CRL (Cullin-RING ubiquitin ligase) is the major class of plant E3 ubiquitin ligases. Immunoprecipitation-based methods are useful techniques for revealing interactions among Cullin-RING Ligase (CRL) subunits or between CRLs and other proteins, as well as for detecting poly-ubiquitin modifications of the CRLs themselves. Here, we describe two immunoprecipitation (IP) procedures suitable for CRLs in Arabidopsis: a procedure for IP analysis of CRL subunits and their interactors and a second procedure for in vivo ubiquitination analysis of the CRLs. Both protocols can be divided into two major steps: (1) preparation of cell extracts without disruption of protein interactions and (2) affinity purification of the protein complexes and subsequent detection. We provide a thorough description of all the steps, as well as advice on how to choose proper buffers for these analyses. We also suggest a series of negative controls that can be used to verify the specificity of the procedure.

Immunoprecipitation of Cullin-RING Ligases (CRLs) in Arabidopsis thaliana Seedlings / Franciosini, Anna; Serino, Giovanna. - STAMPA. - 1450(2016), pp. 11-21. - METHODS IN MOLECULAR BIOLOGY. [10.1007/978-1-4939-3759-2_2].

Immunoprecipitation of Cullin-RING Ligases (CRLs) in Arabidopsis thaliana Seedlings

SERINO, Giovanna
Ultimo
Writing – Original Draft Preparation
2016

Abstract

CRL (Cullin-RING ubiquitin ligase) is the major class of plant E3 ubiquitin ligases. Immunoprecipitation-based methods are useful techniques for revealing interactions among Cullin-RING Ligase (CRL) subunits or between CRLs and other proteins, as well as for detecting poly-ubiquitin modifications of the CRLs themselves. Here, we describe two immunoprecipitation (IP) procedures suitable for CRLs in Arabidopsis: a procedure for IP analysis of CRL subunits and their interactors and a second procedure for in vivo ubiquitination analysis of the CRLs. Both protocols can be divided into two major steps: (1) preparation of cell extracts without disruption of protein interactions and (2) affinity purification of the protein complexes and subsequent detection. We provide a thorough description of all the steps, as well as advice on how to choose proper buffers for these analyses. We also suggest a series of negative controls that can be used to verify the specificity of the procedure.
2016
Plant Proteostasis. Methods and Protocols
978-1-4939-3759-2
978-1-4939-3757-8
protein immunoprecipitation; protocol; ubiquitin ligase; ubiquitin; arabidopsis thaliana; plant
02 Pubblicazione su volume::02a Capitolo o Articolo
Immunoprecipitation of Cullin-RING Ligases (CRLs) in Arabidopsis thaliana Seedlings / Franciosini, Anna; Serino, Giovanna. - STAMPA. - 1450(2016), pp. 11-21. - METHODS IN MOLECULAR BIOLOGY. [10.1007/978-1-4939-3759-2_2].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/958083
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