Use of live cell imaging of vaccinia virus-infected cells with fluorescence bleaching shows that the turnover rate of N-WASP (an activator of the ARP2/3 complex) is inversely proportional to the rate of actin-based motility of the virus. Actin polymerization is also required to promote N-WASP turnover on the virus. These observations are consistent with a model in which the stability of N-WASP association beneath the virus controls the overall rate of Arp2/3 complex-dependent actin-based motility.
- Ina Weisswange
- Timothy P. Newsome
- Michael Way