| Literature DB >> 16275322 |
Patrick Hauser1, Francesco Hofmann.
Abstract
Targeting components of ubiquitination pathways for drug discovery necessitates the development of high-capacity assays that monitor the ubiquitination process at defined steps of the E1-E2-E3 cascade. This chapter describes the development of an assay based on time-resolved fluorescence to monitor formation of the thioester intermediate between ubiquitin-conjugating enzymes (E2s) and ubiquitin. The methodology is exemplified by an assay tailored for the ubiquitin-conjugating enzyme Cdc34. This assay setup can be easily adapted to other E2s and is suitable to screen small molecule inhibitors of E2-thioester formation in a high-throughput mode.Entities:
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Year: 2005 PMID: 16275322 DOI: 10.1016/S0076-6879(05)98009-9
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600