Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10870343 | FEBS Letters | 2014 | 6 Pages |
Abstract
The kinesin-13 family of microtubule depolymerases is a major regulator of microtubule dynamics. RNA interference-induced knockdown studies have highlighted their importance in many cell division processes including spindle assembly and chromosome segregation. Since microtubule turnovers and most mitotic events are relatively rapid (in minutes or seconds), developing tools that offer faster control over protein functions is therefore essential to more effectively interrogate kinesin-13 activities in living cells. Here, we report the identification and characterization of a selective allosteric kinesin-13 inhibitor, DHTP. Using high resolution microscopy, we show that DHTP is cell permeable and can modulate microtubule dynamics in cells.
Related Topics
Life Sciences
Agricultural and Biological Sciences
Plant Science
Authors
Lama Talje, Khaled Ben El Kadhi, Kaleem Atchia, Thierry Tremblay-Boudreault, Sébastien Carreno, Benjamin H. Kwok,