Modifications and Targeting of Protein Termini Part A
Academic Press Inc (Verlag)
978-0-443-15772-1 (ISBN)
Additional sections cover Monitoring the interactions between N-degrons and N-recognins of the Arg/N-degron pathway, Characterization and chemical modulation of p62/SQSTM1 as an autophagic N-recognin of the Arg/N-degron pathway, Analysis of higher plant N-degron pathway components and substrates via expression in S. cerevisiae, and so much more.
Professor Thomas Arnesen received his Ph.D. in molecular biology from the University of Bergen, Norway in 2006. After postdoctoral work at Haukeland University Hospital and University of Rochester Medical Center, he established his own lab at the University of Bergen in 2010. His main interest has been protein N-terminal acetylation and the responsible enzymes, the N-terminal acetyltransferases (NATs). Using Saccharomyces cerevisiae and human cell models combined with in vitro approaches his lab and collaborators have i) identified and defined the presumed complete cytosolic human NAT-machinery including NATs acting post-translationally, ii) quantitatively analysed the N-terminal acetylomes of yeast and human cells, iii) developed novel assays for NAT-profiling, iv) gained mechanistic insights of the molecular and cellular effects of N-terminal acetylation, v) contributed to the understanding of the physiological and clinical importance of NATs by revealing the links between NatA and cancer cell survival and drug sensitisation, and lately by defining genetic disorders caused by pathogenic NAT variants. The Arnesen lab also contributed to solving the first NAT-structures and developing the first potent NAT-inhibitors. With Fred Sherman and Bogdan Polevoda, Arnesen introduced the NAA (N-alpha acetyltransferase) nomenclature of the N-terminal acetyltransferase genes and proteins, and he acts as the specialist advisor for the HUGO Gene Nomenclature Committee for these genes. Arnesen is one of the founders and council members of the International Society of Protein Termini (ISPT). He has organized several symposia on N-terminal acetylation, and in 2022 he was the head organizer of the EMBO Workshop ‘Protein Termini – From mechanism to biological impact’ in Bergen, Norway. Arnesen has co-authored more than 100 peer-reviewed publications. Today he is head of the Translational Cell Signaling and Metabolism group at the Dept. of Biomedicine, UiB, supported by the Research Council of Norway and ERC. Here his team continues the basic and translational research to understand the impact of protein N-terminal modifications.
1. Selective ribosome profiling as a tool to study interactions of translating ribosomes in mammalian cells Bernd Bukau, Jiri Koubek, Manuel Günnigmann and Günter Kramer 2. Deformylation of nascent chains on the ribosome Marina V. Rodnina, Lena Bögeholz, Evan Mercier and Wolfgang Wintermeyer 3. Optimizing purification and activity assays of N-terminal methyltransferase complexes Christine Schaner Tooley, Haley Parker and John Tooley 4. Site-specific a-N-terminal methylation on peptides through chemical and enzymatic methods Rong Huang and Ying Meng 5. Biochemical and structural analysis of N-myristoyltransferase-mediated protein tagging Thierry Meinnel, Carmela Giglione, Paul Monassa, Frédéric Rivière, Cyril Dian and Frédéric Frottin 6. Kinetic and catalytic features of N-myristoyltransferases Thierry Meinnel and Carmela Giglione 7. Detecting N-terminal myristoylation using metabolic Alk12 labeling Hening Lin and Yilai Xu 8. Peptide CoA conjugates for in situ proteomics profiling of acetyltransferase activities Iris Finkemeier, Jürgen Eirich, Julia Sindlinger, Stefan Schön and Dirk Schwarzer 9. A decoupled Virotrap approach to study the interactomes of N-terminal proteoforms Kris Gevaert, Annelies Bogaert, Tessa Van de Steene, Marnik Vuylsteke and Sven Eyckerman 10. The amino-dipeptidyl peptidases DPP8 and DPP9: purification, interaction studies and enzymatic assays Ruth Geiss-Friedlander, Laura Donzelli and Oguz Bolgi
| Erscheinungsdatum | 10.07.2023 |
|---|---|
| Reihe/Serie | Methods in Enzymology |
| Verlagsort | San Diego |
| Sprache | englisch |
| Maße | 152 x 229 mm |
| Gewicht | 450 g |
| Themenwelt | Naturwissenschaften ► Biologie ► Biochemie |
| Naturwissenschaften ► Biologie ► Genetik / Molekularbiologie | |
| ISBN-10 | 0-443-15772-3 / 0443157723 |
| ISBN-13 | 978-0-443-15772-1 / 9780443157721 |
| Zustand | Neuware |
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