Molecular constituents of the postsynaptic density fraction revealed by proteomic analysis using multidimensional liquid chromatography-tandem mass spectrometry

被引:168
作者
Yoshimura, Y
Yamauchi, Y
Shinkawa, T
Taoka, M
Donai, H
Takahashi, N
Isobe, T
Yamauchi, T
机构
[1] Univ Tokushima, Fac Pharmaceut Sci, Dept Biochem, Tokushima 7708505, Japan
[2] Tokyo Metropolitan Univ, Grad Sch Sci, Dept Chem, Hachioji, Tokyo, Japan
[3] Tokyo Univ Agr & Technol, Dept Appl Biol Sci, Tokyo, Japan
关键词
excitatory synapse; liquid chromatography; mass spectrometry; postsynaptic density; protein composition; proteomics;
D O I
10.1046/j.1471-4159.2003.02136.x
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
Protein constituents of the postsynaptic density (PSD) fraction were analysed using an integrated liquid chromatography (LC)-based protein identification system, which was constructed by coupling microscale two-dimensional liquid chromatography (2DLC) with electrospray ionization (ESI) tandem mass spectrometry (MS/MS) and an automated data analysis system. The PSD fraction prepared from rat forebrain was solubilized in 6 <smallcapitals>m</smallcapitals> guanidium hydrochloride, and the proteins were digested with trypsin after S-carbamoylmethylation under reducing conditions. The tryptic peptide mixture was then analysed with the 2DLC-MS/MS system in a data-dependent mode, and the resultant spectral data were automatically processed to search a genome sequence database for protein identification. In triplicate analyses, the system allowed assignments of 5264 peptides, which could finally be attributed to 492 proteins. The PSD contained various proteins involved in signalling transduction, including receptors, ion channel proteins, protein kinases and phosphatases, G-protein and related proteins, scaffold proteins, and adaptor proteins. Structural proteins, including membrane proteins involved in cell adhesion and cell-cell interaction, proteins involved in endocytosis, motor proteins, and cytoskeletal proteins were also abundant. These results provide basic data on a major protein set associated with the PSD and a basis for future functional studies of this important neural machinery.
引用
收藏
页码:759 / 768
页数:10
相关论文
共 40 条
[1]   MAMMALIAN HOMOLOGS OF CAENORHABDITIS-ELEGANS UNC-13 GENE DEFINE NOVEL FAMILY OF C-2-DOMAIN PROTEINS [J].
BROSE, N ;
HOFMANN, K ;
HATA, Y ;
SUDHOF, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :25273-25280
[2]   ISOLATION OF POSTSYNAPTIC DENSITIES FROM RAT-BRAIN [J].
COTMAN, CW ;
BANKER, G ;
CHURCHILL, L ;
TAYLOR, D .
JOURNAL OF CELL BIOLOGY, 1974, 63 (02) :441-455
[3]   Bassoon, a novel zinc-finger CAG/glutamine-repeat protein selectively localized at the active zone of presynaptic nerve terminals [J].
Dieck, ST ;
Sanmartí-Vila, L ;
Langnaese, K ;
Richter, K ;
Kindler, S ;
Soyke, A ;
Wex, H ;
Smalla, KH ;
Kämpf, U ;
Fränzer, JT ;
Stumm, M ;
Garner, CC ;
Gundelfinger, ED .
JOURNAL OF CELL BIOLOGY, 1998, 142 (02) :499-509
[4]   Dendritic and postsynaptic protein synthetic machinery [J].
Gardiol, A ;
Racca, C ;
Triller, A .
JOURNAL OF NEUROSCIENCE, 1999, 19 (01) :168-179
[5]   IDENTIFICATION OF THE MAJOR POSTSYNAPTIC DENSITY PROTEIN AS HOMOLOGOUS WITH THE MAJOR CALMODULIN-BINDING SUBUNIT OF A CALMODULIN-DEPENDENT PROTEIN-KINASE [J].
GOLDENRING, JR ;
MCGUIRE, JS ;
DELORENZO, RJ .
JOURNAL OF NEUROCHEMISTRY, 1984, 42 (04) :1077-1084
[7]  
Hu BR, 1998, J NEUROSCI, V18, P625
[8]   Proteomic analysis of NMDA receptor-adhesion protein signaling complexes [J].
Husi, H ;
Ward, MA ;
Choudhary, JS ;
Blackstock, WP ;
Grant, SGN .
NATURE NEUROSCIENCE, 2000, 3 (07) :661-669
[9]  
ISOBE T, 2003, PROTEINS PROTEOMICS, P869
[10]   Regulation and function of local protein synthesis in neuronal dendrites [J].
Jiang, CG ;
Schuman, EM .
TRENDS IN BIOCHEMICAL SCIENCES, 2002, 27 (10) :506-513