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Conformational changes in the Arp2/3 complex leading to actin nucleation
被引:0
|作者:
Avital A Rodal
Olga Sokolova
Deborah B Robins
Karen M Daugherty
Simon Hippenmeyer
Howard Riezman
Nikolaus Grigorieff
Bruce L Goode
机构:
[1] Rosenstiel Basic Medical Sciences Research Center,Department of Biology
[2] Brandeis University,Howard Hughes Medical Institute and Department of Biochemistry
[3] Rosenstiel Basic Medical Sciences Research Center,Department of Cell Biology
[4] Brandeis University,Department of Biochemistry
[5] Biozentrum,undefined
[6] University of Basel,undefined
[7] University of Geneva,undefined
[8] Sciences II,undefined
[9] 30 Quai E. Ansermet,undefined
来源:
Nature Structural & Molecular Biology
|
2005年
/
12卷
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摘要:
The two actin-related subunits of the Arp2/3 complex, Arp2 and Arp3, are proposed to form a pseudo actin dimer that nucleates actin polymerization. However, in the crystal structure of the inactive complex, they are too far apart to form such a nucleus. Here, we show using EM that yeast and bovine Arp2/3 complexes exist in a distribution among open, intermediate and closed conformations. The crystal structure docks well into the open conformation. The activator WASp binds at the cleft between Arp2 and Arp3, and all WASp-bound complexes are closed. The inhibitor coronin binds near the p35 subunit, and all coronin-bound complexes are open. Activating and loss-of-function mutations in the p35 subunit skew conformational distribution in opposite directions, closed and open, respectively. We conclude that WASp stabilizes p35-dependent closure of the complex, holding Arp2 and Arp3 closer together to nucleate an actin filament.
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页码:26 / 31
页数:5
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