Structure of the HECT:ubiquitin complex and its role in ubiquitin chain elongation

被引:138
作者
Maspero, Elena [2 ]
Mari, Sara [2 ]
Valentini, Eleonora [2 ]
Musacchio, Andrea [1 ]
Fish, Alexander [3 ]
Pasqualato, Sebastiano [1 ,4 ]
Polo, Simona [2 ,5 ]
机构
[1] Ist Europeo Oncol, Dipartimento Oncol Sperimentale, I-20139 Milan, Italy
[2] Fdn Ist FIRC Oncol Mol, IFOM, I-20139 Milan, Italy
[3] Netherlands Canc Inst, Div Biochem, NL-1066 CX Amsterdam, Netherlands
[4] Cogentech Consortium Genom Technol, Crystallog Unit, I-20139 Milan, Italy
[5] Univ Milan, Dipartimento Med Chirurg & Odontoiatria, I-20122 Milan, Italy
关键词
catalysis; E3; ligase; polyubiquitination; structure; ubiquitin; BINDING; LIGASE; DETERMINANTS; MECHANISM; INSIGHTS; E3S;
D O I
10.1038/embor.2011.21
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several mechanisms have been proposed for the synthesis of substrate-linked ubiquitin chains. HECT ligases directly catalyse protein ubiquitination and have been found to non-covalently interact with ubiquitin. We report crystal structures of the Nedd4 HECT domain, alone and in complex with ubiquitin, which show a new binding mode involving two surfaces on ubiquitin and both subdomains of the HECT N-lobe. The structures suggest a model for HECT-to-substrate ubiquitin transfer, in which the growing chain on the substrate is kept close to the catalytic cysteine to promote processivity. Mutational analysis highlights differences between the processes of substrate polyubiquitination and self-ubiquitination.
引用
收藏
页码:342 / 349
页数:8
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