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Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore

There are still unmet needs in finding new technologies for biomedical diagnostic and industrial applications. A technology allowing the analysis of size and sequence of short peptide molecules of only few molecular copies is still challenging. The fast, low-cost and label-free single-molecule nanop...

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Autores principales: Piguet, Fabien, Ouldali, Hadjer, Pastoriza-Gallego, Manuela, Manivet, Philippe, Pelta, Juan, Oukhaled, Abdelghani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840376/
https://www.ncbi.nlm.nih.gov/pubmed/29511176
http://dx.doi.org/10.1038/s41467-018-03418-2
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author Piguet, Fabien
Ouldali, Hadjer
Pastoriza-Gallego, Manuela
Manivet, Philippe
Pelta, Juan
Oukhaled, Abdelghani
author_facet Piguet, Fabien
Ouldali, Hadjer
Pastoriza-Gallego, Manuela
Manivet, Philippe
Pelta, Juan
Oukhaled, Abdelghani
author_sort Piguet, Fabien
collection PubMed
description There are still unmet needs in finding new technologies for biomedical diagnostic and industrial applications. A technology allowing the analysis of size and sequence of short peptide molecules of only few molecular copies is still challenging. The fast, low-cost and label-free single-molecule nanopore technology could be an alternative for addressing these critical issues. Here, we demonstrate that the wild-type aerolysin nanopore enables the size-discrimination of several short uniformly charged homopeptides, mixed in solution, with a single amino acid resolution. Our system is very sensitive, allowing detecting and characterizing a few dozens of peptide impurities in a high purity commercial peptide sample, while conventional analysis techniques fail to do so.
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spelling pubmed-58403762018-03-09 Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore Piguet, Fabien Ouldali, Hadjer Pastoriza-Gallego, Manuela Manivet, Philippe Pelta, Juan Oukhaled, Abdelghani Nat Commun Article There are still unmet needs in finding new technologies for biomedical diagnostic and industrial applications. A technology allowing the analysis of size and sequence of short peptide molecules of only few molecular copies is still challenging. The fast, low-cost and label-free single-molecule nanopore technology could be an alternative for addressing these critical issues. Here, we demonstrate that the wild-type aerolysin nanopore enables the size-discrimination of several short uniformly charged homopeptides, mixed in solution, with a single amino acid resolution. Our system is very sensitive, allowing detecting and characterizing a few dozens of peptide impurities in a high purity commercial peptide sample, while conventional analysis techniques fail to do so. Nature Publishing Group UK 2018-03-06 /pmc/articles/PMC5840376/ /pubmed/29511176 http://dx.doi.org/10.1038/s41467-018-03418-2 Text en © The Author(s) 2018 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
Piguet, Fabien
Ouldali, Hadjer
Pastoriza-Gallego, Manuela
Manivet, Philippe
Pelta, Juan
Oukhaled, Abdelghani
Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore
title Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore
title_full Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore
title_fullStr Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore
title_full_unstemmed Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore
title_short Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore
title_sort identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840376/
https://www.ncbi.nlm.nih.gov/pubmed/29511176
http://dx.doi.org/10.1038/s41467-018-03418-2
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