Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo

Abstract The transport of membrane impermeable compounds into cells is a prerequisite for the efficient cellular delivery of hydrophilic and amphiphilic compounds and drugs. Transport into the cell's cytosolic compartment should ideally be controllable and it should involve biologically compati...

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Main Authors: Sergej Kudruk, Sharafudheen Pottanam Chali, Anna Livia Linard Matos, Cole Bourque, Clara Dunker, Christos Gatsogiannis, Bart Jan Ravoo, Volker Gerke
Format: Article
Language:English
Published: Wiley 2021-09-01
Series:Advanced Science
Subjects:
Online Access:https://doi.org/10.1002/advs.202100694
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spelling doaj-78b828752c804bfda93d46a2fab4da6a2021-09-22T07:57:32ZengWileyAdvanced Science2198-38442021-09-01818n/an/a10.1002/advs.202100694Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable CargoSergej Kudruk0Sharafudheen Pottanam Chali1Anna Livia Linard Matos2Cole Bourque3Clara Dunker4Christos Gatsogiannis5Bart Jan Ravoo6Volker Gerke7Institute of Medical Biochemistry Center for Molecular Biology of Inflammation University of Muenster Von‐Esmarch‐Str. 56 Münster 48149 GermanyCenter for Soft Nanoscience and Organic Chemistry Institute University of Muenster Busso Peus Straße 10 Münster 48149 GermanyInstitute of Medical Biochemistry Center for Molecular Biology of Inflammation University of Muenster Von‐Esmarch‐Str. 56 Münster 48149 GermanyCenter for Soft Nanoscience and Institute of Medical Physics and Biophysics University of Muenster Busso Peus Straße 10 Münster 48149 GermanyInstitute of Medical Biochemistry Center for Molecular Biology of Inflammation University of Muenster Von‐Esmarch‐Str. 56 Münster 48149 GermanyCenter for Soft Nanoscience and Institute of Medical Physics and Biophysics University of Muenster Busso Peus Straße 10 Münster 48149 GermanyCenter for Soft Nanoscience and Organic Chemistry Institute University of Muenster Busso Peus Straße 10 Münster 48149 GermanyInstitute of Medical Biochemistry Center for Molecular Biology of Inflammation University of Muenster Von‐Esmarch‐Str. 56 Münster 48149 GermanyAbstract The transport of membrane impermeable compounds into cells is a prerequisite for the efficient cellular delivery of hydrophilic and amphiphilic compounds and drugs. Transport into the cell's cytosolic compartment should ideally be controllable and it should involve biologically compatible and degradable vehicles. Addressing these challenges, nanocontainers based on cyclodextrin amphiphiles that are stabilized by a biodegradable peptide shell are developed and their potential to deliver fluorescently labeled cargo into human cells is analyzed. Host–guest mediated self‐assembly of a thiol‐containing short peptide or a cystamine‐cross‐linked polypeptide shell on cyclodextrin vesicles produce short peptide‐shelled (SPSVss) or polypeptide‐shelled vesicles (PPSVss), respectively, with redox‐responsive and biodegradable features. Whereas SPSVss are permeable and less stable, PPSVss effectively encapsulate cargo and show a strictly regulated release of membrane impermeable cargo triggered by either reducing conditions or peptidase treatment. Live cell experiments reveal that the novel PPSVSS are readily internalized by primary human endothelial cells (human umbilical vein endothelial cells) and cervical cancer cells and that the reductive microenvironment of the cells’ endosomes trigger release of the hydrophilic cargo into the cytosol. Thus, PPSVSS represent a highly efficient, biodegradable, and tunable system for overcoming the plasma membrane as a natural barrier for membrane‐impermeable cargo.https://doi.org/10.1002/advs.202100694biodegradablecyclodextrindual‐responsiveintracellular deliverypolypeptides
collection DOAJ
language English
format Article
sources DOAJ
author Sergej Kudruk
Sharafudheen Pottanam Chali
Anna Livia Linard Matos
Cole Bourque
Clara Dunker
Christos Gatsogiannis
Bart Jan Ravoo
Volker Gerke
spellingShingle Sergej Kudruk
Sharafudheen Pottanam Chali
Anna Livia Linard Matos
Cole Bourque
Clara Dunker
Christos Gatsogiannis
Bart Jan Ravoo
Volker Gerke
Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo
Advanced Science
biodegradable
cyclodextrin
dual‐responsive
intracellular delivery
polypeptides
author_facet Sergej Kudruk
Sharafudheen Pottanam Chali
Anna Livia Linard Matos
Cole Bourque
Clara Dunker
Christos Gatsogiannis
Bart Jan Ravoo
Volker Gerke
author_sort Sergej Kudruk
title Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo
title_short Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo
title_full Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo
title_fullStr Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo
title_full_unstemmed Biodegradable and Dual‐Responsive Polypeptide‐Shelled Cyclodextrin‐Containers for Intracellular Delivery of Membrane‐Impermeable Cargo
title_sort biodegradable and dual‐responsive polypeptide‐shelled cyclodextrin‐containers for intracellular delivery of membrane‐impermeable cargo
publisher Wiley
series Advanced Science
issn 2198-3844
publishDate 2021-09-01
description Abstract The transport of membrane impermeable compounds into cells is a prerequisite for the efficient cellular delivery of hydrophilic and amphiphilic compounds and drugs. Transport into the cell's cytosolic compartment should ideally be controllable and it should involve biologically compatible and degradable vehicles. Addressing these challenges, nanocontainers based on cyclodextrin amphiphiles that are stabilized by a biodegradable peptide shell are developed and their potential to deliver fluorescently labeled cargo into human cells is analyzed. Host–guest mediated self‐assembly of a thiol‐containing short peptide or a cystamine‐cross‐linked polypeptide shell on cyclodextrin vesicles produce short peptide‐shelled (SPSVss) or polypeptide‐shelled vesicles (PPSVss), respectively, with redox‐responsive and biodegradable features. Whereas SPSVss are permeable and less stable, PPSVss effectively encapsulate cargo and show a strictly regulated release of membrane impermeable cargo triggered by either reducing conditions or peptidase treatment. Live cell experiments reveal that the novel PPSVSS are readily internalized by primary human endothelial cells (human umbilical vein endothelial cells) and cervical cancer cells and that the reductive microenvironment of the cells’ endosomes trigger release of the hydrophilic cargo into the cytosol. Thus, PPSVSS represent a highly efficient, biodegradable, and tunable system for overcoming the plasma membrane as a natural barrier for membrane‐impermeable cargo.
topic biodegradable
cyclodextrin
dual‐responsive
intracellular delivery
polypeptides
url https://doi.org/10.1002/advs.202100694
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