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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6631817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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