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The Effect of Polysialic Acid Expression on Glioma Cell Nano-mechanicsGrant, Colin A., Twigg, Peter C., Saeed, Rida F., Lawson, G., Falconer, Robert A., Shnyder, Steven 03 January 2016 (has links)
Yes / Polysialic acid (PolySia) is an important carbohydrate bio-polymer that is commonly over-expressed on tumours of neuroendocrine origin and plays a key role in tumour progression. PolySia exclusively decorates the neural cell adhesion molecule (NCAM) on tumour cell membranes, modulating cell-cell interactions, motility and invasion. In this preliminary study, we examine the nano-mechanical properties of isogenic C6 rat glioma cells - transfected cells engineered to express the enzyme polysialyltransferase ST8SiaII, which synthesises polySia (C6-STX cells) and wild type cells (C6-WT). We demonstrate that polySia expression leads to reduced elastic and adhesive properties but also more visco-elastic compared to non-expressing wild type cells. Whilst differences in cell elasticity between healthy and cancer cells is regularly assigned to changes in the cytoskeleton, we show that in this model system the change in properties at the nano-level is due to the polySia on the transfected cell membrane surface.
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Temperature dependent stiffness and visco-elastic behaviour of lipid coated microbubbles using atomic force microscopy.Grant, Colin A., McKendry, J.E., Evans, S.D. 03 November 2011 (has links)
Yes / The compression stiffness of a phospholipid microbubble was determined using force-spectroscopy as a function of temperature. The stiffness was found to decrease by approximately a factor of three from 0.08 N m 1, at 10 C, down to 0.03 N m 1 at 37 C. This temperature dependence indicates that the surface tension of lipid coating is the dominant contribution to the microbubble stiffness. The timedependent material properties, e.g. creep, increased non-linearly with temperature, showing a factor of two increase in creep-displacement, from 24 nm, at 10 C, to 50 nm, at 37 C. The standard linear solid model was used to extract the visco-elastic parameters and their determination at different temperatures allowed the first determination of the activation energy for creep, for a microbubble, to be determined. / EPSRC
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Optomechanics and nonlinear mechanics of suspended photonic crystal membranesHui, Pui Chuen 01 January 2015 (has links)
The recent demonstration of strong interactions between optical force and mechanical motion of an optomechanical structure has led to the triumphant result of mechanical ground-state cooling, where the quantum nature of a macroscopic object is revealed. Another intriguing demonstration of quantum physics on a macroscopic level is the measurement of the Casimir force which is a manifestation of the zero- point energy. An interesting aspect of the Casimir effect is that the anharmonicity of the Casimir potential becomes significant when the separation of microscale objects is in the sub-100nm regime. This regime is readily accessible by many of the realized gradient-force-based optomechanical structures. Hence, a new avenue of probing the Casimir effect on-chip all-optically has become available. We propose an integrated optomechanical platform, consisting of a suspended photonic crystal membrane evanescently coupled with a silicon-on-insulator substrate, for (i) measuring the Casimir force gradient and (ii) counteracting the attractive force by exerting a resonantly enhanced repulsive optical gradient force. This thesis first presents the full characterization of the optomechanical properties of the system in vacuo. The interplay of the optical gradient force (optomechanical coupling strength \(g_{om}/2\pi=- 66GHz/nm\)) and the photothermal force manifested in the optical spring effect and dynamic backaction is elucidated. Static displacement by the repulsive force of 1nm/mW is also demonstrated.
In the second part of the thesis, the nonlinear mechanical signatures upon a strong coherent drive are reported. By resonantly driving the photonic crystal membrane with a piezo-actuator and an optical gradient force, we observed mechanical frequency mixing, mechanical bistability and non-trivial interactions of the Brownian peak with the driving signal. Finally we present our recent progress in establishing electro- static control of individual photonic crystal membranes to reduce and calibrate the electrostatic artifact which plagues Casimir measurements.
The results discussed in this thesis point towards an auspicious future of a complete realization of a Casimir optomechanical structure and novel applications with nonlinearity afforded by the Casimir force and the optical gradient force. / Engineering and Applied Sciences
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Nano-scale temperature dependent visco-elastic properties of polyethylene terephthalate (PET) using atomic force microscope (AFM).Grant, Colin, A., Alfouzan, Abdulrahman, Twigg, Peter C., Coates, Philip D., Gough, Timothy D. 2012 June 1920 (has links)
Visco-elastic behaviour at the nano-level of a commonly used polymer (PET) is characterised using atomic force microscopy (AFM) at a range of temperatures. The modulus, indentation creep and relaxation time of the PET film (thickness = 100 m) is highly sensitive to temperature over an experimental temperature range of 22¿175 ¿C. The analysis showed a 40-fold increase in the amount of indentation creep on raising the temperature from 22 ¿C to 100 ¿C, with the most rapid rise occurring above the glass-to-rubber transition temperature (Tg = 77.1 ¿C). At higher temperatures, close to the crystallisation temperature (Tc = 134.7 ¿C), the indentation creep reduced to levels similar to those at temperatures below Tg. The calculated relaxation time showed a similar temperature dependence, rising from 0.6 s below Tg to 1.2 s between Tg and Tc and falling back to 0.6 s above Tc. Whereas, the recorded modulus of the thick polymer film decreases above Tg, subsequently increasing near Tc. These visco-elastic parameters are obtained via mechanical modelling of the creep curves and are correlated to the thermal phase changes that occur in PET, as revealed by differential scanning calorimetry (DSC).
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