학술논문

Protein microarray analysis identifies cyclic nucleotide phosphodiesterase as an interactor of Nogo-A.
Document Type
Article
Source
Neuropathology. Feb2010, Vol. 30 Issue 1, p7-14. 8p. 2 Color Photographs, 1 Diagram, 1 Chart.
Subject
*CYCLIC nucleotide phosphodiesterases
*NEURONS
*CENTRAL nervous system
*AMINO acids
*PROTEINS
Language
ISSN
0919-6544
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. [ABSTRACT FROM AUTHOR]