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Publication : Competition between Delta and the Abruptex domain of Notch.

First Author  Pei Zifei Year  2008
Journal  BMC Dev. Biol. Volume  8
Pages  4 PubMed ID  18208612
Abstract Text  Extracellular domains of the Notch family of signalling receptors contain many EGF repeat domains, as do their major ligands. Some EGF repeats are modified by O-fucosylation, and most have no identified role in ligand binding. Using a binding assay with purified proteins in vitro, it was determined that, in addition to binding to Delta, the ligand binding region of Notch bound to EGF repeats 22-27 of Notch, but not to other EGF repeat regions of Notch. EGF repeats 22-27 of Drosophila Notch overlap the genetically-defined 'Abruptex' region, and competed with Delta for binding to proteins containing the ligand-binding domain. Delta differed from the Abruptex domain in showing markedly enhanced binding at acid pH. Both Delta and the Abruptex region are heavily modified by protein O-fucosylation, but the split mutation of Drosophila Notch, which affects O-fucosylation of EGF repeat 14, did not affect binding of Notch to either Delta or the Abruptex region. The Abruptex region may serve as a barrier to Notch activation by competing for the ligand-binding domain of Notch. Doi  10.1186/1471-213X-8-4
Month  Jan

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