FIGURE 5.

Contraction and LC₂₀ diphosphorylation in Triton-skinned rat caudal arterial smooth muscle in response to microcystin at pCa 4.5. A, Triton-skinned rat caudal arterial smooth muscle strips mounted on a force transducer in pCa 9 solution were treated with microcystin (1 μm) at pCa 4.5. Separate tissues were harvested at the indicated times during the contraction for analysis of LC₂₀ phosphorylation by Phos-tag SDS-PAGE and Western blotting (B) with antibodies to LC₂₀ (panel a), Ser(P)¹⁹-LC₂₀ (panel b), Thr(P)¹⁸-LC₂₀ (panel c), and Thr(P)¹⁸,Ser(P)¹⁹-LC₂₀ (panel d). Numbers below the gel lanes correspond to the time points in A. C, cumulative quantitative data showing the proportions of unphosphorylated (0P, closed circles), mono- (1P, open circles), and diphosphorylated LC₂₀ (2P, closed inverted triangles) as a function of time. Values represent the mean ± S.E. (n = 3).