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