Phosphorylation of non-muscle myosin II regulatory light chain by p21-activated kinase (γ-PAK)

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作者：

TL Chew，RA Masaracchia，ZM Goeckeler，RB Wysolmerski

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摘要：

Myosin regulatory light chain (RLC) phosphorylation has been implicated in Rho-mediated stress fibre formation. The recent observation that Rho kinase phosphorylates RLC in vitro suggests that serine/threonine kinases other than those in the myosin light chain kinase (MLCK) family have the potential to activate myosin II. In this study we report that γ-PAK, which is activated by the GTP-binding proteins Cdc42 and Rac, catalyses phosphorylation of intact non-muscle myosin II and isolated recombinant RLC. γ- PAK phosphorylated endothelial cell myosin II to 0.85±0.02mol PO4 per mol RLC. Phosphorylation is Ca2+/calmodulin-independent and the enzyme has a Km and Vmax for myosin II regulatory light chain of 12μm and 180nmol/min/mg respectively. No myosin II heavy chain phosphorylation was detected. Phosphopeptide maps and phosphoamino acid analysis revealed that γ-PAK phosphorylates Ser-19 but does not phosphorylate Thr-18. A panel of recombinant RLC mutants was used to confirm that Ser-19 is the only phosphorylation site modified by γ-PAK. On substitution of both Ser-19 and Thr-18 with Ala or Glu, no phosphorylation of other Ser/Thr residues in the RLC was detected. Similar to MLCK, Arg-16 is required for interaction of γ-PAK with the substrate, since converting Arg-16 to Ala significantly reduced RLC phosphorylation. Endothelial cell monolayers permeabilized with saponin retract upon exposure to either Cdc42 or trypsin-activated γ-PAK and ATP. Activation of γ-PAK is required to initiate Ca2+/calmodulin-independent cell retraction and actin rearrangement. Taken together, these data suggest that myosin II activation by the p21-activated family of kinases may be physiologically important in regulating cytoskeletal organization.

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关键词：

Animals Cattle Pulmonary Artery Cells, Cultured Myosins Myosin Light Chains Recombinant Proteins Substrate Specificity Phosphorylation Gene Expression