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3D-Printed High-Pressure-Resistant Immobilized Enzyme Microreactor (μIMER) for Protein Analysis
[Image: see text] Additive manufacturing (3D printing) has greatly revolutionized the way researchers approach certain technical challenges. Despite its outstanding print quality and resolution, stereolithography (SLA) printing is cost-effective and relatively accessible. However, applications invol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218953/ https://www.ncbi.nlm.nih.gov/pubmed/35678765 http://dx.doi.org/10.1021/acs.analchem.1c05232 |
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author | Rainer, Tobias Egger, Anna-Sophia Zeindl, Ricarda Tollinger, Martin Kwiatkowski, Marcel Müller, Thomas |
author_facet | Rainer, Tobias Egger, Anna-Sophia Zeindl, Ricarda Tollinger, Martin Kwiatkowski, Marcel Müller, Thomas |
author_sort | Rainer, Tobias |
collection | PubMed |
description | [Image: see text] Additive manufacturing (3D printing) has greatly revolutionized the way researchers approach certain technical challenges. Despite its outstanding print quality and resolution, stereolithography (SLA) printing is cost-effective and relatively accessible. However, applications involving mass spectrometry (MS) are few due to residual oligomers and additives leaching from SLA-printed devices that interfere with MS analyses. We identified the crosslinking agent urethane dimethacrylate as the main contaminant derived from SLA prints. A stringent washing and post-curing protocol mitigated sample contamination and rendered SLA prints suitable for MS hyphenation. Thereafter, SLA printing was used to produce 360 μm I.D. microcolumn chips with excellent structural properties. By packing the column with polystyrene microspheres and covalently immobilizing pepsin, an exceptionally effective microscale immobilized enzyme reactor (μIMER) was created. Implemented in an online liquid chromatography-MS/MS setup, the protease microcolumn enabled reproducible protein digestion and peptide mapping with 100% sequence coverage obtained for three different recombinant proteins. Additionally, when assessing the μIMER digestion efficiency for complex proteome samples, it delivered a 144-fold faster and significantly more efficient protein digestion compared to 24 h for bulk digestion. The 3D-printed μIMER withstands remarkably high pressures above 130 bar and retains its activity for several weeks. This versatile platform will enable researchers to produce tailored polymer-based enzyme reactors for various applications in analytical chemistry and beyond. |
format | Online Article Text |
id | pubmed-9218953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92189532022-06-24 3D-Printed High-Pressure-Resistant Immobilized Enzyme Microreactor (μIMER) for Protein Analysis Rainer, Tobias Egger, Anna-Sophia Zeindl, Ricarda Tollinger, Martin Kwiatkowski, Marcel Müller, Thomas Anal Chem [Image: see text] Additive manufacturing (3D printing) has greatly revolutionized the way researchers approach certain technical challenges. Despite its outstanding print quality and resolution, stereolithography (SLA) printing is cost-effective and relatively accessible. However, applications involving mass spectrometry (MS) are few due to residual oligomers and additives leaching from SLA-printed devices that interfere with MS analyses. We identified the crosslinking agent urethane dimethacrylate as the main contaminant derived from SLA prints. A stringent washing and post-curing protocol mitigated sample contamination and rendered SLA prints suitable for MS hyphenation. Thereafter, SLA printing was used to produce 360 μm I.D. microcolumn chips with excellent structural properties. By packing the column with polystyrene microspheres and covalently immobilizing pepsin, an exceptionally effective microscale immobilized enzyme reactor (μIMER) was created. Implemented in an online liquid chromatography-MS/MS setup, the protease microcolumn enabled reproducible protein digestion and peptide mapping with 100% sequence coverage obtained for three different recombinant proteins. Additionally, when assessing the μIMER digestion efficiency for complex proteome samples, it delivered a 144-fold faster and significantly more efficient protein digestion compared to 24 h for bulk digestion. The 3D-printed μIMER withstands remarkably high pressures above 130 bar and retains its activity for several weeks. This versatile platform will enable researchers to produce tailored polymer-based enzyme reactors for various applications in analytical chemistry and beyond. American Chemical Society 2022-06-09 2022-06-21 /pmc/articles/PMC9218953/ /pubmed/35678765 http://dx.doi.org/10.1021/acs.analchem.1c05232 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Rainer, Tobias Egger, Anna-Sophia Zeindl, Ricarda Tollinger, Martin Kwiatkowski, Marcel Müller, Thomas 3D-Printed High-Pressure-Resistant Immobilized Enzyme Microreactor (μIMER) for Protein Analysis |
title | 3D-Printed High-Pressure-Resistant Immobilized Enzyme
Microreactor (μIMER) for Protein Analysis |
title_full | 3D-Printed High-Pressure-Resistant Immobilized Enzyme
Microreactor (μIMER) for Protein Analysis |
title_fullStr | 3D-Printed High-Pressure-Resistant Immobilized Enzyme
Microreactor (μIMER) for Protein Analysis |
title_full_unstemmed | 3D-Printed High-Pressure-Resistant Immobilized Enzyme
Microreactor (μIMER) for Protein Analysis |
title_short | 3D-Printed High-Pressure-Resistant Immobilized Enzyme
Microreactor (μIMER) for Protein Analysis |
title_sort | 3d-printed high-pressure-resistant immobilized enzyme
microreactor (μimer) for protein analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218953/ https://www.ncbi.nlm.nih.gov/pubmed/35678765 http://dx.doi.org/10.1021/acs.analchem.1c05232 |
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