Literature DB >> 34458413

In vitro Ubiquitin Dimer Formation Assay.

Sheng Wang1, Ling Cao1,2, Hong Wang1.   

Abstract

The process of protein ubiquitination typically consists of three sequential steps to add an ubiquitin (Ub) or Ub chain to a substrate protein, requiring three different enzymes, ubiquitin activating enzyme (E1), ubiquitin conjugating enzyme (E2), and ubiquitin protein ligase (E3). Most E2s possess the classical E2 activity in forming E2-Ub complex through a thioester linkage, in presence of an E1 and Ub. Additionally, some E2s have the ability of catalyzing the formation of free Ub dimer. Such activity indicates an important role of these E2s in ubiquitination pathway. Thus, we developed an in vitro Ub dimer formation assay to determine the activity of certain E2s. Moreover, by using Ub mutants, in which different lysine residues are mutated, the specific linkage of dimer can also be determined.
Copyright © 2017 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Arabidopsis UBC22 ; E2; K11 linkage; Ubiquitin dimer formation; Ubiquitination

Year:  2017        PMID: 34458413      PMCID: PMC8376499          DOI: 10.21769/BioProtoc.2082

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  1 in total

1.  Arabidopsis ubiquitin-conjugating enzyme UBC22 is required for female gametophyte development and likely involved in Lys11-linked ubiquitination.

Authors:  Sheng Wang; Ling Cao; Hong Wang
Journal:  J Exp Bot       Date:  2016-04-10       Impact factor: 6.992

  1 in total

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