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. Author manuscript; available in PMC: 2008 Mar 3.
Published in final edited form as: Eur J Neurosci. 2007 Dec 4;26(12):3429–3436. doi: 10.1111/j.1460-9568.2007.05955.x

Fig. 2.

Fig. 2

Differential effects of tau phosphorylation by different protein kinases on its ability to stimulate microtubule (MT) assembly. Real-time MT assembly was monitored by measuring the turbidity (O.D.350 nm) of tubulin (2.0 mg/mL) at 35 °C in the presence of 0.07 mg/mL control-treated tau441 (Con-tau) or tau441 phosphorylated by dual-specificity tyrosine-phosphorylated and -regulated kinase 1A (Dyrk1A) (A), glycogen synthase kinase-3β (GSK-3β) (B) or cAMP-dependent protein kinase (PKA) (C). Representative real-time turbidimetric changes of MT assembly of three independent experiments with the same results are shown.