Vps9, Rabex-5 and DSS4:: Proteins with weak but distinct nucleotide-exchange activities for Rab proteins

被引:57
作者
Esters, H
Alexandrov, K
Iakovenko, A
Ivanova, T
Thomä, N
Rybin, V
Zerial, M
Scheidig, AJ
Goody, RS
机构
[1] Max Planck Inst Mol Physiol, Dept Phys Biochem, D-44227 Dortmund, Germany
[2] European Mol Biol Lab, D-69012 Heidelberg, Germany
关键词
Rab proteins; exchange factors; Vps9; Rabex-5; DSS4;
D O I
10.1006/jmbi.2001.4735
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
The activities of three Rab-specific factors with GDP/GTP exchange activity, Vps9p, Rabex-5 and DSS4, with their cognate GTPases, Ypt5lp, Rab5 and Ypt1p, have been analysed quantitatively. In contrast to other exchange factors examined and to DSS4, Vps9p, and by analogy probably Rabex-5, have considerably lower affinity than GDP to the respective GTPases. In keeping with this, they are relatively weak exchangers, with a maximal rate constant for GDP release from the ternary complex between exchange factor, GTPase and GDP of ca 0.01 s(-1), which is several orders of magnitude lower than for other exchange factors examined. If interaction with these proteins is a mandatory aspect of the Rab cycle, this suggests that the overall rate of cycling might be controlled at this point of the cycle. Surprisingly, DSS$, which has the thermodynamic potential to displace GDP effectively from Ypt1p, also does this very slowly, again with a maximal rate constant of ca 0.01 s(-1). An additional, and based on present knowledge, unique, feature of the Ypt1p.DSS4 complex, is that the association of GTP (or GDP) is more than 10(3)-fold slower than to Ypt1p, thus leading to a long life-time of the binary complex between the two proteins, even at the high nucleotide concentrations that prevail in the cell. This leads to the conclusion that the protein-protein complex is likely to have an important biological significance in addition to its probable role in GTP/GDP exchange. (C) 2001 Academic Press.
引用
收藏
页码:141 / 156
页数:16
相关论文
共 37 条
[1]   Identification of the catalytic domains and their functionally critical arginine residues of two yeast GTPase-activating proteins specific for Ypt/Rab transport GTPases [J].
Albert, S ;
Will, E ;
Gallwitz, D .
EMBO JOURNAL, 1999, 18 (19) :5216-5225
[2]   Two new members of a family of Ypt/Rab GTPase activating proteins - Promiscuity of substrate recognition [J].
Albert, S ;
Gallwitz, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (47) :33186-33189
[3]   Characterization of the ternary complex between Rab7, REP-1 and Rab geranylgeranyl transferase [J].
Alexandrov, K ;
Simon, I ;
Yurchenko, V ;
Iakovenko, A ;
Rostkova, E ;
Scheidig, AJ ;
Goody, RS .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 265 (01) :160-170
[4]   The retina [J].
Burdon, MA ;
Sanders, MD .
CURRENT OPINION IN NEUROLOGY, 1996, 9 (01) :16-20
[5]   CHARACTERIZATION OF A GUANINE NUCLEOTIDE-RELEASING FACTOR AND A GTPASE-ACTIVATING PROTEIN THAT ARE SPECIFIC FOR THE RAS-RELATED PROTEIN P25RAB3A [J].
BURSTEIN, ES ;
MACARA, IG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (04) :1154-1158
[6]   A MAMMALIAN GUANINE-NUCLEOTIDE-RELEASING PROTEIN ENHANCES FUNCTION OF YEAST SECRETORY PROTEIN SEC4 [J].
BURTON, J ;
ROBERTS, D ;
MONTALDI, M ;
NOVICK, P ;
DECAMILLI, P .
NATURE, 1993, 361 (6411) :464-467
[7]   SPECIFIC INTERACTIONS OF MSS4 WITH MEMBERS OF THE RAB GTPASE SUBFAMILY [J].
BURTON, JL ;
BURNS, ME ;
GATTI, E ;
AUGUSTINE, GJ ;
DECAMILLI, P .
EMBO JOURNAL, 1994, 13 (23) :5547-5558
[8]   An evolutionarily conserved domain in a subfamily of Rabs is crucial for the interaction with the guanyl nucleotide exchange factor Mss4 [J].
Burton, JL ;
Slepnev, V ;
DeCamilli, PV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (06) :3663-3668
[9]   The role of ARF and Rab GTPases in membrane transport [J].
Chavrier, P ;
Goud, B .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (04) :466-475
[10]   Interactions of nucleotide release factor Dss4p with Sec4p in the post-Golgi secretory pathway of yeast [J].
Collins, RN ;
Brennwald, P ;
Garrett, M ;
Lauring, A ;
Novick, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (29) :18281-18289