Cargando…
Two-tier supramolecular encapsulation of small molecules in a protein cage
Expanding protein design to include other molecular building blocks has the potential to increase structural complexity and practical utility. Nature often employs hybrid systems, such as clathrin-coated vesicles, lipid droplets, and lipoproteins, which combine biopolymers and lipids to transport a...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588467/ https://www.ncbi.nlm.nih.gov/pubmed/33106476 http://dx.doi.org/10.1038/s41467-020-19112-1 |
_version_ | 1783600378580828160 |
---|---|
author | Edwardson, Thomas G. W. Tetter, Stephan Hilvert, Donald |
author_facet | Edwardson, Thomas G. W. Tetter, Stephan Hilvert, Donald |
author_sort | Edwardson, Thomas G. W. |
collection | PubMed |
description | Expanding protein design to include other molecular building blocks has the potential to increase structural complexity and practical utility. Nature often employs hybrid systems, such as clathrin-coated vesicles, lipid droplets, and lipoproteins, which combine biopolymers and lipids to transport a broader range of cargo molecules. To recapitulate the structure and function of such composite compartments, we devised a supramolecular strategy that enables porous protein cages to encapsulate poorly water-soluble small molecule cargo through templated formation of a hydrophobic surfactant-based core. These lipoprotein-like complexes protect their cargo from sequestration by serum proteins and enhance the cellular uptake of fluorescent probes and cytotoxic drugs. This design concept could be applied to other protein cages, surfactant mixtures, and cargo molecules to generate unique hybrid architectures and functional capabilities. |
format | Online Article Text |
id | pubmed-7588467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75884672020-11-10 Two-tier supramolecular encapsulation of small molecules in a protein cage Edwardson, Thomas G. W. Tetter, Stephan Hilvert, Donald Nat Commun Article Expanding protein design to include other molecular building blocks has the potential to increase structural complexity and practical utility. Nature often employs hybrid systems, such as clathrin-coated vesicles, lipid droplets, and lipoproteins, which combine biopolymers and lipids to transport a broader range of cargo molecules. To recapitulate the structure and function of such composite compartments, we devised a supramolecular strategy that enables porous protein cages to encapsulate poorly water-soluble small molecule cargo through templated formation of a hydrophobic surfactant-based core. These lipoprotein-like complexes protect their cargo from sequestration by serum proteins and enhance the cellular uptake of fluorescent probes and cytotoxic drugs. This design concept could be applied to other protein cages, surfactant mixtures, and cargo molecules to generate unique hybrid architectures and functional capabilities. Nature Publishing Group UK 2020-10-26 /pmc/articles/PMC7588467/ /pubmed/33106476 http://dx.doi.org/10.1038/s41467-020-19112-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Edwardson, Thomas G. W. Tetter, Stephan Hilvert, Donald Two-tier supramolecular encapsulation of small molecules in a protein cage |
title | Two-tier supramolecular encapsulation of small molecules in a protein cage |
title_full | Two-tier supramolecular encapsulation of small molecules in a protein cage |
title_fullStr | Two-tier supramolecular encapsulation of small molecules in a protein cage |
title_full_unstemmed | Two-tier supramolecular encapsulation of small molecules in a protein cage |
title_short | Two-tier supramolecular encapsulation of small molecules in a protein cage |
title_sort | two-tier supramolecular encapsulation of small molecules in a protein cage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588467/ https://www.ncbi.nlm.nih.gov/pubmed/33106476 http://dx.doi.org/10.1038/s41467-020-19112-1 |
work_keys_str_mv | AT edwardsonthomasgw twotiersupramolecularencapsulationofsmallmoleculesinaproteincage AT tetterstephan twotiersupramolecularencapsulationofsmallmoleculesinaproteincage AT hilvertdonald twotiersupramolecularencapsulationofsmallmoleculesinaproteincage |