Generation of branched actin networks: assembly and regulation of the N-WASP and WAVE molecular machines

被引:107
作者
Derivery, Emmanuel [1 ]
Gautreau, Alexis [1 ]
机构
[1] CNRS, UPR3082, Lab Enzymol & Biochim Struct, F-91198 Gif Sur Yvette, France
关键词
actin polymerization; Arp2/3; complex; nucleation promoting factors; molecular machines; ALDRICH-SYNDROME PROTEIN; ARP2/3; COMPLEX; MEMBRANE INVAGINATION; STRUCTURAL BASIS; CELL-MIGRATION; WIP COMPLEX; POLYMERIZATION; ACTIVATION; PHOSPHORYLATION; DOMAIN;
D O I
10.1002/bies.200900123
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 Arp2/3 complex is a molecular machine that generates branched actin networks responsible for membrane remodeling during cell migration, endocytosis, and other morphogenetic events. This machine requires activators, which themselves are multiprotein complexes. This review focuses on recent advances concerning the assembly of stable complexes containing the most-studied activators, N-WASP and WAVE proteins, and the level of regulation that is provided by these complexes. N-WASP is the paradigmatic auto-inhibited protein, which is activated by a conformational opening. Even though this regulation has been successfully reconstituted in vitro with isolated N-WASP, the native dimeric complex with a WIP family protein has unique additional properties. WAVE proteins are part of a pentameric complex, whose basal state and activated state when bound to the Rac GTPase were recently clarified. Moreover, this review attempts to put together diverse observations concerning the WAVE complex in the conceptual frame of an in vivo assembly pathway that has gained support from the recent identification of a precursor.
引用
收藏
页码:119 / 131
页数:13
相关论文
共 100 条
[1]   Membrane targeting of WAVE2 is not sufficient for WAVE2-dependent actin polymerization: a role for IRSp53 in mediating the interaction between Rac and WAVE2 [J].
Abou-Kheir, Wassim ;
Isaac, Beth ;
Yamaguchi, Hideki ;
Cox, Dianne .
JOURNAL OF CELL SCIENCE, 2008, 121 (03) :379-390
[2]   The cell as a collection of protein machines: Preparing the next generation of molecular biologists [J].
Alberts, B .
CELL, 1998, 92 (03) :291-294
[3]   Impairment of the ubiquitin-proteasome system by protein aggregation [J].
Bence, NF ;
Sampat, RM ;
Kopito, RR .
SCIENCE, 2001, 292 (5521) :1552-1555
[4]   PIR121 regulates pseudopod dynamics and SCAR activity in Dictyostelium [J].
Blagg, SL ;
Stewart, M ;
Sambles, C ;
Insall, RH .
CURRENT BIOLOGY, 2003, 13 (17) :1480-1487
[5]   Global disruption of the WASP autoinhibited structure on Cdc42 binding. Ligand displacement as a novel method for monitoring amide hydrogen exchange [J].
Buck, M ;
Xu, W ;
Rosen, MK .
BIOCHEMISTRY, 2001, 40 (47) :14115-14122
[6]   WHAMM is an Arp2/3 complex activator that binds microtubules and functions in ER to Golgi transport [J].
Campellone, Kenneth G. ;
Webb, Neil J. ;
Znameroski, Elizabeth A. ;
Welch, Matthew D. .
CELL, 2008, 134 (01) :148-161
[7]   Repetitive N-WASP-Binding Elements of the Enterohemorrhagic Escherichia coli Effector EspFU Synergistically Activate Actin Assembly [J].
Campellone, Kenneth G. ;
Cheng, Hui-Chun ;
Robbins, Douglas ;
Siripala, Anosha D. ;
McGhie, Emma J. ;
Hayward, Richard D. ;
Welch, Matthew D. ;
Rosen, Michael K. ;
Koronakis, Vassilis ;
Leong, John M. .
PLOS PATHOGENS, 2008, 4 (10)
[8]   GRB2 links signaling to actin assembly by enhancing interaction of neural Wiskott-Aldrich syndrome protein (N-WASp) with actin-related protein (ARP2/3) complex [J].
Carlier, MF ;
Nioche, P ;
Broutin-L'Hermite, I ;
Boujemaa, R ;
Le Clainche, C ;
Egile, C ;
Garbay, C ;
Ducruix, A ;
Sansonetti, P ;
Pantaloni, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (29) :21946-21952
[9]  
CHENG HC, 2008, NATURE
[10]   WIP regulates the stability and localization of WASP to podosomes in migrating dendritic cells [J].
Chou, Hsiu-Chuan ;
Anton, Ines M. ;
Holt, Mark R. ;
Curcio, Claudia ;
Lanzardo, Stefania ;
Worth, Austen ;
Burns, Siobhan ;
Thrasher, Adrian J. ;
Jones, Gareth E. ;
Calle, Yolanda .
CURRENT BIOLOGY, 2006, 16 (23) :2337-2344