Résumé
The Wave proteins are major activators of the Arp2/3 complex. The ubiquitous Wave-2 is required for actin polymerization at the leading edge of migrating cells. Here we purify Wave-2 from HeLa cells. Five proteins, Sra, Nap, Wave-2, Abi, and Hspc, are copurified, indicating that they form a tight complex. These proteins are only present in the complexed form, with the exception of Hspc, which displays a free pool. We reconstitute the Wave-2 complex by cotranslating in vitro the five subunits and use this system together with specific immunoprecipitations to study the molecular architecture of the complex. The complex is organized around a core of Nap and Abi. Sra is a peripheral subunit recruited on the Nap side, whereas the Wave and Hspc subunits are recruited on the Abi side of the core.
| langue originale | Anglais |
|---|---|
| Pages (de - à) | 4379-4383 |
| Nombre de pages | 5 |
| journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 101 |
| Numéro de publication | 13 |
| Les DOIs | |
| état | Publié - 30 mars 2004 |
| Modification externe | Oui |
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