Intracellular transport of large cargoes, such as organelles, vesicles or large proteins, is a complex dynamical process that involves the interplay of ATP-consuming molecular motors, cytoskeleton filaments and the viscoelastic cytoplasm. The displacements of particles or probes in the cell cytoplasm as a function of time are characterized by different (anomalous) diffusion regimes. We investigate here the motion of pigment organelles (melanosomes) driven by myosin-V motors in \emph{Xenopus laevis} melanocytes using a high spatio-temporal resolution tracking technique. By analyzing the mean square displacement (MSD) of the obtained trajectories as a function of the time lag, we show that the melanosomes display a transition between subdiffusive to superdiffusive behavior. A stochastic theoretical model is introduced to generalize the interpretation of our data. Starting from a generalized Langevin equation that explicitly considers the collective action of the molecular motors we derive an analytical expression for the MSD as a function of the time lag, which also takes into account the experimental noise. By fitting our model to the experimental data we were able to discriminate the exponents that characterize the passive and active contributions to melanosome dynamics. The model also estimates the "global" motor forces correctly. In this sense, our model gives a quantitative description of active transport in living cells with a reduced number of parameters.
The efficiency of intracellular cargo transport from specific source to target locations is strongly dependent upon molecular motor-assisted motion along the cytoskeleton. Radial transport along microtubules and lateral transport along the filaments of the actin cortex underneath the cell membrane are characteristic for cells with a centrosome. The interplay between the specific cytoskeleton organization and the motor performance realizes a spatially inhomogeneous intermittent search strategy. In order to analyze the efficiency of such intracellular search strategies we formulate a random velo…
An accurate and efficient characterization of the polyelectrolyte properties for cytoskeleton filaments are key to the molecular understanding of electrical signal propagation, bundle and network formation, as well as other relevant physicochemical processes associated with biological functions in eukaryotic cells and their potential nanotechnological applications. In this article, we introduce an innovative multi-scale approach able to account for the atomistic details of a proteins molecular structure, its biological environment, and their impact on electrical impulses propagating along wild…
Intracellular transport is vital for the proper functioning and survival of a cell. Cargo (proteins, vesicles, organelles, etc.) is transferred from its place of creation to its target locations via molecular motor assisted transport along cytoskeletal filaments. The transport efficiency is strongly affected by the spatial organization of the cytoskeleton, which constitutes an inhomogeneous, complex network. In cells with a centrosome microtubules grow radially from the central microtubule organizing center towards the cell periphery whereas actin filaments form a dense meshwork, the actin cor…
The motility of adherent eukaryotic cells is driven by the dynamics of the actin cytoskeleton. Despite the common force-generating actin machinery, different cell types often show diverse modes of locomotion that differ in their shape dynamics, speed, and persistence of motion. Recently, experiments in Dictyostelium discoideum have revealed that different motility modes can be induced in this model organism, depending on genetic modifications, developmental conditions, and synthetic changes of intracellular signaling. Here, we report experimental evidence that in a mutated D. discoideum cell l…
Living cells dynamically modulate the local morphologies of their actin cytoskeletons to perform biological functions, including force transduction, intracellular transport, and cell division. A major challenge is to understand how diverse structures of the actin cytoskeleton are assembled from a limited set of molecular building blocks. Here we study the spontaneous self-assembly of a minimal model of cytoskeletal materials, consisting of semiflexible actin filaments, crosslinkers, and molecular motors. Using coarse-grained simulations, we demonstrate that by changing concentrations and kinet…
Actin cross-linking organizes basal body patterning through anomalous diffusion transitions
Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), Department of Biomedical Sciences, University of Copenhagen（哥本哈根大学生物医学科学系，诺和诺德基金会干细胞医学中心(reNEW)）；Biocomplexity, Niels Bohr Institute, Faculty of Science, University of Copenhagen（哥本哈根大学理学院尼尔斯·玻尔研究所生物复杂性研究中心）；Department of Civil Engineering, Indian Institute of Technology Bombay（印度孟买理工学院土木工程系）
The intracellular environment is a dynamic space filled with various organelles moving in all directions. Included in this diverse group of organelles are vesicles, which are involved in transport of molecular cargo throughout the cell. Vesicles move in either a directed or non-directed fashion, often depending on interactions with cytoskeletal proteins such as microtubules, actin filaments, and molecular motors. How these proteins affect the local fluctuations of vesicles in the cytoplasm is not clear since they have the potential to both facilitate and impede movement. Here we show that vesi…
