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Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue
The cytosolic delivery of various substrates in 3D multicellular spheroids by thiol-mediated uptake is reported. This is important because most orthodox systems, including polycationic cell-penetrating peptides, fail to deliver efficiently into deep tissue. The grand principles of supramolecular che...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549803/ https://www.ncbi.nlm.nih.gov/pubmed/34760179 http://dx.doi.org/10.1039/d1sc04828g |
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author | Martinent, Rémi Tawffik, Salman López-Andarias, Javier Moreau, Dimitri Laurent, Quentin Matile, Stefan |
author_facet | Martinent, Rémi Tawffik, Salman López-Andarias, Javier Moreau, Dimitri Laurent, Quentin Matile, Stefan |
author_sort | Martinent, Rémi |
collection | PubMed |
description | The cytosolic delivery of various substrates in 3D multicellular spheroids by thiol-mediated uptake is reported. This is important because most orthodox systems, including polycationic cell-penetrating peptides, fail to deliver efficiently into deep tissue. The grand principles of supramolecular chemistry, that is the pH dependence of dynamic covalent disulfide exchange with known thiols on the transferrin receptor, are proposed to account for transcytosis into deep tissue, while the known but elusive exchange cascades along the same or other partners assure cytosolic delivery in kinetic competition. For quantitative detection in the cytosol, the 2D chloroalkane penetration assay (CAPA) is translated to 3D deep tissue. The targeted delivery of quantum dots, otherwise already troublesome in 2D culture, and the controlled release of mechanophores are realized to exemplify the power of thiol-mediated uptake into spheroids. As transporters, dithiolane quartets on streptavidin templates are introduced as modular motifs. Built from two amino acids only, the varied stereochemistry and peptide sequence are shown to cover maximal functional space with minimal structural change, i.e., constitutional isomers. Reviving a classic in peptide chemistry, this templated assembly of β quartets promises to expand streptavidin biotechnology in new directions, while the discovery of general cytosolic delivery in deep tissue as an intrinsic advantage further enhances the significance and usefulness of thiol-mediated uptake. |
format | Online Article Text |
id | pubmed-8549803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-85498032021-11-09 Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue Martinent, Rémi Tawffik, Salman López-Andarias, Javier Moreau, Dimitri Laurent, Quentin Matile, Stefan Chem Sci Chemistry The cytosolic delivery of various substrates in 3D multicellular spheroids by thiol-mediated uptake is reported. This is important because most orthodox systems, including polycationic cell-penetrating peptides, fail to deliver efficiently into deep tissue. The grand principles of supramolecular chemistry, that is the pH dependence of dynamic covalent disulfide exchange with known thiols on the transferrin receptor, are proposed to account for transcytosis into deep tissue, while the known but elusive exchange cascades along the same or other partners assure cytosolic delivery in kinetic competition. For quantitative detection in the cytosol, the 2D chloroalkane penetration assay (CAPA) is translated to 3D deep tissue. The targeted delivery of quantum dots, otherwise already troublesome in 2D culture, and the controlled release of mechanophores are realized to exemplify the power of thiol-mediated uptake into spheroids. As transporters, dithiolane quartets on streptavidin templates are introduced as modular motifs. Built from two amino acids only, the varied stereochemistry and peptide sequence are shown to cover maximal functional space with minimal structural change, i.e., constitutional isomers. Reviving a classic in peptide chemistry, this templated assembly of β quartets promises to expand streptavidin biotechnology in new directions, while the discovery of general cytosolic delivery in deep tissue as an intrinsic advantage further enhances the significance and usefulness of thiol-mediated uptake. The Royal Society of Chemistry 2021-10-06 /pmc/articles/PMC8549803/ /pubmed/34760179 http://dx.doi.org/10.1039/d1sc04828g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Martinent, Rémi Tawffik, Salman López-Andarias, Javier Moreau, Dimitri Laurent, Quentin Matile, Stefan Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue |
title | Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue |
title_full | Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue |
title_fullStr | Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue |
title_full_unstemmed | Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue |
title_short | Dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue |
title_sort | dithiolane quartets: thiol-mediated uptake enables cytosolic delivery in deep tissue |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549803/ https://www.ncbi.nlm.nih.gov/pubmed/34760179 http://dx.doi.org/10.1039/d1sc04828g |
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