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A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells
BACKGROUND: Nanoparticles’ intracellular fate requires proper internalization. Most cells make use of a battery of internalization pathways, but some are practically sealed, as they lack the biochemical machinery for cellular intake. Non-endocytic cells, such as mammals’ spermatozoa, challenge stand...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276607/ https://www.ncbi.nlm.nih.gov/pubmed/30568446 http://dx.doi.org/10.2147/IJN.S168149 |
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author | Berberian, Maria Victoria Pocognoni, Cristian A Mayorga, Luis S |
author_facet | Berberian, Maria Victoria Pocognoni, Cristian A Mayorga, Luis S |
author_sort | Berberian, Maria Victoria |
collection | PubMed |
description | BACKGROUND: Nanoparticles’ intracellular fate requires proper internalization. Most cells make use of a battery of internalization pathways, but some are practically sealed, as they lack the biochemical machinery for cellular intake. Non-endocytic cells, such as mammals’ spermatozoa, challenge standard drug-delivery strategies. PURPOSE: In this article, we present a gold nanoprobe that permeates the external and internal membranes of human sperm. METHODS: Our design makes use of a gold nanoparticle functionalized with a membrane-permeable cysteine-rich recombinant protein. The chimeric protein contains two units of physiologically active metallothioneins (MT) that also provide binding motifs to gold and a cell-penetrating-peptide sequence (CPP) that confers cell permeability to the nanoparticle. RESULTS: Transmission electron microscopy, indirect immunofluorescence, and functional assays show that the nanoprobe is readily internalized in sperm, without compromising cell integrity, while preserving MT’s physiological activity. Our findings highlight the potential of CPP-functionalized nanogold for investigating the physiology of otherwise impermeable non-endocytic cells. |
format | Online Article Text |
id | pubmed-6276607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62766072018-12-19 A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells Berberian, Maria Victoria Pocognoni, Cristian A Mayorga, Luis S Int J Nanomedicine Original Research BACKGROUND: Nanoparticles’ intracellular fate requires proper internalization. Most cells make use of a battery of internalization pathways, but some are practically sealed, as they lack the biochemical machinery for cellular intake. Non-endocytic cells, such as mammals’ spermatozoa, challenge standard drug-delivery strategies. PURPOSE: In this article, we present a gold nanoprobe that permeates the external and internal membranes of human sperm. METHODS: Our design makes use of a gold nanoparticle functionalized with a membrane-permeable cysteine-rich recombinant protein. The chimeric protein contains two units of physiologically active metallothioneins (MT) that also provide binding motifs to gold and a cell-penetrating-peptide sequence (CPP) that confers cell permeability to the nanoparticle. RESULTS: Transmission electron microscopy, indirect immunofluorescence, and functional assays show that the nanoprobe is readily internalized in sperm, without compromising cell integrity, while preserving MT’s physiological activity. Our findings highlight the potential of CPP-functionalized nanogold for investigating the physiology of otherwise impermeable non-endocytic cells. Dove Medical Press 2018-11-28 /pmc/articles/PMC6276607/ /pubmed/30568446 http://dx.doi.org/10.2147/IJN.S168149 Text en © 2018 Berberian et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Berberian, Maria Victoria Pocognoni, Cristian A Mayorga, Luis S A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells |
title | A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells |
title_full | A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells |
title_fullStr | A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells |
title_full_unstemmed | A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells |
title_short | A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells |
title_sort | tem-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276607/ https://www.ncbi.nlm.nih.gov/pubmed/30568446 http://dx.doi.org/10.2147/IJN.S168149 |
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