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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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Detalles Bibliográficos
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
Descripción
Sumario: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.