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Mechanically transduced immunosorbent assay to measure protein-protein interactions
Measuring protein-protein interaction (PPI) affinities is fundamental to biochemistry. Yet, conventional methods rely upon the law of mass action and cannot measure many PPIs due to a scarcity of reagents and limitations in the measurable affinity ranges. Here, we present a novel technique that leve...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479797/ https://www.ncbi.nlm.nih.gov/pubmed/34581668 http://dx.doi.org/10.7554/eLife.67525 |
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author | Petell, Christopher J Randene, Kathyrn Pappas, Michael Sandoval, Diego Strahl, Brian D Harrison, Joseph S Steimel, Joshua P |
author_facet | Petell, Christopher J Randene, Kathyrn Pappas, Michael Sandoval, Diego Strahl, Brian D Harrison, Joseph S Steimel, Joshua P |
author_sort | Petell, Christopher J |
collection | PubMed |
description | Measuring protein-protein interaction (PPI) affinities is fundamental to biochemistry. Yet, conventional methods rely upon the law of mass action and cannot measure many PPIs due to a scarcity of reagents and limitations in the measurable affinity ranges. Here, we present a novel technique that leverages the fundamental concept of friction to produce a mechanical signal that correlates to binding potential. The mechanically transduced immunosorbent (METRIS) assay utilizes rolling magnetic probes to measure PPI interaction affinities. METRIS measures the translational displacement of protein-coated particles on a protein-functionalized substrate. The translational displacement scales with the effective friction induced by a PPI, thus producing a mechanical signal when a binding event occurs. The METRIS assay uses as little as 20 pmols of reagents to measure a wide range of affinities while exhibiting a high resolution and sensitivity. We use METRIS to measure several PPIs that were previously inaccessible using traditional methods, providing new insights into epigenetic recognition. |
format | Online Article Text |
id | pubmed-8479797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84797972021-09-30 Mechanically transduced immunosorbent assay to measure protein-protein interactions Petell, Christopher J Randene, Kathyrn Pappas, Michael Sandoval, Diego Strahl, Brian D Harrison, Joseph S Steimel, Joshua P eLife Biochemistry and Chemical Biology Measuring protein-protein interaction (PPI) affinities is fundamental to biochemistry. Yet, conventional methods rely upon the law of mass action and cannot measure many PPIs due to a scarcity of reagents and limitations in the measurable affinity ranges. Here, we present a novel technique that leverages the fundamental concept of friction to produce a mechanical signal that correlates to binding potential. The mechanically transduced immunosorbent (METRIS) assay utilizes rolling magnetic probes to measure PPI interaction affinities. METRIS measures the translational displacement of protein-coated particles on a protein-functionalized substrate. The translational displacement scales with the effective friction induced by a PPI, thus producing a mechanical signal when a binding event occurs. The METRIS assay uses as little as 20 pmols of reagents to measure a wide range of affinities while exhibiting a high resolution and sensitivity. We use METRIS to measure several PPIs that were previously inaccessible using traditional methods, providing new insights into epigenetic recognition. eLife Sciences Publications, Ltd 2021-09-28 /pmc/articles/PMC8479797/ /pubmed/34581668 http://dx.doi.org/10.7554/eLife.67525 Text en © 2021, Petell et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Petell, Christopher J Randene, Kathyrn Pappas, Michael Sandoval, Diego Strahl, Brian D Harrison, Joseph S Steimel, Joshua P Mechanically transduced immunosorbent assay to measure protein-protein interactions |
title | Mechanically transduced immunosorbent assay to measure protein-protein interactions |
title_full | Mechanically transduced immunosorbent assay to measure protein-protein interactions |
title_fullStr | Mechanically transduced immunosorbent assay to measure protein-protein interactions |
title_full_unstemmed | Mechanically transduced immunosorbent assay to measure protein-protein interactions |
title_short | Mechanically transduced immunosorbent assay to measure protein-protein interactions |
title_sort | mechanically transduced immunosorbent assay to measure protein-protein interactions |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479797/ https://www.ncbi.nlm.nih.gov/pubmed/34581668 http://dx.doi.org/10.7554/eLife.67525 |
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