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. 2005 Feb;17(2):486–501. doi: 10.1105/tpc.104.028555

Figure 7.

Figure 7.

VLN1 Stabilizes Actin Filaments against ADF.

Conditions: 10 mM Tris-HCl, pH 8, 50 mM KCl, 2 mM MgCl2, 1 mM EGTA, 0.2 mM ATP; 0.2 mM CaCl2, 0.5 mM DTT, and 3 mM NaN3 at 20°C.

(A) Time course of actin filament depolymerization monitored by pyrene fluorescence. Open squares, 1 μM actin filaments alone; open diamonds, 1 μM F-actin with 8 μM latrunculin B (LatB); open circles, 1 μM F-actin with 8 μM LatB and 1 μM VLN1; crosses, 1 μM F-actin with 0.6 μM ADF1, 8 μM LatB and 1 μM VLN1; and open triangles, 1 μM F-actin with 0.6 μM ADF1 and 8 μM LatB.

(B) Time course of actin polymerization (4 μM) monitored by pyrene fluorescence. Dashed line with no symbols, no additions to actin; open circles, actin with 1 μM VLN1; closed squares, actin with 1 μM ADF1; and open squares, actin with 1 μM VLN1 and 1 μM ADF1.