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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.
Afiliación
  • Piguet F; LAMBE UMR 8587, Université de Cergy-Pontoise, 95300, Pontoise, France. fabien.piguet@u-cergy.fr.
  • Ouldali H; LAMBE UMR 8587, Université de Cergy-Pontoise, 95300, Pontoise, France.
  • Pastoriza-Gallego M; LAMBE UMR 8587, Université de Cergy-Pontoise, 95300, Pontoise, France.
  • Manivet P; APHP, Centre de Ressources Biologiques BB-0033-00064, Plateforme de Bio-Pathologie et de Technologies Innovantes en santé, Hôpital Lariboisière, 75010, Paris, France.
  • Pelta J; INSERM UMR-S942, Hôpital Lariboisière, 75010, Paris, France.
  • Oukhaled A; LAMBE UMR 8587, Université d'Evry-Val-d'Essonne, 91000, Evry, France. juan.pelta@univ-evry.fr.
Nat Commun ; 9(1): 966, 2018 03 06.
Article en En | MEDLINE | ID: mdl-29511176
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Toxinas Bacterianas / Proteínas Citotóxicas Formadoras de Poros Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Toxinas Bacterianas / Proteínas Citotóxicas Formadoras de Poros Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido