Dresden 2011 – scientific programme
Parts | Days | Selection | Search | Updates | Downloads | Help
BP: Fachverband Biologische Physik
BP 31: Posters: Biological Machines \& Motor Proteins
BP 31.1: Poster
Thursday, March 17, 2011, 17:15–20:00, P3
Neck-linker-length dependence of processive Kinesin-5 motility — •André Düselder, Christina Thiede, Stefanie Kramer, Christoph F. Schmidt, and Stefan Lakämper — Drittes Physikalisches Institut, Georg-August-Universität Göttingen, Germany
To explore the basic motor activity of the mitotic Kinesin-5, we previously constructed a stable dimeric Kinesin-5 head/Kinesin-1 stalk chimera (Eg5Kin), which contains the motor domain and 14 amino acids of the neck linker of Xenopus leavis Eg5 fused to the neck coiled coil of Drosophila melanogaster Kinesin-1. We have here investigated the effect of varying neck-linker length on the motile properties of Eg5Kin. We generated six Eg5Kin constructs comprising of 13 to up to the 18 amino acids of the native Eg5 neck linker, possibly providing a physiological context.
Using single-molecule fluorescence, we found that all six constructs are active motor molecules capable of processive motility. In a first set of experiments, we found that the neck-linker length influences the run length, but not the velocity of the motor. We thus confirm the findings of Shastry and Hancock (2010, Curr. Biol. 20:939) with a different motor. In addition we used optical-trap assays to investigate the change in the average force the motor constructs generated and found only a small variation. Our data thus suggest that the neck-linker length of Eg5 is at least not the sole determinant for speed and force generation.