Literature DB >> 16275322

High-throughput assay to monitor formation of the E2-ubiquitin thioester intermediate.

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.

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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


  1 in total

1.  Wheat germ-based protein libraries for the functional characterisation of the Arabidopsis E2 ubiquitin conjugating enzymes and the RING-type E3 ubiquitin ligase enzymes.

Authors:  Abdelaziz Ramadan; Keiichirou Nemoto; Motoaki Seki; Kazuo Shinozaki; Hiroyuki Takeda; Hirotaka Takahashi; Tatsuya Sawasaki
Journal:  BMC Plant Biol       Date:  2015-11-10       Impact factor: 4.215

  1 in total

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