Literature DB >> 34432246

Global Mass Spectrometry-Based Analysis of Protein Ubiquitination Using K-ε-GG Remnant Antibody Enrichment.

Alissa J Nelson1, Yiying Zhu1, Jian Min Ren1, Matthew P Stokes2.   

Abstract

Ubiquitination is a post-translational modification that affects protein degradation as well as a variety of cellular processes. Methods that globally profile ubiquitination are powerful tools to better understand these processes. Here we describe an updated method for identification and quantification of thousands of sites of ubiquitination from cells, tissues, or other biological materials. The method involves cell lysis and digestion to peptides, immunoaffinity enrichment with an antibody recognizing di-glycine remnants left behind at ubiquitinated lysines, and liquid chromatography-tandem mass spectrometry analysis of the enriched peptides.
© 2021. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  LC-MS/MS; Mass spectrometry; PTMScan; Post-translational modification; Protein degradation; Proteomics; Ubiquitin; Ubiquitination

Mesh:

Substances:

Year:  2021        PMID: 34432246     DOI: 10.1007/978-1-0716-1665-9_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

Review 1.  Ubiquitin chain diversity at a glance.

Authors:  Masato Akutsu; Ivan Dikic; Anja Bremm
Journal:  J Cell Sci       Date:  2016-02-15       Impact factor: 5.285

Review 2.  Protein ubiquitination: a regulatory post-translational modification.

Authors:  K D Wilkinson
Journal:  Anticancer Drug Des       Date:  1987-10
  2 in total
  1 in total

Review 1.  Insights Into the Biogenesis and Emerging Functions of Lipid Droplets From Unbiased Molecular Profiling Approaches.

Authors:  Miguel Sánchez-Álvarez; Miguel Ángel Del Pozo; Marta Bosch; Albert Pol
Journal:  Front Cell Dev Biol       Date:  2022-06-08
  1 in total

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