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. 2010 Jun 16;30(24):8214–8220. doi: 10.1523/JNEUROSCI.1469-10.2010

Figure 3.

Figure 3.

tatCN21 inhibits stimulated and autonomous CaMKII activity with equally high potency and efficacy. A, tatCN21 potently inhibited Ca2+/CaM-stimulated CaMKII (2.5 nm) activity toward the peptide substrate syntide 2 (75 μm). The calculated IC50 was ∼40 nm. B, tatCN21 inhibited stimulated and autonomous CaMKII activity with equal potency (as indicated by identical inhibition at 40 nm, the IC50 calculated from A) and efficacy (as indicated by complete block of inhibition at 5 μm, 120-fold of IC50), while stimulated activity of the related CaMKIV was not affected at all. Error bars indicate SEM in all panels.