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Generation of the UFM1 Toolkit for Profiling UFM1-Specific Proteases and Ligases.
Witting, Katharina F; van der Heden van Noort, Gerbrand J; Kofoed, Christian; Talavera Ormeño, Cami; El Atmioui, Dris; Mulder, Monique P C; Ovaa, Huib.
Afiliação
  • Witting KF; Oncode Institute & Department of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.
  • van der Heden van Noort GJ; Oncode Institute & Department of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.
  • Kofoed C; Department of Chemistry, Center for Evolutionary Chemical Biology, University of Copenhagen, Universitetsparken 5, 2100, Copenhagen, Denmark.
  • Talavera Ormeño C; Oncode Institute & Department of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.
  • El Atmioui D; Oncode Institute & Department of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.
  • Mulder MPC; Oncode Institute & Department of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.
  • Ovaa H; Oncode Institute & Department of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.
Angew Chem Int Ed Engl ; 57(43): 14164-14168, 2018 10 22.
Article em En | MEDLINE | ID: mdl-30188611
ABSTRACT
Ubiquitin-fold modifier 1 (UFM1) is a reversible post-translational modifier that is covalently attached to target proteins through an enzymatic cascade and removed by designated proteases. Abnormalities in this process, referred to as Ufmylation, have been associated with a variety of human diseases. Given this, the UFM1-specific enzymes represent potential therapeutic targets; however, understanding of their biological function has been hampered by the lack of chemical tools for activity profiling. To address this unmet need, a diversifiable platform for UFM1 activity-based probes (ABPs) utilizing a native chemical ligation (NCL) strategy was developed, enabling the generation of a variety of tools to profile both UFM1 conjugating and deconjugating enzymes. The use of the probes is demonstrated in vitro and in vivo for monitoring UFM1 enzyme reactivity, opening new research avenues.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeo Hidrolases / Sondas Moleculares / Proteínas / Processamento de Proteína Pós-Traducional Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeo Hidrolases / Sondas Moleculares / Proteínas / Processamento de Proteína Pós-Traducional Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article