22 research outputs found
Biological measurement beyond the quantum limit
Quantum noise places a fundamental limit on the per photon sensitivity
attainable in optical measurements. This limit is of particular importance in
biological measurements, where the optical power must be constrained to avoid
damage to the specimen. By using non-classically correlated light, we
demonstrated that the quantum limit can be surpassed in biological
measurements. Quantum enhanced microrheology was performed within yeast cells
by tracking naturally occurring lipid granules with sensitivity 2.4 dB beyond
the quantum noise limit. The viscoelastic properties of the cytoplasm could
thereby be determined with a 64% improved measurement rate. This demonstration
paves the way to apply quantum resources broadly in a biological context
Finding the Cell Center by a Balance of Dynein and Myosin Pulling and Microtubule Pushing: A Computational Study
By comparing computer modeling predictions with observations, we conclude that strong dynein and weaker myosin-generated forces pull the microtubules inward competing with microtubule plus-ends pushing the microtubule aster outward and that the balance of these forces positions the centrosome at the cell center
The Localization Transition of the Two-Dimensional Lorentz Model
We investigate the dynamics of a single tracer particle performing Brownian
motion in a two-dimensional course of randomly distributed hard obstacles. At a
certain critical obstacle density, the motion of the tracer becomes anomalous
over many decades in time, which is rationalized in terms of an underlying
percolation transition of the void space. In the vicinity of this critical
density the dynamics follows the anomalous one up to a crossover time scale
where the motion becomes either diffusive or localized. We analyze the scaling
behavior of the time-dependent diffusion coefficient D(t) including corrections
to scaling. Away from the critical density, D(t) exhibits universal
hydrodynamic long-time tails both in the diffusive as well as in the localized
phase.Comment: 13 pages, 7 figures
Mitotic redistribution of the mitochondrial network by Miro and Cenp-F
Although chromosome partitioning during mitosis is well studied, the molecular mechanisms that allow proper segregation of cytoplasmic organelles in human cells are poorly understood. Here we show that mitochondria interact with growing microtubule tips and are transported towards the daughter cell periphery at the end of mitosis. This phenomenon is promoted by the direct and cell cycle-dependent interaction of the mitochondrial protein Miro and the cytoskeletal-associated protein Cenp-F. Cenp-F is recruited to mitochondria by Miro at the time of cytokinesis and associates with microtubule growing tips. Cells devoid of Cenp-F or Miro show decreased spreading of the mitochondrial network as well as cytokinesis-specific defects in mitochondrial transport towards the cell periphery. Thus, Miro and Cenp-F promote anterograde mitochondrial movement and proper mitochondrial distribution in daughter cells