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Updated: Feb 5, 2026

Detection of Protein Ubiquitination
Published on: August 19, 2009
How to Target Viral and Bacterial Effector Proteins Interfering with Ubiquitin Signaling
Gerbrand J van der Heden van Noort1, Huib Ovaa2
1Department of Cell and Chemical Biology, Chemical Immunology, Oncode Institute, Leiden University Medical Centre, 2333 ZC, Leiden, The Netherlands. gvanderheden@lumc.nl.
Abstract:
Ubiquitination is a frequently occurring and very diverse posttranslational modification influencing a wide scope of cellular processes. Ubiquitin (Ub) has the unique ability to form eight different lysine-linked polymeric chains, mixed chains and engages with ubiquitin-like (Ubl) molecules. The distinct signals evoked by specific enzymes play a crucial role in, for instance, proteasome-mediated protein degradation, cell cycle regulation, and DNA damage responses. Due to the large variety of cellular functions that this posttranslational modification influences, the enzymes that construct such Ub modifications, and subsequently controle and degrade these signals, is enormous. In this chapter, we will discuss the current state-of-the-art of activity-based probes, reporter substrates, and other relevant tools based on Ub as recognition element, to study the enzymes involved in the complex system of ubiquitination.
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