Detection of proteins sumoylated in vivo and in vitro.

Kevin D. Sarge, Ok Kyong Park-Sarge

Producción científica: Articlerevisión exhaustiva

31 Citas (Scopus)

Resumen

Small ubiquitin-related modifier (SUMO) is an ubiquitin-like protein that is covalently attached to a variety of target proteins. Unlike ubiquitination, sumoylation does not target proteins for proteolytic breakdown, but is instead involved in regulating multiple protein functional properties including protein-protein interactions and subcellular targeting, to name a few. Protein sumoylation has been particularly well characterized as a regulator of many nuclear processes as well as nuclear structure, making the characterization of this modification vital for understanding nuclear structure and function. Consequently, there has been intense interest in identifying new proteins that are targets of this modification and determining what role it plays in regulating their functions. This chapter presents methodologies for determining whether a particular protein is a substrate of sumoylation, and for identifying the lysine residue(s) where the modification occurs.

Idioma originalEnglish
Páginas (desde-hasta)265-277
Número de páginas13
PublicaciónMethods in Molecular Biology
Volumen590
DOI
EstadoPublished - 2009

Financiación

FinanciadoresNúmero del financiador
National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical SciencesR01GM064606

    ASJC Scopus subject areas

    • Molecular Biology
    • Genetics

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