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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...

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Autores principales: McCandless, Kayla, Mishra, Sanjay, Stiltner, Jeffrey, Feldman, Kyle S., Yagi, Hisato, Yurko, Raymond, Islam, Kazi, Brown, Jonathan M., Frizzell, Raymond, Zahid, Maliha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2021
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.
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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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