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Global Mass Spectrometry-Based Analysis of Protein Ubiquitination Using K-ε-GG Remnant Antibody Enrichment.
Nelson, Alissa J; Zhu, Yiying; Ren, Jian Min; Stokes, Matthew P.
  • Nelson AJ; Cell Signaling Technology, INC, Danvers, MA, USA.
  • Zhu Y; Cell Signaling Technology, INC, Danvers, MA, USA.
  • Ren JM; Cell Signaling Technology, INC, Danvers, MA, USA.
  • Stokes MP; Cell Signaling Technology, INC, Danvers, MA, USA. mstokes@cellsignal.com.
Methods Mol Biol ; 2365: 203-216, 2021.
Article en En | MEDLINE | ID: mdl-34432246
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espectrometría de Masas Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espectrometría de Masas Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article