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711.
Fibronectin displacement at polymer surfaces   总被引:1,自引:0,他引:1  
The interactions of fibronectin with thin polymer films are studied in displacement experiments using human serum albumin. Fibronectin adsorption and exchange on two different maleic anhydride copolymer surfaces differing in hydrophobicity and surface charge density have been analyzed by quartz crystal microbalance and laser scanning microscopy with respect to adsorbed amounts, viscoelastic properties, and conformation. Fibronectin is concluded to become attached onto hydrophilic surfaces as a "softer", less rigid protein layer, in contrast to the more rigid, densely packed layer on hydrophobic surfaces. As a result, the fibronectin conformation is more distorted on the hydrophobic substrates together with remarkably different displacement characteristics in dependence on the adsorbed fibronectin surface concentration and the displacing albumin solution concentration. While the displacement kinetic remains constant for the strongly interacting surface, an acceleration in fibronectin exchange is observed for the weakly interacting surface with increasing fibronectin coverage. For displaced amounts, no change is determined for the hydrophobic substrate, in contrast to the hydrophilic substrate with a decrease of fibronectin exchange with decreasing coverage leading finally to a constant nondisplaceable amount of adsorbed proteins. Furthermore, the variation of the albumin exchange concentration reveals a stronger dependence of the kinetic for the weakly interacting substrate with higher rates at higher albumin concentrations.  相似文献   
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The increasing demand for materials with well defined microstructure, which is accompanied by the advancing miniaturization of devices calls for physically motivated, dislocation-based continuum theories of plasticity. Only recently rigorous techniques have been developed for performing meaningful averages over systems of moving, curved dislocations, yielding evolution equations for a higher order dislocation density tensor. Our continuum dislocation theory allows for generalizing the planar system towards a three-dimensional system, where dislocations may have arbitrary orientation and curvature. With the inclusion of curvature, the theory naturally takes into account a deformation-induced increase in the overall dislocation density without having to invoke ad-hoc assumptions about dislocation sources. A numerical implementation and some benchmark tests of this continuum theory for dislocation dynamics has already been discussed in the literature. In this paper, we apply this continuum theory to composite materials, where we analyze a plastically deforming matrix with an elastic inclusion. (© 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
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During surface‐enhanced Raman scattering (SERS), molecules exhibit a significant increase in their Raman signals when attached, or in very close vicinity, to gold or silver nanostructures. This effect is exploited as the basis of a new class of optical labels. Here we demonstrate robust and sensitive SERS labels as probes for imaging live cells. These hybrid labels consist of gold nanoparticles with Rose Bengal or Crystal Violet attached as reporter molecules. These new labels are stable and nontoxic, do not suffer from photobleaching, and can be excited at any excitation wavelength, even in the near infrared. SERS labels can be detected and imaged through the specific Raman signatures of the reporters. In addition, surface‐enhanced Raman spectroscopy in the local optical fields of the gold nanoparticles also provides sensitive information on the immediate molecular environment of the label in the cell and allows imaging of the native constituents of the cell. This is demonstrated by images based on a characteristic Raman line of the reporter as well as by displaying lipids based on the SERS signal of the C H deformation/bending modes at ∼1470 cm−1. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   
716.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.  相似文献   
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