An Optimized Single-Molecule Pull-Down Assay for Quantification of Protein Phosphorylation

Authors

Elizabeth M. Bailey, Department of Pathology, University of New Mexico School of Medicine
Emanuel Salazar-Cavazos, Department of Pathology, University of New Mexico School of Medicine
Rachel M. Grattan, Department of Pathology, University of New Mexico School of Medicine
Michael J. Wester, Department of Physics and Astronomy, University of New Mexico
David J. Schodt, Department of Physics and Astronomy, University of New Mexico
Julian A. Rojo, Department of Pathology, University of New Mexico School of Medicine
Keith A. Lidke, Department of Physics and Astronomy, University of New Mexico; Comprehensive Cancer Center, University of New Mexico Health Sciences Center
Diane S. Lidke, Department of Pathology, University of New Mexico School of Medicine; Comprehensive Cancer Center, University of New Mexico Health Sciences Center; dlidke@salud.unm.edu

Document Type

Article

Publication Date

6-6-2022

Abstract

Phosphorylation is a necessary posttranslational modification that regulates protein function and directs cell signaling outcomes. Current methods to measure protein phosphorylation cannot preserve the heterogeneity in phosphorylation across individual proteins. The single-molecule pull-down (SiMPull) assay was developed to investigate the composition of macromolecular complexes via immunoprecipitation of proteins on a glass coverslip followed by single-molecule imaging. The current technique is an adaptation of SiMPull that provides robust quantification of the phosphorylation state of full-length membrane receptors at the single-molecule level. Imaging thousands of individual receptors in this way allows for quantifying protein phosphorylation patterns. The present protocol details the optimized SiMPull procedure, from sample preparation to imaging. Optimization of glass preparation and antibody fixation protocols further enhances data quality. The current protocol provides code for the single-molecule data analysis that calculates the fraction of receptors phosphorylated within a sample. While this work focuses on phosphorylation of the epidermal growth factor receptor (EGFR), the protocol can be generalized to other membrane receptors and cytosolic signaling molecules.

Recommended Citation

Bailey EM, Salazar-Cavazos E, Grattan RM, Wester MJ, Schodt DJ, Rojo JA, Lidke KA, Lidke DS. An Optimized Single-Molecule Pull-Down Assay for Quantification of Protein Phosphorylation. J Vis Exp. 2022 Jun 6;(184):10.3791/63665. doi: 10.3791/63665. PMID: 35723488; PMCID: PMC9317552.