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Biomimetic Mineralization of Iron-Fumarate Nanoparticles for Protective Encapsulation and Intracellular Delivery of Proteins
[Image: see text] Biomimetic mineralization of proteins and nucleic acids into hybrid metal−organic nanoparticles allows for protection and cellular delivery of these sensitive and generally membrane-impermeable biomolecules. Although the concept is not necessarily restricted to zeolitic imidazolate...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558304/ https://www.ncbi.nlm.nih.gov/pubmed/36248226 http://dx.doi.org/10.1021/acs.chemmater.2c01736 |
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author | Mirzazadeh Dizaji, Negar Lin, Yi Bein, Thomas Wagner, Ernst Wuttke, Stefan Lächelt, Ulrich Engelke, Hanna |
author_facet | Mirzazadeh Dizaji, Negar Lin, Yi Bein, Thomas Wagner, Ernst Wuttke, Stefan Lächelt, Ulrich Engelke, Hanna |
author_sort | Mirzazadeh Dizaji, Negar |
collection | PubMed |
description | [Image: see text] Biomimetic mineralization of proteins and nucleic acids into hybrid metal−organic nanoparticles allows for protection and cellular delivery of these sensitive and generally membrane-impermeable biomolecules. Although the concept is not necessarily restricted to zeolitic imidazolate frameworks (ZIFs), so far reports about intracellular delivery of functional proteins have focused on ZIF structures. Here, we present a green room-temperature synthesis of amorphous iron-fumarate nanoparticles under mildly acidic conditions in water to encapsulate bovine serum albumin (BSA), horseradish peroxidase (HRP), green fluorescent protein (GFP), and Cas9/sgRNA ribonucleoproteins (RNPs). The synthesis conditions preserve the activity of enzymatic model proteins and the resulting nanoparticles deliver functional HRP and Cas9 RNPs into cells. Incorporation into the iron-fumarate nanoparticles preserves and protects the activity of RNPs composed of the acid-sensitive Cas9 protein and hydrolytically labile RNA even during exposure to pH 3.5 and storage for 2 months at 4 °C, which are conditions that strongly impair the functionality of unprotected RNPs. Thus, the biomimetic mineralization into iron-fumarate nanoparticles presents a versatile platform for the delivery of biomolecules and protects them from degradation during storage under challenging conditions. |
format | Online Article Text |
id | pubmed-9558304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95583042022-10-14 Biomimetic Mineralization of Iron-Fumarate Nanoparticles for Protective Encapsulation and Intracellular Delivery of Proteins Mirzazadeh Dizaji, Negar Lin, Yi Bein, Thomas Wagner, Ernst Wuttke, Stefan Lächelt, Ulrich Engelke, Hanna Chem Mater [Image: see text] Biomimetic mineralization of proteins and nucleic acids into hybrid metal−organic nanoparticles allows for protection and cellular delivery of these sensitive and generally membrane-impermeable biomolecules. Although the concept is not necessarily restricted to zeolitic imidazolate frameworks (ZIFs), so far reports about intracellular delivery of functional proteins have focused on ZIF structures. Here, we present a green room-temperature synthesis of amorphous iron-fumarate nanoparticles under mildly acidic conditions in water to encapsulate bovine serum albumin (BSA), horseradish peroxidase (HRP), green fluorescent protein (GFP), and Cas9/sgRNA ribonucleoproteins (RNPs). The synthesis conditions preserve the activity of enzymatic model proteins and the resulting nanoparticles deliver functional HRP and Cas9 RNPs into cells. Incorporation into the iron-fumarate nanoparticles preserves and protects the activity of RNPs composed of the acid-sensitive Cas9 protein and hydrolytically labile RNA even during exposure to pH 3.5 and storage for 2 months at 4 °C, which are conditions that strongly impair the functionality of unprotected RNPs. Thus, the biomimetic mineralization into iron-fumarate nanoparticles presents a versatile platform for the delivery of biomolecules and protects them from degradation during storage under challenging conditions. American Chemical Society 2022-10-03 2022-10-11 /pmc/articles/PMC9558304/ /pubmed/36248226 http://dx.doi.org/10.1021/acs.chemmater.2c01736 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Mirzazadeh Dizaji, Negar Lin, Yi Bein, Thomas Wagner, Ernst Wuttke, Stefan Lächelt, Ulrich Engelke, Hanna Biomimetic Mineralization of Iron-Fumarate Nanoparticles for Protective Encapsulation and Intracellular Delivery of Proteins |
title | Biomimetic Mineralization of Iron-Fumarate Nanoparticles
for Protective Encapsulation and Intracellular Delivery of Proteins |
title_full | Biomimetic Mineralization of Iron-Fumarate Nanoparticles
for Protective Encapsulation and Intracellular Delivery of Proteins |
title_fullStr | Biomimetic Mineralization of Iron-Fumarate Nanoparticles
for Protective Encapsulation and Intracellular Delivery of Proteins |
title_full_unstemmed | Biomimetic Mineralization of Iron-Fumarate Nanoparticles
for Protective Encapsulation and Intracellular Delivery of Proteins |
title_short | Biomimetic Mineralization of Iron-Fumarate Nanoparticles
for Protective Encapsulation and Intracellular Delivery of Proteins |
title_sort | biomimetic mineralization of iron-fumarate nanoparticles
for protective encapsulation and intracellular delivery of proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558304/ https://www.ncbi.nlm.nih.gov/pubmed/36248226 http://dx.doi.org/10.1021/acs.chemmater.2c01736 |
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