Hayashi Mariko Kato, Tang Chunyan, Verpelli Chiara, Narayanan Radhakrishnan, Stearns Marissa H, Xu Rui-Ming, Li Huilin, Sala Carlo, Hayashi Yasunori
RIKEN-MIT Neuroscience Research Center, The Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Cell. 2009 Apr 3;137(1):159-71. doi: 10.1016/j.cell.2009.01.050.
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.
突触后致密区(PSD)对突触功能至关重要,但其维持结构和组分的分子架构仍不清楚。Homer和Shank是PSD中最丰富的支架蛋白,协同作用促进树突棘成熟。在此,我们证明Homer和Shank共同形成一种网状基质结构。该区域的晶体学分析显示,一对平行的二聚体卷曲螺旋以尾对尾方式插入形成四聚体,在卷曲螺旋两端产生一对独特的N端EVH1结构域构型。在神经元中,四聚化对于树突棘的结构完整性以及蛋白质向突触的募集是必需的。我们提出,Homer-Shank复合体作为一种结构框架以及其他PSD蛋白的组装平台。