Identification of brassinosteroid signaling complexes by coimmunoprecipitation and mass spectrometry

2Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A combination of coimmunoprecipitation (coIP) of tagged proteins followed by protein identification and quantitation using Liquid Chromatography Mass Spectrometry/Mass Spectrometry (LCMS/MS) has proven to be a reliable method to qualitatively characterize membrane-bound receptor complexes from plants. Success depends on a range of parameters, such as abundance and stability of the complex and functionality of the tagged receptors, efficiency of the protein complex isolation procedure, MS equipment, and analysis software in use. In this Chapter, we focus on the use of one of the green fluorescent protein-tagged receptors of the SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) family, of which SERK3, also known as BRASSINOSTEROID INSENSITIVE1 (BRI1) ASSOCIATED KINASE1 (BAK1), is a coreceptor of BRI1. Like BRI1 itself, SERK3 is a leucine-rich repeat receptor kinase (LRR RK) with a single-pass transmembrane domain. The latest updated laboratory protocol is presented as well as examples of data analysis and typical results obtained. Potential drawbacks of the procedure employed for plant membrane proteins will be pointed out.

Cite

CITATION STYLE

APA

van Dongen, W., van Heerde, L., Boeren, S., & de Vries, S. C. (2017). Identification of brassinosteroid signaling complexes by coimmunoprecipitation and mass spectrometry. In Methods in Molecular Biology (Vol. 1564, pp. 145–154). Humana Press Inc. https://doi.org/10.1007/978-1-4939-6813-8_12

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free