Mammalian plasma membrane proteomics

被引:111
作者
Josic, Djuro
Clifton, James G.
机构
[1] Rhode Isl Hosp, COBRE Ctr Canc Res Dev, Providence, RI 02903 USA
[2] Brown Med Sch, Dept Med, Providence, RI USA
关键词
membrane domains; plasma membrane proteomics;
D O I
10.1002/pmic.200700139
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Plasma membrane proteins serve essential functions for cells, interacting with both cellular and extracellular components, structures and signaling molecules. Additionally, plasma membrane proteins comprise more than two-thirds of the known protein targets for existing drugs. Consequently, defining membrane proteomes is crucial to understanding the role of plasma membranes in fundamental biological processes and for finding new targets for action in drug development. MS-based identification methods combined with chromatographic and traditional cell-biology techniques are powerful tools for proteomic mapping of proteins from organelles. However, the separation and identification of plasma membrane proteins remains a challenge for proteomic technology because of their hydrophobicity and microheterogeneity Creative approaches to solve these problems and potential pitfalls will be discussed. Finally, a representative overview of the impressive achievements in this field will also be given.
引用
收藏
页码:3010 / 3029
页数:20
相关论文
共 283 条
[1]   Vectorial proteomics reveal targeting, phosphorylation and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes [J].
Aboulaich, N ;
Vainonen, JP ;
Strålfors, P ;
Vener, AV .
BIOCHEMICAL JOURNAL, 2004, 383 :237-248
[2]  
Albanese J, 1998, BLOOD, V91, P3862
[3]  
Alberts B., 2002, Molecular Biology of The Cell, V4th
[4]  
Albertson P. A., 1986, PARTITION CELL PARTI
[5]   Cell biology - A role for lipid shells in targeting proteins to caveolae, rafts, and other lipid domains [J].
Anderson, RGW ;
Jacobson, K .
SCIENCE, 2002, 296 (5574) :1821-1825
[6]   Proteomic analysis of the tetraspanin web using LC-ESI-MS/MS and MALDI-FTICR-MS [J].
André, M ;
Le Caer, JP ;
Greco, C ;
Planchon, S ;
El Nemer, W ;
Boucheix, C ;
Rubinstein, E ;
Chamot-Rooke, J ;
Le Naour, F .
PROTEOMICS, 2006, 6 (05) :1437-1449
[7]   Induction of lymphocyte apoptosis by tumor cell secretion of FasL-bearing microvesicles [J].
Andreola, G ;
Rivoltini, L ;
Castelli, C ;
Huber, V ;
Perego, P ;
Deho, P ;
Squarcina, P ;
Accornero, P ;
Lozupone, F ;
Lugini, L ;
Stringaro, A ;
Molinari, A ;
Arancia, G ;
Gentile, M ;
Parmiani, G ;
Fais, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (10) :1303-1316
[8]   Affinity chromatography: A useful tool in proteomics studies [J].
Azarkan, Mohamed ;
Huet, Joelle ;
Baeyens-Volant, Danielle ;
Looze, Yvan ;
Vandenbussche, Guy .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 849 (1-2) :81-90
[9]   Native proteomic analysis of protein complexes in murine intestinal brush border membranes [J].
Babusiak, Marek ;
Man, Petr ;
Petrak, Jiri ;
Vyoral, Daniel .
PROTEOMICS, 2007, 7 (01) :121-129
[10]   Lipid raft proteome reveals ATP synthase complex in the cell surface [J].
Bae, TJ ;
Kim, MS ;
Kim, JW ;
Kim, BW ;
Choo, HJ ;
Lee, JW ;
Kim, KB ;
Lee, CS ;
Kim, JH ;
Chang, SY ;
Kang, CY ;
Lee, SW ;
Ko, YG .
PROTEOMICS, 2004, 4 (11) :3536-3548