Biochemical analysis of protein SUMOylation.

Curr Protoc Mol Biol

Department of Molecular Medicine, Beckman Research Institute of the City of Hope, Duarte, California, USA.

Published: July 2012

SUMOylation, the covalent attachment of Small Ubiquitin-like MOdifier (SUMO) polypeptides to other proteins, is among the most important post-translational modifications that regulate the functional properties of a large number of proteins. SUMOylation is broadly involved in cellular processes such as gene transcription, hormone response, signal transduction, DNA repair, and nuclear transport. SUMO modification has also been implicated in the pathogenesis of human diseases, such as cancer, neurodegenerative disorders, and viral infection. Attachment of a SUMO protein to another protein is carried out in multiple steps catalyzed by three enzymes. This unit describes and discusses the in vitro biochemical methods used for investigating each step of the SUMOylation process. In addition, a high-throughput screening protocol is included for the identification of inhibitors of SUMOylation.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3477621PMC
http://dx.doi.org/10.1002/0471142727.mb1029s99DOI Listing

Publication Analysis

Top Keywords

sumoylation
5
biochemical analysis
4
analysis protein
4
protein sumoylation
4
sumoylation sumoylation
4
sumoylation covalent
4
covalent attachment
4
attachment small
4
small ubiquitin-like
4
ubiquitin-like modifier
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!