A real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.

Cell-penetrating peptides (CPPs) are capable of transporting molecules to which they are tethered across cellular membranes. Unsurprisingly, CPPs have attracted attention for their potential drug delivery applications, but several technical hurdles remain to be overcome. Chief among them is the so-c...

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Autores principales: Schuyler B Gentry, Scott J Nowak, Xuelei Ni, Stephanie A Hill, Lydia R Wade, William R Clark, Aidan P Keelaghan, Daniel P Morris, Jonathan L McMurry
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:9451a358a4f44d599a4c82ed713d4cea2021-12-02T20:04:44ZA real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.1932-620310.1371/journal.pone.0254468https://doaj.org/article/9451a358a4f44d599a4c82ed713d4cea2021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0254468https://doaj.org/toc/1932-6203Cell-penetrating peptides (CPPs) are capable of transporting molecules to which they are tethered across cellular membranes. Unsurprisingly, CPPs have attracted attention for their potential drug delivery applications, but several technical hurdles remain to be overcome. Chief among them is the so-called 'endosomal escape problem,' i.e. the propensity of CPP-cargo molecules to be endocytosed but remain entrapped in endosomes rather than reaching the cytosol. Previously, a CPP fused to calmodulin that bound calmodulin binding site-containing cargos was shown to efficiently deliver cargos to the cytoplasm, effectively overcoming the endosomal escape problem. The CPP-adaptor, "TAT-CaM," evinces delivery at nM concentrations and more rapidly than we had previously been able to measure. To better understand the kinetics and mechanism of CPP-adaptor-mediated cargo delivery, a real-time cell penetrating assay was developed in which a flow chamber containing cultured cells was installed on the stage of a confocal microscope to allow for observation ab initio. Also examined in this study was an improved CPP-adaptor that utilizes naked mole rat (Heterocephalus glaber) calmodulin in place of human and results in superior internalization, likely due to its lesser net negative charge. Adaptor-cargo complexes were delivered into the flow chamber and fluorescence intensity in the midpoint of baby hamster kidney cells was measured as a function of time. Delivery of 400 nM cargo was observed within seven minutes and fluorescence continued to increase linearly as a function of time. Cargo-only control experiments showed that the minimal uptake which occurred independently of the CPP-adaptor resulted in punctate localization consistent with endosomal entrapment. A distance analysis was performed for cell-penetration experiments in which CPP-adaptor-delivered cargo showing wider dispersions throughout cells as compared to an analogous covalently-bound CPP-cargo. Small molecule endocytosis inhibitors did not have significant effects upon delivery. The real-time assay is an improvement upon static endpoint assays and should be informative in a broad array of applications.Schuyler B GentryScott J NowakXuelei NiStephanie A HillLydia R WadeWilliam R ClarkAidan P KeelaghanDaniel P MorrisJonathan L McMurryPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 9, p e0254468 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Schuyler B Gentry
Scott J Nowak
Xuelei Ni
Stephanie A Hill
Lydia R Wade
William R Clark
Aidan P Keelaghan
Daniel P Morris
Jonathan L McMurry
A real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.
description Cell-penetrating peptides (CPPs) are capable of transporting molecules to which they are tethered across cellular membranes. Unsurprisingly, CPPs have attracted attention for their potential drug delivery applications, but several technical hurdles remain to be overcome. Chief among them is the so-called 'endosomal escape problem,' i.e. the propensity of CPP-cargo molecules to be endocytosed but remain entrapped in endosomes rather than reaching the cytosol. Previously, a CPP fused to calmodulin that bound calmodulin binding site-containing cargos was shown to efficiently deliver cargos to the cytoplasm, effectively overcoming the endosomal escape problem. The CPP-adaptor, "TAT-CaM," evinces delivery at nM concentrations and more rapidly than we had previously been able to measure. To better understand the kinetics and mechanism of CPP-adaptor-mediated cargo delivery, a real-time cell penetrating assay was developed in which a flow chamber containing cultured cells was installed on the stage of a confocal microscope to allow for observation ab initio. Also examined in this study was an improved CPP-adaptor that utilizes naked mole rat (Heterocephalus glaber) calmodulin in place of human and results in superior internalization, likely due to its lesser net negative charge. Adaptor-cargo complexes were delivered into the flow chamber and fluorescence intensity in the midpoint of baby hamster kidney cells was measured as a function of time. Delivery of 400 nM cargo was observed within seven minutes and fluorescence continued to increase linearly as a function of time. Cargo-only control experiments showed that the minimal uptake which occurred independently of the CPP-adaptor resulted in punctate localization consistent with endosomal entrapment. A distance analysis was performed for cell-penetration experiments in which CPP-adaptor-delivered cargo showing wider dispersions throughout cells as compared to an analogous covalently-bound CPP-cargo. Small molecule endocytosis inhibitors did not have significant effects upon delivery. The real-time assay is an improvement upon static endpoint assays and should be informative in a broad array of applications.
format article
author Schuyler B Gentry
Scott J Nowak
Xuelei Ni
Stephanie A Hill
Lydia R Wade
William R Clark
Aidan P Keelaghan
Daniel P Morris
Jonathan L McMurry
author_facet Schuyler B Gentry
Scott J Nowak
Xuelei Ni
Stephanie A Hill
Lydia R Wade
William R Clark
Aidan P Keelaghan
Daniel P Morris
Jonathan L McMurry
author_sort Schuyler B Gentry
title A real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.
title_short A real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.
title_full A real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.
title_fullStr A real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.
title_full_unstemmed A real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.
title_sort real-time assay for cell-penetrating peptide-mediated delivery of molecular cargos.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/9451a358a4f44d599a4c82ed713d4cea
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