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Super-resolution Imaging of Structure, Molecular Composition, and Stability of Single Oligonucleotide Polyplexes
[Image: see text] The successful application of gene therapy relies on the development of safe and efficient delivery vectors. Cationic polymers such as cell-penetrating peptides (CPPs) can condense genetic material into nanoscale particles, called polyplexes, and induce cellular uptake. With respec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509642/ https://www.ncbi.nlm.nih.gov/pubmed/31001985 http://dx.doi.org/10.1021/acs.nanolett.8b04407 |
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author | Feiner-Gracia, Natalia Olea, R. Alis Fitzner, Robert El Boujnouni, Najoua van Asbeck, Alexander H. Brock, Roland Albertazzi, Lorenzo |
author_facet | Feiner-Gracia, Natalia Olea, R. Alis Fitzner, Robert El Boujnouni, Najoua van Asbeck, Alexander H. Brock, Roland Albertazzi, Lorenzo |
author_sort | Feiner-Gracia, Natalia |
collection | PubMed |
description | [Image: see text] The successful application of gene therapy relies on the development of safe and efficient delivery vectors. Cationic polymers such as cell-penetrating peptides (CPPs) can condense genetic material into nanoscale particles, called polyplexes, and induce cellular uptake. With respect to this point, several aspects of the nanoscale structure of polyplexes have remained elusive because of the difficulty in visualizing the molecular arrangement of the two components with nanometer resolution. This limitation has hampered the rational design of polyplexes based on direct structural information. Here, we used super-resolution imaging to study the structure and molecular composition of individual CPP-mRNA polyplexes with nanometer accuracy. We use two-color direct stochastic optical reconstruction microscopy (dSTORM) to unveil the impact of peptide stoichiometry on polyplex structure and composition and to assess their destabilization in blood serum. Our method provides information about the size and composition of individual polyplexes, allowing the study of such properties on a single polyplex basis. Furthermore, the differences in stoichiometry readily explain the differences in cellular uptake behavior. Thus, quantitative dSTORM of polyplexes is complementary to the currently used characterization techniques for understanding the determinants of polyplex activity in vitro and inside cells. |
format | Online Article Text |
id | pubmed-6509642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65096422019-05-13 Super-resolution Imaging of Structure, Molecular Composition, and Stability of Single Oligonucleotide Polyplexes Feiner-Gracia, Natalia Olea, R. Alis Fitzner, Robert El Boujnouni, Najoua van Asbeck, Alexander H. Brock, Roland Albertazzi, Lorenzo Nano Lett [Image: see text] The successful application of gene therapy relies on the development of safe and efficient delivery vectors. Cationic polymers such as cell-penetrating peptides (CPPs) can condense genetic material into nanoscale particles, called polyplexes, and induce cellular uptake. With respect to this point, several aspects of the nanoscale structure of polyplexes have remained elusive because of the difficulty in visualizing the molecular arrangement of the two components with nanometer resolution. This limitation has hampered the rational design of polyplexes based on direct structural information. Here, we used super-resolution imaging to study the structure and molecular composition of individual CPP-mRNA polyplexes with nanometer accuracy. We use two-color direct stochastic optical reconstruction microscopy (dSTORM) to unveil the impact of peptide stoichiometry on polyplex structure and composition and to assess their destabilization in blood serum. Our method provides information about the size and composition of individual polyplexes, allowing the study of such properties on a single polyplex basis. Furthermore, the differences in stoichiometry readily explain the differences in cellular uptake behavior. Thus, quantitative dSTORM of polyplexes is complementary to the currently used characterization techniques for understanding the determinants of polyplex activity in vitro and inside cells. American Chemical Society 2019-04-19 2019-05-08 /pmc/articles/PMC6509642/ /pubmed/31001985 http://dx.doi.org/10.1021/acs.nanolett.8b04407 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Feiner-Gracia, Natalia Olea, R. Alis Fitzner, Robert El Boujnouni, Najoua van Asbeck, Alexander H. Brock, Roland Albertazzi, Lorenzo Super-resolution Imaging of Structure, Molecular Composition, and Stability of Single Oligonucleotide Polyplexes |
title | Super-resolution Imaging of Structure, Molecular Composition,
and Stability of Single Oligonucleotide Polyplexes |
title_full | Super-resolution Imaging of Structure, Molecular Composition,
and Stability of Single Oligonucleotide Polyplexes |
title_fullStr | Super-resolution Imaging of Structure, Molecular Composition,
and Stability of Single Oligonucleotide Polyplexes |
title_full_unstemmed | Super-resolution Imaging of Structure, Molecular Composition,
and Stability of Single Oligonucleotide Polyplexes |
title_short | Super-resolution Imaging of Structure, Molecular Composition,
and Stability of Single Oligonucleotide Polyplexes |
title_sort | super-resolution imaging of structure, molecular composition,
and stability of single oligonucleotide polyplexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509642/ https://www.ncbi.nlm.nih.gov/pubmed/31001985 http://dx.doi.org/10.1021/acs.nanolett.8b04407 |
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