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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...

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Autores principales: Petell, Christopher J, Randene, Kathyrn, Pappas, Michael, Sandoval, Diego, Strahl, Brian D, Harrison, Joseph S, Steimel, Joshua P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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