Lim S, Sala C, Yoon J, Park S, Kuroda S, Sheng M, Kim E
Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Yusong-ku, Daejon, 305-701, Korea.
Mol Cell Neurosci. 2001 Feb;17(2):385-97. doi: 10.1006/mcne.2000.0940.
The Shank family of proteins (also termed CortBP, ProSAP, or Synamon) is highly enriched in the postsynaptic density (PSD) of excitatory synapses in brain. Shank contains multiple domains for protein-protein interactions, including ankyrin repeats, SH3 domain, PDZ domain, SAM domain, and an extensive proline-rich region. We have identified a novel protein, termed Sharpin, that directly interacts with the ankyrin repeats of Shank. Sharpin is enriched in the PSD and forms a complex with Shank in heterologous cells and brain. Immunostaining reveals the presence of Sharpin at excitatory synapses and its colocalization with Shank. While the C-terminal half of Sharpin interacts with Shank, the N-terminal half of Sharpin mediates homomultimerization. Considering the fact that the ankyrin repeats and the SH3 domain of Shank can be truncated by alternative splicing, these results define Sharpin as a novel PSD protein that may regulate the complexity of the Shank-based protein network in an alternative splicing-dependent manner.
尚克蛋白家族(也称为CortBP、ProSAP或Synamon)在大脑兴奋性突触的突触后致密区(PSD)中高度富集。尚克蛋白包含多个用于蛋白质-蛋白质相互作用的结构域,包括锚蛋白重复序列、SH3结构域、PDZ结构域、SAM结构域以及一个广泛的富含脯氨酸的区域。我们鉴定出一种名为夏普林的新型蛋白质,它直接与尚克蛋白的锚蛋白重复序列相互作用。夏普林在PSD中富集,并在异源细胞和大脑中与尚克蛋白形成复合物。免疫染色显示夏普林存在于兴奋性突触处,并与尚克蛋白共定位。虽然夏普林的C端一半与尚克蛋白相互作用,但其N端一半介导同源多聚化。鉴于尚克蛋白的锚蛋白重复序列和SH3结构域可通过可变剪接被截断,这些结果将夏普林定义为一种新型的PSD蛋白,它可能以可变剪接依赖的方式调节基于尚克蛋白的蛋白质网络的复杂性。