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蛋白质微阵列分析鉴定出环核苷酸磷酸二酯酶为 Nogo-A 的相互作用蛋白。

Protein microarray analysis identifies cyclic nucleotide phosphodiesterase as an interactor of Nogo-A.

机构信息

Department of Bioinformatics and Molecular Neuropathology, Meiji Pharmaceutical University, Tokyo 204-8588, Japan.

出版信息

Neuropathology. 2010 Feb 1;30(1):7-14. doi: 10.1111/j.1440-1789.2009.01035.x. Epub 2009 Jun 7.

Abstract

Nogo-A, a neurite outgrowth inhibitor, is expressed exclusively on oligodendrocytes and neurons in the CNS. The central domain of Amino-Nogo spanning amino acids 567-748 in the human Nogo-A designated NIG, mediates persistent inhibition of axonal outgrowth and induces growth cone collapse by signaling through an as yet unidentified NIG receptor. We identified 82 NIG-interacting proteins by screening a high-density human protein microarray composed of 5000 proteins with a recombinant NIG protein as a probe. Following an intensive database search, we selected 12 neuron/oligodendrocyte-associated NIG interactors. Among them, we verified the molecular interaction of NIG with 2', 3'-cyclic nucleotide 3'-phosphodiesterase (CNP), a cell type-specific marker of oligodendrocytes, by immunoprecipitation and cell imaging analysis. Although CNP located chiefly in the cytoplasm of oligodendrocytes might not serve as a cell-surface NIG receptor, it could act as a conformational stabilizer for the intrinsically unstructured large segment of Amino-Nogo.

摘要

Nogo-A 是一种神经突生长抑制剂,仅在中枢神经系统的少突胶质细胞和神经元中表达。Nogo-A 中氨基酸 567-748 所示的中央结构域(amino-Nogo,命名为 NIG)介导轴突生长的持续抑制,并通过尚未鉴定的 NIG 受体信号诱导生长锥塌陷。我们通过用重组 NIG 蛋白作为探针筛选由 5000 种蛋白质组成的高密度人蛋白质微阵列,鉴定了 82 种 NIG 相互作用蛋白。经过密集的数据库搜索,我们选择了 12 种神经元/少突胶质细胞相关的 NIG 相互作用蛋白。其中,我们通过免疫沉淀和细胞成像分析验证了 NIG 与 2',3'-环核苷酸 3'-磷酸二酯酶(CNP)的分子相互作用,CNP 是少突胶质细胞的细胞类型特异性标志物。尽管主要位于少突胶质细胞质中的 CNP 可能不作为细胞表面的 NIG 受体,但它可以作为氨基酸 Nogo 大无规则结构域的构象稳定剂。

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