114 research outputs found
Collisional Effects on Fast Electron Generation and Transport in Fast Ignition
As the binary collision process requires much more computation time, a statistical electron-electron collision model based on modified Langevin equation is developed to reduce it. This collision model and a simple electron-ion scattering model are installed into one-dimensional PIC code, and collisional effects on fast electron generation and transport in fast ignition are investigated. In the collisional case, initially thermal electrons are heated up to a few hundred keV due to direct energy transfer by electron-electron collision, and they are also heated up to MeV by Joule heating induced by electron-ion scattering. Thus the number of low energy component of fast electrons increase than that in the collisionless case
Prime movers : mechanochemistry of mitotic kinesins
Mitotic spindles are self-organizing protein machines that harness teams of multiple force generators to drive chromosome segregation. Kinesins are key members of these force-generating teams. Different kinesins walk directionally along dynamic microtubules, anchor, crosslink, align and sort microtubules into polarized bundles, and influence microtubule dynamics by interacting with microtubule tips. The mechanochemical mechanisms of these kinesins are specialized to enable each type to make a specific contribution to spindle self-organization and chromosome segregation
Processive Movement by a Kinesin Heterodimer with an Inactivating Mutation in One Head†
ABSTRACT: A single molecule of the motor enzyme kinesin-1 keeps a tight grip on its microtubule track, making tens or hundreds of discrete, unidirectional 8 nm steps before dissociating. This high duty ratio processive movement is thought to require a mechanism in which alternating stepping of the two head domains of the kinesin dimer is driven by alternating, overlapped cycles of ATP hydrolysis by the two heads. The R210K point mutation in Drosophila kinesin heavy chain was reported to disrupt the ability of the enzyme active site to catalyze ATP P-O bond cleavage. We expressed R210K homodimers as well as isolated R210K heads and confirmed that both are essentially inactive. We then coexpressed tagged R210K subunits with untagged wild-type subunits and affinity purified R210K/wild-type heterodimers together with the inactive R210K homodimers. In contrast to the R210K head or homodimer, the heterodimer was a highly active (>50 % of wild-type) microtubule-stimulated ATPase, and the heterodimer displayed high duty ratio processive movement in single-molecule motility experiments. Thus, dimerization of a subunit containing the inactivating mutation with a functional subunit can complement the mutation; this must occur either by lowering or by bypassing kinetic barriers in the ATPase or mechanical cycles of the mutant head. The observations provide support for kinesin-1 gating mechanisms in which one head stimulates the rate of essential processes in the other
Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer
Influência de fatores genéticos e ambientais sobre características reprodutivas do rebanho eqüino do Exército Brasileiro
Outcome of sleepiness and fatigue scores in obstructive sleep apnea syndrome patients with and without restless legs syndrome after nasal CPAP
- …