MAPPING OF RAS-RELATED GTP-BINDING PROTEINS BY GTP OVERLAY FOLLOWING 2-DIMENSIONAL GEL-ELECTROPHORESIS

被引:54
作者
HUBER, LA
ULLRICH, O
TAKAI, Y
LUTCKE, A
DUPREE, P
OLKKONEN, V
VIRTA, H
DEHOOP, MJ
ALEXANDROV, K
PETER, M
ZERIAL, M
SIMONS, K
机构
[1] EUROPEAN MOLEC BIOL LAB,CELL BIOL PROGRAMME,D-69117 HEIDELBERG,GERMANY
[2] KOBE UNIV,SCH MED,DEPT BIOCHEM,KOBE 650,JAPAN
[3] UNIV CAMBRIDGE,DEPT PLANT SCI,CAMBRIDGE CB2 3EA,ENGLAND
[4] GERMAN CANC RES CTR,TUMOR IMMUNOL PROGRAM,W-6900 HEIDELBERG,GERMANY
关键词
SYNAPTIC VESICLES; VESICULAR TRANSPORT; RAB; RHO; GDP DISSOCIATION INHIBITOR;
D O I
10.1073/pnas.91.17.7874
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
For identification of Rab, Rac, Rho, Ral, Rap, and Arf proteins on two-dimensional polyacrylamide gels, we have expressed full-length cDNAs of members of these protein families with the T7 RNA polymerase-recombinant vaccinia virus expression system. Membrane preparations from felts expressing the cDNAs were subjected to high-resolution two-dimensional polyacrylamide gel electrophoresis followed by [alpha-P-32]GTP ligand blotting. We have mapped 28 small GTP-binding proteins relative to their isoelectric points and according to their molecular weights and by immunoblot ting with specific antibodies. Rab and Rho proteins could be specifically identified by extraction of streptolysin O-permeabilized Madin-Darby canine kidney (MDCK) cells with Rab- and Rho-GDP dissociation inhibitor. We applied the reference mapping to analyze the GTP-binding patterns of synaptosome fractions from rat brain. The purified synaptosomes exhibited specific enrichment of Rab3a, Rab5a, Ral, and several other GTPases. This approach and the map we have produced should provide a useful aid for the analysis of the expression and localization of members of all families of small GTP-binding proteins in various cell types and subcellular fractions.
引用
收藏
页码:7874 / 7878
页数:5
相关论文
共 46 条
  • [1] EMERGING CONCEPTS IN THE RAS SUPERFAMILY OF GTP-BINDING PROTEINS
    BOKOCH, GM
    DER, CJ
    [J]. FASEB JOURNAL, 1993, 7 (09) : 750 - 759
  • [2] DO GTPASES DIRECT MEMBRANE TRAFFIC IN SECRETION
    BOURNE, HR
    [J]. CELL, 1988, 53 (05) : 669 - 671
  • [3] CELIS JE, 1993, ELECTROPHORESIS, V14, pU1091, DOI 10.1002/elps.11501401178
  • [4] LOCALIZATION OF LOW-MOLECULAR-WEIGHT GTP BINDING-PROTEINS TO EXOCYTIC AND ENDOCYTIC COMPARTMENTS
    CHAVRIER, P
    PARTON, RG
    HAURI, HP
    SIMONS, K
    ZERIAL, M
    [J]. CELL, 1990, 62 (02) : 317 - 329
  • [5] MOLECULAR-CLONING OF YPT1/SEC4-RELATED CDNAS FROM AN EPITHELIAL-CELL LINE
    CHAVRIER, P
    VINGRON, M
    SANDER, C
    SIMONS, K
    ZERIAL, M
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (12) : 6578 - 6585
  • [6] THE COMPLEXITY OF THE RAB AND RHO GTP-BINDING PROTEIN SUBFAMILIES REVEALED BY A PCR CLONING APPROACH
    CHAVRIER, P
    SIMONS, K
    ZERIAL, M
    [J]. GENE, 1992, 112 (02) : 261 - 264
  • [7] EXPRESSION AND LOCALIZATION OF 2 LOW-MOLECULAR-WEIGHT GTP-BINDING PROTEINS, RAB8 AND RAB10, BY EPITOPE TAG
    CHEN, YT
    HOLCOMB, C
    MOORE, HPH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) : 6508 - 6512
  • [8] A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX
    DEVEREUX, J
    HAEBERLI, P
    SMITHIES, O
    [J]. NUCLEIC ACIDS RESEARCH, 1984, 12 (01) : 387 - 395
  • [9] DOTTI CG, 1988, J NEUROSCI, V8, P1454
  • [10] ELFERINK LA, 1992, J BIOL CHEM, V267, P5768