4,874 research outputs found

    Molecular Electroporation and the Transduction of Oligoarginines

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    Certain short polycations, such as TAT and polyarginine, rapidly pass through the plasma membranes of mammalian cells by an unknown mechanism called transduction as well as by endocytosis and macropinocytosis. These cell-penetrating peptides (CPPs) promise to be medically useful when fused to biologically active peptides. I offer a simple model in which one or more CPPs and the phosphatidylserines of the inner leaflet form a kind of capacitor with a voltage in excess of 180 mV, high enough to create a molecular electropore. The model is consistent with an empirical upper limit on the cargo peptide of 40--60 amino acids and with experimental data on how the transduction of a polyarginine-fluorophore into mouse C2C12 myoblasts depends on the number of arginines in the CPP and on the CPP concentration. The model makes three testable predictions.Comment: 15 pages, 5 figure

    Adhesion-induced lateral phase separation of multi-component membranes: the effect of repellers and confinement

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    We present a theoretical study for adhesion-induced lateral phase separation for a membrane with short stickers, long stickers and repellers confined between two hard walls. The effects of confinement and repellers on lateral phase separation are investigated. We find that the critical potential depth of the stickers for lateral phase separation increases as the distance between the hard walls decreases. This suggests confinement-induced or force-induced mixing of stickers. We also find that stiff repellers tend to enhance, while soft repellers tend to suppress adhesion-induced lateral phase separation

    Sequence Heterogeneity Accelerates Protein Search for Targets on DNA

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    The process of protein search for specific binding sites on DNA is fundamentally important since it marks the beginning of all major biological processes. We present a theoretical investigation that probes the role of DNA sequence symmetry, heterogeneity and chemical composition in the protein search dynamics. Using a discrete-state stochastic approach with a first-passage events analysis, which takes into account the most relevant physical-chemical processes, a full analytical description of the search dynamics is obtained. It is found that, contrary to existing views, the protein search is generally faster on DNA with more heterogeneous sequences. In addition, the search dynamics might be affected by the chemical composition near the target site. The physical origins of these phenomena are discussed. Our results suggest that biological processes might be effectively regulated by modifying chemical composition, symmetry and heterogeneity of a genome.Comment: 10 pages, 5 figure

    Nematic and Polar order in Active Filament Solutions

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    Using a microscopic model of interacting polar biofilaments and motor proteins, we characterize the phase diagram of both homogeneous and inhomogeneous states in terms of experimental parameters. The polarity of motor clusters is key in determining the organization of the filaments in homogeneous isotropic, polarized and nematic states, while motor-induced bundling yields spatially inhomogeneous structures.Comment: 4 pages. 3 figure

    Effective temperature of active matter

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    We follow the dynamics of an ensemble of interacting self-propelled motorized particles in contact with an equilibrated thermal bath. We find that the fluctuation-dissipation relation allows for the definition of an effective temperature that is compatible with the results obtained using a tracer particle as a thermometer. The effective temperature takes a value which is higher than the temperature of the bath and it is continuously controlled by the motor intensity

    Dry and wet interfaces: Influence of solvent particles on molecular recognition

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    We present a coarse-grained lattice model to study the influence of water on the recognition process of two rigid proteins. The basic model is formulated in terms of the hydrophobic effect. We then investigate several modifications of our basic model showing that the selectivity of the recognition process can be enhanced by considering the explicit influence of single solvent particles. When the number of cavities at the interface of a protein-protein complex is fixed as an intrinsic geometric constraint, there typically exists a characteristic fraction that should be filled with water molecules such that the selectivity exhibits a maximum. In addition the optimum fraction depends on the hydrophobicity of the interface so that one has to distinguish between dry and wet interfaces.Comment: 11 pages, 7 figure

    The Impact of an Enacted Social Support Training Intervention on Worklife Interaction and Stress in a Sample of Working Adults

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    The present investigation explores utilizes an enacted social support intervention among a group of working adults. Reductions in psychological and physiological stress were hypothesized to occur following the experimental intervention. Participants (N = 46) were all full time staff members at a large university and were randomly assigned to treatment or wait-list control groups. Treatment group members attended two 90 minute enacted social support meetings over the course of four weeks. Psychological (perceived stress and worklife conflict) and physiological (salivary cortisol) data were collected at both pretest and posttest periods. Results did not support the research hypotheses; however, a research question exploring the buffering effect of enacted support was answered in the affirmative. Enacted social support moderated the relationship between psychological and physiological stress at the pretest. The discussion presents a detailed assessment of theoretical and practical applications as well as suggestions for utilizing field social support interventions

    Polymer Release out of a Spherical Vesicle through a Pore

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    Translocation of a polymer out of curved surface or membrane is studied via mean first passage time approach. Membrane curvature gives rise to a constraint on polymer conformation, which effectively drives the polymer to the outside of membrane where the available volume of polymer conformational fluctuation is larger. Considering a polymer release out of spherical vesicle, polymer translocation time τ\tau is changed to the scaling behavior τL2\tau\sim L^2 for R<RGR<R_G, from τL3\tau\sim L^3 for RRGR\gg R_G, where LL is the polymer contour length and RR, RGR_G are vesicle radius and polymer radius of gyration respectively. Also the polymer capture into a spherical budd is studied and possible apparatus for easy capture is suggested.Comment: 14 pages RevTeX, 6 postscript figures, published in Phys. Rev. E 57, 730 (1998
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