Details

Autor(en) / Beteiligte

• Komarova, Yulia
• De Groot, Christian O.
• Grigoriev, Ilya
• Gouveia, Susana Montenegro
• Munteanu, E. Laura
• Schober, Joseph M.
• Honnappa, Srinivas
• Buey, Rubén M.
• Hoogenraad, Casper C.
• Dogterom, Marileen
• Borisy, Gary G.
• Steinmetz, Michel O.
• Akhmanova, Anna

Titel

Mammalian End Binding Proteins Control Persistent Microtubule Growth

Ist Teil von

• The Journal of cell biology, 2009-03, Vol.184 (5), p.691-706

Ort / Verlag

United States: Rockefeller University Press

Erscheinungsjahr

2009

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• End binding proteins (EBs) are highly conserved core components of microtubule plus-end tracking protein networks. Here we investigated the roles of the three mammalian EBs in controlling microtubule dynamics and analyzed the domains involved. Protein depletion and rescue experiments showed that EB1 and EB3, but not EB2, promote persistent microtubule growth by suppressing catastrophes. Furthermore, we demonstrated in vitro and in cells that the EB plus-end tracking behavior depends on the calponin homology domain but does not require dimer formation. In contrast, dimerization is necessary for the EB anti-catastrophe activity in cells; this explains why the EB1 dimerization domain, which disrupts native EB dimers, exhibits a dominant-negative effect. When microtubule dynamics is reconstituted with purified tubulin, EBs promote rather than inhibit catastrophes, suggesting that in cells EBs prevent catastrophes by counteracting other microtubule regulators. This probably occurs through their action on microtubule ends, because catastrophe suppression does not require the EB domains needed for binding to known EB partners.