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BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood
Systemic blood stream infections are a major threat to human health and are dramatically increasing worldwide. Pseudomonas aeruginosa is a WHO-alerted multi-resistant pathogen of extreme importance as a cause of sepsis. Septicemia patients have significantly increased survival chances if sepsis is d...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537436/ https://www.ncbi.nlm.nih.gov/pubmed/34681780 http://dx.doi.org/10.3390/ijms222011118 |
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author | Krämer, Markus Kissmann, Ann-Kathrin Raber, Heinz Fabian Xing, Hu Favella, Patrizia Müller, Ingrid Spellerberg, Barbara Weil, Tanja Kubiczek, Dennis Sihler, Susanne Ziener, Ulrich Rosenau, Frank |
author_facet | Krämer, Markus Kissmann, Ann-Kathrin Raber, Heinz Fabian Xing, Hu Favella, Patrizia Müller, Ingrid Spellerberg, Barbara Weil, Tanja Kubiczek, Dennis Sihler, Susanne Ziener, Ulrich Rosenau, Frank |
author_sort | Krämer, Markus |
collection | PubMed |
description | Systemic blood stream infections are a major threat to human health and are dramatically increasing worldwide. Pseudomonas aeruginosa is a WHO-alerted multi-resistant pathogen of extreme importance as a cause of sepsis. Septicemia patients have significantly increased survival chances if sepsis is diagnosed in the early stages. Affinity materials can not only represent attractive tools for specific diagnostics of pathogens in the blood but can prospectively also serve as the technical foundation of therapeutic filtration devices. Based on the recently developed aptamers directed against P. aeruginosa, we here present aptamer-functionalized beads for specific binding of this pathogen in blood samples. These aptamer capture beads (ACBs) are manufactured by crosslinking bovine serum albumin (BSA) in an emulsion and subsequent functionalization with the amino-modified aptamers on the bead surface using the thiol- and amino-reactive bispecific crosslinker PEG(4)-SPDP. Specific and quantitative binding of P. aeruginosa as the dedicated target of the ACBs was demonstrated in serum and blood. These initial but promising results may open new routes for the development of ACBs as a platform technology for fast and reliable diagnosis of bloodstream infections and, in the long term, blood filtration techniques in the fight against sepsis. |
format | Online Article Text |
id | pubmed-8537436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85374362021-10-24 BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood Krämer, Markus Kissmann, Ann-Kathrin Raber, Heinz Fabian Xing, Hu Favella, Patrizia Müller, Ingrid Spellerberg, Barbara Weil, Tanja Kubiczek, Dennis Sihler, Susanne Ziener, Ulrich Rosenau, Frank Int J Mol Sci Article Systemic blood stream infections are a major threat to human health and are dramatically increasing worldwide. Pseudomonas aeruginosa is a WHO-alerted multi-resistant pathogen of extreme importance as a cause of sepsis. Septicemia patients have significantly increased survival chances if sepsis is diagnosed in the early stages. Affinity materials can not only represent attractive tools for specific diagnostics of pathogens in the blood but can prospectively also serve as the technical foundation of therapeutic filtration devices. Based on the recently developed aptamers directed against P. aeruginosa, we here present aptamer-functionalized beads for specific binding of this pathogen in blood samples. These aptamer capture beads (ACBs) are manufactured by crosslinking bovine serum albumin (BSA) in an emulsion and subsequent functionalization with the amino-modified aptamers on the bead surface using the thiol- and amino-reactive bispecific crosslinker PEG(4)-SPDP. Specific and quantitative binding of P. aeruginosa as the dedicated target of the ACBs was demonstrated in serum and blood. These initial but promising results may open new routes for the development of ACBs as a platform technology for fast and reliable diagnosis of bloodstream infections and, in the long term, blood filtration techniques in the fight against sepsis. MDPI 2021-10-15 /pmc/articles/PMC8537436/ /pubmed/34681780 http://dx.doi.org/10.3390/ijms222011118 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Krämer, Markus Kissmann, Ann-Kathrin Raber, Heinz Fabian Xing, Hu Favella, Patrizia Müller, Ingrid Spellerberg, Barbara Weil, Tanja Kubiczek, Dennis Sihler, Susanne Ziener, Ulrich Rosenau, Frank BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood |
title | BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood |
title_full | BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood |
title_fullStr | BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood |
title_full_unstemmed | BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood |
title_short | BSA Hydrogel Beads Functionalized with a Specific Aptamer Library for Capturing Pseudomonas aeruginosa in Serum and Blood |
title_sort | bsa hydrogel beads functionalized with a specific aptamer library for capturing pseudomonas aeruginosa in serum and blood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537436/ https://www.ncbi.nlm.nih.gov/pubmed/34681780 http://dx.doi.org/10.3390/ijms222011118 |
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