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. Author manuscript; available in PMC: 2010 May 10.
Published in final edited form as: Trends Cell Biol. 2008 May 29;18(7):307–310. doi: 10.1016/j.tcb.2008.05.003

Table 1.

Effect of Kinesin-8 on microtubule-shortening rate and catastrophe frequency

Parameter Experiment type and organism With Kinesin-8a Without Kinesin-8b
Microtubule-shortening rate (μm/min) In vivo: budding yeast astral microtubules 1.91 ± 0.69 [16] 2.82 ± 0.95 [16]
In vivo, human (HeLa cells) 1.92 ± 0.06 [15] (metaphase) 2.80 ± 0.08 [15] (metaphase)
1.68 ± 0.08 [15] (anaphase) 2.12 ± 0.14 [15] (anaphase)
In vitro, GMPCPP microtubules ~0.10 [16] (50 nM Kip3p) ~0.00 [16]
~0.50 [8] (3.3 nM Kip3p) ~0.00 [8]
In vitro, GMPCPP microtubules ~1.25 [9] (100 nM Kif18A) ~0.00 [9]
Microtubule catastrophe frequency (min−1) In vivo, budding yeast astral microtubules 0.48 [16] 0.27 [16]
a

Kinesin-8 molecular motors are present in the assay, either endogenously as in the in vivo studies, or added to the assay in the noted concentrations as in the in vitro studies.

b

Kinesin-8 molecular motors are either deleted or knocked down as in the in vivo studies, or absent as in the in vitro studies.