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A method for Boolean analysis of protein interactions at a molecular level

Determining the levels of protein–protein interactions is essential for the analysis of signaling within the cell, characterization of mutation effects, protein function and activation in health and disease, among others. Herein, we describe MolBoolean – a method to detect interactions between endog...

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Autores principales: Raykova, Doroteya, Kermpatsou, Despoina, Malmqvist, Tony, Harrison, Philip J., Sander, Marie Rubin, Stiller, Christiane, Heldin, Johan, Leino, Mattias, Ricardo, Sara, Klemm, Anna, David, Leonor, Spjuth, Ola, Vemuri, Kalyani, Dimberg, Anna, Sundqvist, Anders, Norlin, Maria, Klaesson, Axel, Kampf, Caroline, Söderberg, Ola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375095/
https://www.ncbi.nlm.nih.gov/pubmed/35963857
http://dx.doi.org/10.1038/s41467-022-32395-w
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author Raykova, Doroteya
Kermpatsou, Despoina
Malmqvist, Tony
Harrison, Philip J.
Sander, Marie Rubin
Stiller, Christiane
Heldin, Johan
Leino, Mattias
Ricardo, Sara
Klemm, Anna
David, Leonor
Spjuth, Ola
Vemuri, Kalyani
Dimberg, Anna
Sundqvist, Anders
Norlin, Maria
Klaesson, Axel
Kampf, Caroline
Söderberg, Ola
author_facet Raykova, Doroteya
Kermpatsou, Despoina
Malmqvist, Tony
Harrison, Philip J.
Sander, Marie Rubin
Stiller, Christiane
Heldin, Johan
Leino, Mattias
Ricardo, Sara
Klemm, Anna
David, Leonor
Spjuth, Ola
Vemuri, Kalyani
Dimberg, Anna
Sundqvist, Anders
Norlin, Maria
Klaesson, Axel
Kampf, Caroline
Söderberg, Ola
author_sort Raykova, Doroteya
collection PubMed
description Determining the levels of protein–protein interactions is essential for the analysis of signaling within the cell, characterization of mutation effects, protein function and activation in health and disease, among others. Herein, we describe MolBoolean – a method to detect interactions between endogenous proteins in various subcellular compartments, utilizing antibody-DNA conjugates for identification and signal amplification. In contrast to proximity ligation assays, MolBoolean simultaneously indicates the relative abundances of protein A and B not interacting with each other, as well as the pool of A and B proteins that are proximal enough to be considered an AB complex. MolBoolean is applicable both in fixed cells and tissue sections. The specific and quantifiable data that the method generates provide opportunities for both diagnostic use and medical research.
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spelling pubmed-93750952022-08-15 A method for Boolean analysis of protein interactions at a molecular level Raykova, Doroteya Kermpatsou, Despoina Malmqvist, Tony Harrison, Philip J. Sander, Marie Rubin Stiller, Christiane Heldin, Johan Leino, Mattias Ricardo, Sara Klemm, Anna David, Leonor Spjuth, Ola Vemuri, Kalyani Dimberg, Anna Sundqvist, Anders Norlin, Maria Klaesson, Axel Kampf, Caroline Söderberg, Ola Nat Commun Article Determining the levels of protein–protein interactions is essential for the analysis of signaling within the cell, characterization of mutation effects, protein function and activation in health and disease, among others. Herein, we describe MolBoolean – a method to detect interactions between endogenous proteins in various subcellular compartments, utilizing antibody-DNA conjugates for identification and signal amplification. In contrast to proximity ligation assays, MolBoolean simultaneously indicates the relative abundances of protein A and B not interacting with each other, as well as the pool of A and B proteins that are proximal enough to be considered an AB complex. MolBoolean is applicable both in fixed cells and tissue sections. The specific and quantifiable data that the method generates provide opportunities for both diagnostic use and medical research. Nature Publishing Group UK 2022-08-13 /pmc/articles/PMC9375095/ /pubmed/35963857 http://dx.doi.org/10.1038/s41467-022-32395-w Text en © The Author(s) 2022, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Raykova, Doroteya
Kermpatsou, Despoina
Malmqvist, Tony
Harrison, Philip J.
Sander, Marie Rubin
Stiller, Christiane
Heldin, Johan
Leino, Mattias
Ricardo, Sara
Klemm, Anna
David, Leonor
Spjuth, Ola
Vemuri, Kalyani
Dimberg, Anna
Sundqvist, Anders
Norlin, Maria
Klaesson, Axel
Kampf, Caroline
Söderberg, Ola
A method for Boolean analysis of protein interactions at a molecular level
title A method for Boolean analysis of protein interactions at a molecular level
title_full A method for Boolean analysis of protein interactions at a molecular level
title_fullStr A method for Boolean analysis of protein interactions at a molecular level
title_full_unstemmed A method for Boolean analysis of protein interactions at a molecular level
title_short A method for Boolean analysis of protein interactions at a molecular level
title_sort method for boolean analysis of protein interactions at a molecular level
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375095/
https://www.ncbi.nlm.nih.gov/pubmed/35963857
http://dx.doi.org/10.1038/s41467-022-32395-w
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