Addition of GTPγS and recombinant Cdc42 induced actin polymerization in a cell-free system, a process requiring GTPγS binding and limited by guanine nucleotide exchange.
Demonstrates that Cdc42 and GTPgammaS regulate actin polymerization in a cell-free system via mechanisms limited by guanine nucleotide exchange.
We have established a cell-free system to investigate pathways that regulate actin polymerization. Addition of GTPgammaS to lysates of polymorphonuclear leukocytes (PMNs) or Dictyostelium discoideum amoeba induced formation of filamentous actin. The GTPgammaS appeared to act via a small G-protein, since it was active in lysates ofD. discoideum mutants missing either the alpha2- or beta-subunit of the heterotrimeric G-protein required for chemoattractant-induced actin polymerization in living cells. Furthermore, recombinant Cdc42, but not Rho or Rac, induced polymerization in the cell-free system. The Cdc42-induced increase in filamentous actin required GTPgammaS binding and was inhibited by a fragment of the enzyme PAK1 that binds Cdc42. In a high speed supernatant, GTPgammaS alone was ineffective, but GTPgammaS-loaded Cdc42 induced actin polymerization, suggesting that the response was limited by guanine nucleotide exchange. Stimulating exchange by chelating magnesium, by adding acidic phospholipids, or by adding the exchange factors Cdc24 or Dbl restored the ability of GTPgammaS to induce polymerization. The stimulation of actin polymerization did not correlate with PIP2 synthesis.
Zigmond et al. (Mon,) reported a other. GTPγS and Cdc42 was evaluated on Actin polymerization. Addition of GTPγS and recombinant Cdc42 induced actin polymerization in a cell-free system, a process requiring GTPγS binding and limited by guanine nucleotide exchange.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: