182 research outputs found
âEntropic Trapsâ in the Kinetics of Phase Separation in Multicomponent Membranes Stabilize Nanodomains
AbstractWe quantitatively describe the creation and evolution of phase-separated domains in a multicomponent lipid bilayer membrane. The early stages, termed the nucleation stage and the independent growth stage, are extremely rapid (characteristic times are submillisecond and millisecond, respectively) and the system consists of nanodomains of average radius âŒ5â50nm. Next, mobility of domains becomes consequential; domain merger and fission become the dominant mechanisms of matter exchange, and line tension Îł is the main determinant of the domain size distribution at any point in time. For sufficiently small Îł, the decrease in the entropy term that results from domain merger is larger than the decrease in boundary energy, and only nanodomains are present. For large Îł, the decrease in boundary energy dominates the unfavorable entropy of merger, and merger leads to rapid enlargement of nanodomains to radii of micrometer scale. At intermediate line tensions and within finite times, nanodomains can remain dispersed and coexist with a new global phase. The theoretical critical value of line tension needed to rapidly form large rafts is in accord with the experimental estimate from the curvatures of budding domains in giant unilamellar vesicles
Electrohydrodynamic model of vesicle deformation in alternating electric fields
We develop an analytical theory to explain the experimentally-observed
morphological transitions of giant vesicles induced by AC electric fields (1).
The model treats the inner and suspending media as lossy dielectrics, while the
membrane as an ion-impermeable flexible incompressible-fluid sheet. The vesicle
shape is obtained by balancing electric, hydrodynamic, and bending stresses
exerted on the membrane. Considering a nearly spherical vesicle, the solution
to the electrohydrodynamic problem is obtained as a regular perturbation
expansion in the excess area.
The theory predicts that stationary vesicle deformation depends on field
frequency and conductivity conditions. If the inner fluid is more conducting
than the suspending medium, the vesicle always adopts a prolate shape. In the
opposite case, the vesicle undergoes a transition from a prolate to oblate
ellipsoid at a critical frequency, which the theory identifies with the inverse
membrane charging time. At frequencies higher than the inverse Maxwell-Wagner
polarization time, the electrohydrodynamic stresses become too small to alter
the vesicle's quasi-spherical rest shape. The analysis shows that the evolution
towards the stationary vesicle deformation strongly depends on membrane
properties such as viscosity. The model can be applied to rationalize the
transient and steady deformation of biological cells in electric fields
Skin Impedance Measurements for Acupuncture Research: Development of a Continuous Recording System
Skin impedance at acupuncture points (APs) has been used as a diagnostic/therapeutic aid for more than 50 years. Currently, researchers are evaluating the electrophysiologic properties of APs as a possible means of understanding acupuncture's mechanism. To comprehensively assess the diagnostic, therapeutic and mechanistic implications of acupuncture point skin impedance, a device capable of reliably recording impedances from 100 kΩ to 50 MΩ at multiple APs over extended time periods is needed. This article describes design considerations, development and testing of a single channel skin impedance system (hardware, control software and customized electrodes). The system was tested for accuracy against known resistors and capacitors. Two electrodes (the AMI and the ORI) were compared for reliability of recording over 30 min. Two APs (LU 9 and PC 6) and a nearby non-AP site were measured simultaneously in four individuals for 60 min. Our measurement system performed accurately (within 5%) against known resistors (580 kΩâ10 MΩ) and capacitors (10 nFâ150 nF). Both the AMI electrode and the modified ORI electrode recorded skin impedance reliably on the volar surface of the forearm (r = 0.87 and r = 0.79, respectively). In four of four volunteers tested, skin impedance at LU 9 was less than at the nearby non-AP site. In three of four volunteers skin impedance was less at PC 6 than at the nearby non-AP site. We conclude that our system is a suitable device upon which we can develop a fully automated multi-channel device capable of recording skin impedance at multiple APs simultaneously over 24 h
The Salivary Secretome of the Tsetse Fly Glossina pallidipes (Diptera: Glossinidae) Infected by Salivary Gland Hypertrophy Virus
Tsetse fly (Diptera; Glossinidae) transmits two devastating diseases to farmers (human African Trypanosomiasis; HAT) and their livestock (Animal African Trypanosomiasis; AAT) in 37 sub-Saharan African countries. During the rainy seasons, vast areas of fertile, arable land remain uncultivated as farmers flee their homes due to the presence of tsetse. Available drugs against trypanosomiasis are ineffective and difficult to administer. Control of the tsetse vector by Sterile Insect Technique (SIT) has been effective. This method involves repeated release of sterilized males into wild tsetse populations, which compete with wild type males for females. Upon mating, there is no offspring, leading to reduction in tsetse populations and thus relief from trypanosomiasis. The SIT method requires large-scale tsetse rearing to produce sterile males. However, tsetse colony productivity is hampered by infections with the salivary gland hypertrophy virus, which is transmitted via saliva as flies take blood meals during membrane feeding and often leads to colony collapse. Here, we investigated the salivary gland secretome proteins of virus-infected tsetse to broaden our understanding of virus infection, transmission and pathology. By this approach, we obtain insight in tsetse-hytrosavirus interactions and identified potential candidate proteins as targets for developing biotechnological strategies to control viral infections in tsetse colonies
- âŠ