The Postsynaptic Density Proteins Homer and Shank Form a Polymeric Network Structure

被引:278
作者
Hayashi, Mariko Kato [1 ,2 ]
Tang, Chunyan [3 ]
Verpelli, Chiara [4 ,5 ]
Narayanan, Radhakrishnan [1 ]
Stearns, Marissa H. [1 ]
Xu, Rui-Ming [6 ,7 ]
Li, Huilin [3 ]
Sala, Carlo [4 ,5 ]
Hayashi, Yasunori [1 ,2 ]
机构
[1] MIT, Dept Brain & Cognit Sci, RIKEN MIT Neurosci Res Ctr, Picower Inst Learning & Memory, Cambridge, MA 02139 USA
[2] RIKEN, Brain Sci Inst, Wako, Saitama 3510198, Japan
[3] Brookhaven Natl Lab, Dept Biol, Upton, NY 11973 USA
[4] Univ Milan, Consiglio Nazl Ric, Inst Neurosci, I-20129 Milan, Italy
[5] Univ Milan, Dept Pharmacol, I-20129 Milan, Italy
[6] New York Univ, Structural Biol Program, Skirball Inst Biomol Med, Helen L & Martin S Kimmel Ctr Biol & Med,Sch Med, New York, NY 10016 USA
[7] New York Univ, Sch Med, Dept Pharmacol, New York, NY 10016 USA
关键词
CRYSTAL-STRUCTURE; COMPLEX REVEALS; RAT FOREBRAIN; EVH1; DOMAIN; KINASE-II; FAMILY; RECEPTOR; SYNAPSES; BINDS; RECOGNITION;
D O I
10.1016/j.cell.2009.01.050
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
The postsynaptic density (PSD) is crucial for synaptic functions, but the molecular architecture retaining its structure and components remains elusive. Homer and Shank are among the most abundant scaffolding proteins in the PSD, working synergistically for maturation of dendritic spines. Here, we demonstrate that Homer and Shank, together, form a mesh-like matrix structure. Crystallographic analysis of this region revealed a pair of parallel dimeric coiled coils intercalated in a tail-to-tail fashion to form a tetramer, giving rise to the unique configuration of a pair of N-terminal EVH1 domains at each end of the coiled coil. In neurons, the tetramerization is required for structural integrity of the dendritic spines and recruitment of proteins to synapses. We propose that the Homer-Shank complex serves as a structural framework and as an assembly platform for other PSD proteins.
引用
收藏
页码:159 / 171
页数:13
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