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Studying Protein Ubiquitylation in Yeast.

Research paper by Junie J Hovsepian, Michel M Becuwe, Oded O Kleifeld, Michael H MH Glickman, Sébastien S Léon

Indexed on: 11 Sep '16Published on: 11 Sep '16Published in: Methods in molecular biology (Clifton, N.J.)



Abstract

Ubiquitylation is a reversible posttranslational modification that is critical for most, if not all, cellular processes and essential for viability. Ubiquitin conjugates to substrate proteins either as a single moiety (monoubiquitylation) or as polymers composed of ubiquitin molecules linked to each other with various topologies and structures (polyubiquitylation). This contributes to an elaborate ubiquitin code that is decrypted by specific ubiquitin-binding proteins. Indeed, these different types of ubiquitylation have different functional outcomes, notably affecting the stability of the substrate, its interactions, its activity, or its subcellular localization. In this chapter, we describe protocols to determine whether a protein is ubiquitylated, to identify the site that is ubiquitylated, and provide direction to study the topology of the ubiquitin modification, in the yeast Saccharomyces cerevisiae.