A “molecular guillotine” reveals an interphase function of Kinesin-5

Author:

Lv Zhiyi1,Rosenbaum Jan2,Aspelmeier Timo2,Großhans Jörg1

Affiliation:

1. Institute for Developmental Biochemistry, Medical School, University of Göttingen, Justus-von-Liebig Weg 11, 37077 Göttingen, Germany

2. Institute for Mathematical Stochastics and Felix Bernstein Institute for Mathematical Statistics in the Biosciences, University of Göttingen, Goldschmidtstraße 7, 37077 Göttingen, Germany

Abstract

Motor proteins are important for transport and force generation in a variety of cellular processes and morphogenesis. Here we design a general strategy for conditional motor mutants by inserting a protease cleavage site into the “neck” between the head domain and the stalk of the motor protein, making the protein susceptible to proteolytic cleavage at the neck by the corresponding protease. To demonstrate the feasibility of this approach, we inserted the cleavage site of TEV protease into the neck of the tetrameric motor Kinesin-5. Application of TEV protease led to a specific depletion and functional loss of Kinesin-5 in Drosophila embryos. With our approach, we revealed that Kinesin-5 stabilized the microtubule network during interphase in syncytial embryos. The “molecular guillotine” can potentially be applied to many motor proteins due to the conserved structures of kinesins and myosins with accessible necks.

Funder

Deutsche Forschungsgemeinschaft

Publisher

The Company of Biologists

Subject

Cell Biology

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