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Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions

Peptide microarrays are a fast-developing field enabling the mapping of linear epitopes in the immune response to vaccinations or diseases and high throughput studying of protein-protein interactions. In this respect, a rapid label-free measurement of protein layer topographies in the array format i...

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Autores principales: Palermo, Andrea, Thelen, Richard, Weber, Laura K., Foertsch, Tobias, Rentschler, Simone, Hackert, Verena, Syurik, Julia, Nesterov-Mueller, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631817/
https://www.ncbi.nlm.nih.gov/pubmed/30934705
http://dx.doi.org/10.3390/ht8020007
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author Palermo, Andrea
Thelen, Richard
Weber, Laura K.
Foertsch, Tobias
Rentschler, Simone
Hackert, Verena
Syurik, Julia
Nesterov-Mueller, Alexander
author_facet Palermo, Andrea
Thelen, Richard
Weber, Laura K.
Foertsch, Tobias
Rentschler, Simone
Hackert, Verena
Syurik, Julia
Nesterov-Mueller, Alexander
author_sort Palermo, Andrea
collection PubMed
description Peptide microarrays are a fast-developing field enabling the mapping of linear epitopes in the immune response to vaccinations or diseases and high throughput studying of protein-protein interactions. In this respect, a rapid label-free measurement of protein layer topographies in the array format is of great interest but is also a great challenge due to the extremely low aspect ratios of the peptide spots. We have demonstrated the potential of vertical scanning interferometry (VSI) for a detailed morphological analysis of peptide arrays and binding antibodies. The VSI technique is shown to scan an array area of 5.1 square millimeters within 3–4 min at a resolution of 1.4 μm lateral and 0.1 nm vertical in the full automation mode. Topographies obtained by VSI do match the one obtained by AFM measurements, demonstrating the accuracy of the technique. A detailed topology of peptide-antibody layers on single spots was measured. Two different measurement regions are distinguished according to the antibody concentration. In the case of weakly diluted serum, the thickness of the antibody layer is independent of the serum dilution and corresponds to the physical thickness of the accumulated antibody layer. In strongly diluted serum, the thickness measured via VSI is linearly proportional to the serum dilution.
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spelling pubmed-66318172019-08-19 Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions Palermo, Andrea Thelen, Richard Weber, Laura K. Foertsch, Tobias Rentschler, Simone Hackert, Verena Syurik, Julia Nesterov-Mueller, Alexander High Throughput Article Peptide microarrays are a fast-developing field enabling the mapping of linear epitopes in the immune response to vaccinations or diseases and high throughput studying of protein-protein interactions. In this respect, a rapid label-free measurement of protein layer topographies in the array format is of great interest but is also a great challenge due to the extremely low aspect ratios of the peptide spots. We have demonstrated the potential of vertical scanning interferometry (VSI) for a detailed morphological analysis of peptide arrays and binding antibodies. The VSI technique is shown to scan an array area of 5.1 square millimeters within 3–4 min at a resolution of 1.4 μm lateral and 0.1 nm vertical in the full automation mode. Topographies obtained by VSI do match the one obtained by AFM measurements, demonstrating the accuracy of the technique. A detailed topology of peptide-antibody layers on single spots was measured. Two different measurement regions are distinguished according to the antibody concentration. In the case of weakly diluted serum, the thickness of the antibody layer is independent of the serum dilution and corresponds to the physical thickness of the accumulated antibody layer. In strongly diluted serum, the thickness measured via VSI is linearly proportional to the serum dilution. MDPI 2019-03-27 /pmc/articles/PMC6631817/ /pubmed/30934705 http://dx.doi.org/10.3390/ht8020007 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Palermo, Andrea
Thelen, Richard
Weber, Laura K.
Foertsch, Tobias
Rentschler, Simone
Hackert, Verena
Syurik, Julia
Nesterov-Mueller, Alexander
Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions
title Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions
title_full Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions
title_fullStr Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions
title_full_unstemmed Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions
title_short Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions
title_sort vertical scanning interferometry for label-free detection of peptide-antibody interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631817/
https://www.ncbi.nlm.nih.gov/pubmed/30934705
http://dx.doi.org/10.3390/ht8020007
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