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Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics
Cell penetrating peptides are unique, 5–30 amino acid long peptides that are able to breach cell membrane barriers and carry cargoes intracellularly in a functional form. Our prior work identified a synthetic, non-naturally occurring 12-amino acid long peptide that we termed cardiac targeting peptid...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609903/ https://www.ncbi.nlm.nih.gov/pubmed/34816257 http://dx.doi.org/10.21203/rs.3.rs-1056707/v1 |
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author | McCandless, Kayla Mishra, Sanjay Stiltner, Jeffrey Feldman, Kyle S. Yagi, Hisato Yurko, Raymond Islam, Kazi Brown, Jonathan M. Frizzell, Raymond Zahid, Maliha |
author_facet | McCandless, Kayla Mishra, Sanjay Stiltner, Jeffrey Feldman, Kyle S. Yagi, Hisato Yurko, Raymond Islam, Kazi Brown, Jonathan M. Frizzell, Raymond Zahid, Maliha |
author_sort | McCandless, Kayla |
collection | PubMed |
description | Cell penetrating peptides are unique, 5–30 amino acid long peptides that are able to breach cell membrane barriers and carry cargoes intracellularly in a functional form. Our prior work identified a synthetic, non-naturally occurring 12-amino acid long peptide that we termed cardiac targeting peptide (CTP: APWHLSSQYSRT) due to its ability to transduce cardiomyocytes in vivo. Studies looking into its mechanism of transduction identified two lung targeting peptides (LTPs), S7A (APWHLSAQYSRT) and R11A (APWHLSSQYSAT). These peptides robustly transduced human bronchial epithelial cell lines in vitro and mouse lung tissue in vivo. This uptake occurred independently of clathrin mediated endocytosis. Biodistribution studies of R11A showed peak uptake at 15 minutes with uptake in liver but not kidneys, indicating primarily a hepatobiliary mode of excretion. Cyclic version of both peptides was ~100-fold more efficient in permeating cells than their linear counterparts. As proof of principle, we conjugated anti-spike and anti-envelope SARS-CoV-2 siRNAs to cyclized R11A and demonstrate anti-viral efficacy in vitro. Our work presented here identifies two novel lung-specific cell penetrating peptides that could potentially deliver myriad therapeutic cargoes to lung tissue. |
format | Online Article Text |
id | pubmed-8609903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-86099032021-11-24 Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics McCandless, Kayla Mishra, Sanjay Stiltner, Jeffrey Feldman, Kyle S. Yagi, Hisato Yurko, Raymond Islam, Kazi Brown, Jonathan M. Frizzell, Raymond Zahid, Maliha Res Sq Article Cell penetrating peptides are unique, 5–30 amino acid long peptides that are able to breach cell membrane barriers and carry cargoes intracellularly in a functional form. Our prior work identified a synthetic, non-naturally occurring 12-amino acid long peptide that we termed cardiac targeting peptide (CTP: APWHLSSQYSRT) due to its ability to transduce cardiomyocytes in vivo. Studies looking into its mechanism of transduction identified two lung targeting peptides (LTPs), S7A (APWHLSAQYSRT) and R11A (APWHLSSQYSAT). These peptides robustly transduced human bronchial epithelial cell lines in vitro and mouse lung tissue in vivo. This uptake occurred independently of clathrin mediated endocytosis. Biodistribution studies of R11A showed peak uptake at 15 minutes with uptake in liver but not kidneys, indicating primarily a hepatobiliary mode of excretion. Cyclic version of both peptides was ~100-fold more efficient in permeating cells than their linear counterparts. As proof of principle, we conjugated anti-spike and anti-envelope SARS-CoV-2 siRNAs to cyclized R11A and demonstrate anti-viral efficacy in vitro. Our work presented here identifies two novel lung-specific cell penetrating peptides that could potentially deliver myriad therapeutic cargoes to lung tissue. American Journal Experts 2021-11-15 /pmc/articles/PMC8609903/ /pubmed/34816257 http://dx.doi.org/10.21203/rs.3.rs-1056707/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article McCandless, Kayla Mishra, Sanjay Stiltner, Jeffrey Feldman, Kyle S. Yagi, Hisato Yurko, Raymond Islam, Kazi Brown, Jonathan M. Frizzell, Raymond Zahid, Maliha Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics |
title | Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics |
title_full | Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics |
title_fullStr | Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics |
title_full_unstemmed | Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics |
title_short | Novel Lung Targeting Cell Penetrating Peptides as Vectors for Delivery of Therapeutics |
title_sort | novel lung targeting cell penetrating peptides as vectors for delivery of therapeutics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609903/ https://www.ncbi.nlm.nih.gov/pubmed/34816257 http://dx.doi.org/10.21203/rs.3.rs-1056707/v1 |
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