Literature DB >> 29091453

StUbEx PLUS-A Modified Stable Tagged Ubiquitin Exchange System for Peptide Level Purification and In-Depth Mapping of Ubiquitination Sites.

Vyacheslav Akimov1, Louise C B Olsen1, Sten V F Hansen1, Inigo Barrio-Hernandez1, Michele Puglia1, Søren S Jensen1, Ilia A Solov'yov1, Irina Kratchmarova1, Blagoy Blagoev1.   

Abstract

Modulation of protein activities by reversible post-translational modifications (PTMs) is a major molecular mechanism involved in the control of virtually all cellular processes. One of these PTMs is ubiquitination, which regulates key processes including protein degradation, cell cycle, DNA damage repair, and signal transduction. Because of its importance for numerous cellular functions, ubiquitination has become an intense topic of research in recent years, and proteomics tools have greatly facilitated the identification of many ubiquitination targets. Taking advantage of the StUbEx strategy for exchanging the endogenous ubiquitin with an epitope-tagged version, we created a modified system, StUbEx PLUS, which allows precise mapping of ubiquitination sites by mass spectrometry. Application of StUbEx PLUS to U2OS cells treated with proteasomal inhibitors resulted in the identification of 41 589 sites on 7762 proteins, which thereby revealed the ubiquitous nature of this PTM and demonstrated the utility of the approach for comprehensive ubiquitination studies at site-specific resolution.

Keywords:  LC−MS; N-terminal ubiquitination; mass spectrometry; on-bead digestion; proteasome; ubiquitin; ubiquitin chains; ubiquitination sites

Mesh:

Substances:

Year:  2017        PMID: 29091453     DOI: 10.1021/acs.jproteome.7b00566

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  11 in total

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Review 10.  Protein complexes and neighborhoods driving autophagy.

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