posted on 2016-02-20, 20:41authored byKanae Yumimoto, Masaki Matsumoto, Koji Oyamada, Toshiro Moroishi, Keiichi I. Nakayama
Although elucidation of enzyme–substrate relations
is fundamental
to the advancement of biology, universal approaches to the identification
of substrates for a given enzyme have not been established. It is
especially difficult to identify substrates for ubiquitin ligases,
given that most such substrates are immediately ubiquitylated and
degraded as a result of their association with the enzyme. We here
describe the development of a new approach, DiPIUS (differential proteomics-based
identification of ubiquitylation substrates), to the discovery of
substrates for ubiquitin ligases. We applied DiPIUS to Fbxw7α,
Skp2, and Fbxl5, three of the most well-characterized F-box proteins,
and identified candidate substrates including previously known targets.
DiPIUS is thus a powerful tool for unbiased and comprehensive screening
for substrates of ubiquitin ligases.