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

Author:

Raykova DoroteyaORCID,Kermpatsou DespoinaORCID,Malmqvist TonyORCID,Harrison Philip J.,Sander Marie RubinORCID,Stiller ChristianeORCID,Heldin JohanORCID,Leino Mattias,Ricardo SaraORCID,Klemm AnnaORCID,David LeonorORCID,Spjuth OlaORCID,Vemuri KalyaniORCID,Dimberg AnnaORCID,Sundqvist Anders,Norlin MariaORCID,Klaesson Axel,Kampf Caroline,Söderberg OlaORCID

Abstract

AbstractDetermining 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.

Funder

Vetenskapsrådet

Cancerfonden

Stiftelsen för Strategisk Forskning

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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