ATP-dependent membrane assembly of F-actin facilitates membrane fusion.

We recently established an in vitro assay that monitors the fusion between latex-bead phagosomes and endocytic organelles in the presence of J774 macrophage cytosol (). Here, we show that different reagents affecting the actin cytoskeleton can either inhibit or stimulate this fusion process. Because the membranes of purified phagosomes can assemble F-actin de novo from pure actin with ATP (), we focused here on the ability of membranes to nucleate actin in the presence of J774 cytosolic extracts. For this, we used F-actin sedimentation, pyrene actin assays, and torsional rheometry, a biophysical approach that could provide kinetic information on actin polymerization and gel formation. We make two major conclusions. First, under our standard in vitro conditions (4 mg/ml cytosol and 1 mM ATP), the presence of membranes actively catalyzed the assembly of cytosolic F-actin, which assembled into highly viscoelastic gels. A model is discussed that links these results to how the actin may facilitate fusion. Second, cytosolic actin paradoxically polymerized more under ATP depletion than under high-ATP conditions, even in the absence of membranes; we discuss these data in the context of the well described, large increases in F-actin seen in many cells during ischemia.

Viscoelastic properties of semiflexible filamentous bacteriophage fd.

The cytoskeletal protein filament F-actin has been treated in a number of recent studies as a model physical system for semiflexible filaments. In this work, we studied the viscoelastic properties of entangled solutions of the filamentous bacteriophage fd as an alternative to F-actin with similar physical parameters. We present both microrheometric and macrorheometric measurements of the viscoelastic storage and loss moduli, G'(f ) and G"(f ), respectively, in a frequency range 0.01

Microrheometry underestimates the values of the viscoelastic moduli in measurements on F-actin solutions compared to macrorheometry.

We present a systematic comparison of microrheological and macrorheological measurements of the viscoelastic storage and loss moduli, G'(f) and G"(f), respectively, of solutions of the semiflexible biopolymer F-actin. Using magnetic tweezers microrheometry and rotating disk macrorheometry, we show that microscopic values for G'(f) and G"(f) are significantly smaller than macroscopic results over the frequency range f = 0.004-4 Hz, whereas the qualitative shape of the spectra is similar. These findings confirm recent theoretical predictions [A. C. Maggs, Phys. Rev. E 57, 2091 (1998)]. The discrepancy affects not only absolute values of G'(f) and G"(f): although microscopic and macroscopic plateau regime are found in the same frequency range, the two methods yield different values for the entanglement time which determines the high-frequency end of the plateau. By investigating F-actin solutions of different mean filament lengths, we show that microscopic and macroscopic G'(f) and G"(f) converge, if the probe particle used in microrheometry becomes large compared to the length of actin filaments.