Cargando…

A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides

Cell penetrating peptides (CPPs) are a promising technology for therapeutic delivery of macromolecular cargos. CPPs have generally used covalent linkages to cargo, ensuring a common fate as one molecule. Conversely, our CPP-adaptor, TAT-CaM, noncovalently binds calmodulin binding sequence (CBS)-cont...

Descripción completa

Detalles Bibliográficos
Autores principales: Morris, Daniel P., Snipes, Lucy C., Hill, Stephanie A., Woods, Michael M., Mbugua, Maria M., Wade, Lydia R., McMurry, Jonathan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720253/
https://www.ncbi.nlm.nih.gov/pubmed/36479201
http://dx.doi.org/10.3389/fphar.2022.1070464
_version_ 1784843515151253504
author Morris, Daniel P.
Snipes, Lucy C.
Hill, Stephanie A.
Woods, Michael M.
Mbugua, Maria M.
Wade, Lydia R.
McMurry, Jonathan L.
author_facet Morris, Daniel P.
Snipes, Lucy C.
Hill, Stephanie A.
Woods, Michael M.
Mbugua, Maria M.
Wade, Lydia R.
McMurry, Jonathan L.
author_sort Morris, Daniel P.
collection PubMed
description Cell penetrating peptides (CPPs) are a promising technology for therapeutic delivery of macromolecular cargos. CPPs have generally used covalent linkages to cargo, ensuring a common fate as one molecule. Conversely, our CPP-adaptor, TAT-CaM, noncovalently binds calmodulin binding sequence (CBS)-containing cargos in calcium rich media then dissociates in the calcium-poor endosomal environment following internalization, enhancing endosomal escape relative to standard CPPs. In this study, we report cell entry of positively charged protein cargos that were not increased by TAT-CaM while cargos based on the negatively charged maltose binding protein (MBP) displayed little intrinsic internalization but were internalized by TAT-CaM. In addition, association of positively charged proteins with negatively charged nucleic acids reduced internalization. This evidence points to the dominant role cargo charge plays in apparent CPP effectiveness. There has been little systematic investigation as to how interaction between CPPs and cargos impacts internalization efficiency. Our adaptors provide a tool that allows combinatorial assays to detect emergent properties. Toward this end we added 4 endolytic peptide (EP) sequences between cargo CBS and MBP moieties to create 4 new cargos and between TAT and CaM to create 4 new adaptors. The new cargos were assayed for internalization alone and with a panel of CPP-adaptors to identify combinations that displayed increased internalization efficiency or other properties. Among the most important results, addition of the EP LAH4 improved adaptor performance and provided some CPP capability to cargos. MBP-LAH4-CBS was internalized more effectively by most adaptors, suggesting this sequence has general stimulatory ability. Two other EPs, Aurein 1.2 and HA2, also provided some CPP capability to their MBP cargos but were unexpectedly antagonistic to internalization by most adaptors due to retention of adaptor/cargo complexes on the cell surface. We thus identified LAH4 as stimulator of internalization in both adaptors and cargos and uncovered new functionality for Aurein 1.2 and HA2, which may be related to their identification as EPs. Future experiments will test new endolytic capabilities made possible with combinatorial approaches.
format Online
Article
Text
id pubmed-9720253
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-97202532022-12-06 A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides Morris, Daniel P. Snipes, Lucy C. Hill, Stephanie A. Woods, Michael M. Mbugua, Maria M. Wade, Lydia R. McMurry, Jonathan L. Front Pharmacol Pharmacology Cell penetrating peptides (CPPs) are a promising technology for therapeutic delivery of macromolecular cargos. CPPs have generally used covalent linkages to cargo, ensuring a common fate as one molecule. Conversely, our CPP-adaptor, TAT-CaM, noncovalently binds calmodulin binding sequence (CBS)-containing cargos in calcium rich media then dissociates in the calcium-poor endosomal environment following internalization, enhancing endosomal escape relative to standard CPPs. In this study, we report cell entry of positively charged protein cargos that were not increased by TAT-CaM while cargos based on the negatively charged maltose binding protein (MBP) displayed little intrinsic internalization but were internalized by TAT-CaM. In addition, association of positively charged proteins with negatively charged nucleic acids reduced internalization. This evidence points to the dominant role cargo charge plays in apparent CPP effectiveness. There has been little systematic investigation as to how interaction between CPPs and cargos impacts internalization efficiency. Our adaptors provide a tool that allows combinatorial assays to detect emergent properties. Toward this end we added 4 endolytic peptide (EP) sequences between cargo CBS and MBP moieties to create 4 new cargos and between TAT and CaM to create 4 new adaptors. The new cargos were assayed for internalization alone and with a panel of CPP-adaptors to identify combinations that displayed increased internalization efficiency or other properties. Among the most important results, addition of the EP LAH4 improved adaptor performance and provided some CPP capability to cargos. MBP-LAH4-CBS was internalized more effectively by most adaptors, suggesting this sequence has general stimulatory ability. Two other EPs, Aurein 1.2 and HA2, also provided some CPP capability to their MBP cargos but were unexpectedly antagonistic to internalization by most adaptors due to retention of adaptor/cargo complexes on the cell surface. We thus identified LAH4 as stimulator of internalization in both adaptors and cargos and uncovered new functionality for Aurein 1.2 and HA2, which may be related to their identification as EPs. Future experiments will test new endolytic capabilities made possible with combinatorial approaches. Frontiers Media S.A. 2022-11-21 /pmc/articles/PMC9720253/ /pubmed/36479201 http://dx.doi.org/10.3389/fphar.2022.1070464 Text en Copyright © 2022 Morris, Snipes, Hill, Woods, Mbugua, Wade and McMurry. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Morris, Daniel P.
Snipes, Lucy C.
Hill, Stephanie A.
Woods, Michael M.
Mbugua, Maria M.
Wade, Lydia R.
McMurry, Jonathan L.
A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides
title A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides
title_full A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides
title_fullStr A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides
title_full_unstemmed A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides
title_short A reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides
title_sort reversible cell penetrating peptide-cargo linkage allows dissection of cell penetrating peptide- and cargo-dependent effects on internalization and identifies new functionalities of putative endolytic peptides
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720253/
https://www.ncbi.nlm.nih.gov/pubmed/36479201
http://dx.doi.org/10.3389/fphar.2022.1070464
work_keys_str_mv AT morrisdanielp areversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT snipeslucyc areversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT hillstephaniea areversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT woodsmichaelm areversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT mbuguamariam areversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT wadelydiar areversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT mcmurryjonathanl areversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT morrisdanielp reversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT snipeslucyc reversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT hillstephaniea reversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT woodsmichaelm reversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT mbuguamariam reversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT wadelydiar reversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides
AT mcmurryjonathanl reversiblecellpenetratingpeptidecargolinkageallowsdissectionofcellpenetratingpeptideandcargodependenteffectsoninternalizationandidentifiesnewfunctionalitiesofputativeendolyticpeptides