Binding, activation and dissociation of the dimeric SecA ATPase at the dimeric SecYEG translocase

被引:109
作者
Duong, F [1 ]
机构
[1] Univ Paris 11, CNRS, Lab Transports & Signalisat Cellulaires, UMR 8619, F-91405 Orsay, France
关键词
ATPase; channel; oligomerization; preprotein translocation; SecA; SecYEG;
D O I
10.1093/emboj/cdg418
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 bacterial preprotein translocase is comprised of a membrane-embedded oligomeric SecYEG structure and a cytosolic dimeric SecA ATPase. The associations within SecYEG oligomers and SecA dimers, as well as between these two domains are dynamic and reversible. Here, it is shown that a covalently linked SecYEG dimer forms a functional translocase and a high affinity binding site for monomeric and dimeric SecA in solution. The interaction between these two domains stimulates the SecA ATPase, and nucleotides modulate the affinity and ratio of SecA monomers and dimers bound to the linked SecYEG complex. During the translocation reaction, the SecA monomer remains in stable association with a SecYEG protomer and the translocating preprotein. The nucleotides and translocation-dependent changes of SecA-SecYEG associations and the SecA dimeric state may reflect important facets of the preprotein translocation reaction.
引用
收藏
页码:4375 / 4384
页数:10
相关论文
共 43 条
[1]   Phospholipid-induced monomerization and signal-peptide-induced oligomerization of SecA [J].
Benach, J ;
Chou, YT ;
Fak, JJ ;
Itkin, A ;
Nicolae, DD ;
Smith, PC ;
Wittrock, G ;
Floyd, DL ;
Golsaz, CM ;
Gierasch, LM ;
Hunt, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :3628-3638
[2]   The SecYEG preprotein translocation channel is a conformationally dynamic and dimeric structure [J].
Bessonneau, P ;
Besson, V ;
Collinson, I ;
Duong, F .
EMBO JOURNAL, 2002, 21 (05) :995-1003
[3]   THE C-TERMINUS OF SECA IS INVOLVED IN BOTH LIPID-BINDING AND SECB BINDING [J].
BREUKINK, E ;
NOUWEN, N ;
VANRAALTE, A ;
MIZUSHIMA, S ;
TOMMASSEN, J ;
DEKRUIJFF, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (14) :7902-7907
[4]   Three-dimensional structure of the bacterial protein-translocation complex SecYEG [J].
Breyton, C ;
Haase, W ;
Rapoport, TA ;
Kühlbrandt, W ;
Collinson, I .
NATURE, 2002, 418 (6898) :662-665
[5]   The general protein secretory pathway: phylogenetic analyses leading to evolutionary conclusions [J].
Cao, TB ;
Saier, MH .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1609 (01) :115-125
[6]   Projection structure and oligomeric properties of a bacterial core protein translocase [J].
Collinson, I ;
Breyton, C ;
Duong, F ;
Tziatzios, C ;
Schubert, D ;
Or, E ;
Rapoport, T ;
Kühlbrandt, W .
EMBO JOURNAL, 2001, 20 (10) :2462-2471
[7]   The ATPase domain of SecA can form a tetramer in solution [J].
Dempsey, BR ;
Economou, A ;
Dunn, SD ;
Shilton, BH .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 315 (04) :831-843
[8]   SECA, THE PERIPHERAL SUBUNIT OF THE ESCHERICHIA-COLI PRECURSOR PROTEIN TRANSLOCASE, IS FUNCTIONAL AS A DIMER [J].
DRIESSEN, AJM .
BIOCHEMISTRY, 1993, 32 (48) :13190-13197
[9]   Distinct catalytic roles of the SecYE, SecG and SecDFyajC subunits of preprotein translocase holoenzyme [J].
Duong, F ;
Wickner, W .
EMBO JOURNAL, 1997, 16 (10) :2756-2768
[10]   The PrlA and PrlG phenotypes are caused by a loosened association among the translocase SecYEG subunits [J].
Duong, F ;
Wickner, W .
EMBO JOURNAL, 1999, 18 (12) :3263-3270