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Fibre Assembly (fibre + assembly)

Distribution by Scientific Domains

Medical Sciences	75%

Selected Abstracts

Automation of solid-phase microextraction

JOURNAL OF SEPARATION SCIENCE, JSS, Issue 15 2005
John O'Reilly
Abstract This review discusses developments and future challenges in the automation of solid-phase microextraction (SPME). The emphasis of the review is placed on automated SPME-GC using fibre and in-tube configurations, and includes discussion of recent developments that may have significant implications for automation such as superelastic fibre assemblies and internally cooled fibre-SPME. Existing methods used for automated SPME-LC are summarised together with a more detailed overview of recent developments such as using solvent desorption followed by syringe injection using a robotic system. Progress towards automation of other SPME configurations is also discussed. [source]

Mechanisms of actin stress fibre assembly

JOURNAL OF MICROSCOPY, Issue 3 2008
P. NAUMANEN
Summary Stress fibres are contractile acto-myosin structures found from many types of non-muscle cells, where they are involved in adhesion, motility and morphogenesis. Stress fibres typically display a periodic ,-actinin,myosin II pattern and are thus suggested to resemble the sarcomeric actin filament structures of muscle cells. Mammalian cells contain three categories of stress fibres: ventral stress fibres that are attached to focal adhesions at both ends, dorsal stress fibres that are attached to focal adhesions typically at one end and transverse arcs that are curved acto-myosin bundles, which do not directly attach to focal adhesions. In this review, we discuss the definition of stress fibres, organization of actin filaments and other components within these contractile structures, and the mechanisms of stress fibre assembly. [source]

Role of dystrophins and utrophins in platelet adhesion process

BRITISH JOURNAL OF HAEMATOLOGY, Issue 1 2006
Doris Cerecedo
Summary Platelets are crucial at the site of vascular injury, adhering to the sub-endothelial matrix through receptors on their surface, leading to cell activation and aggregation to form a haemostatic plug. Platelets display focal adhesions as well as stress fibres to contract and facilitate expulsion of growth and pro-coagulant factors contained in the granules and to constrict the clot. The interaction of F-actin with different actin-binding proteins determines the properties and composition of the focal adhesions. Recently, we demonstrated the presence of dystrophin-associated protein complex corresponding to short dystrophin isoforms (Dp71d and Dp71) and the uthophin gene family (Up400 and Up71), which promote shape change, adhesion, aggregation, and granule centralisation. To elucidate participation of both complexes during the platelet adhesion process, their potential association with integrin , -1 fraction and the focal adhesion system (, -actinin, vinculin and talin) was evaluated by immunofluorescence and immunoprecipitation assays. It was shown that the short dystrophin-associated protein complex participated in stress fibre assembly and in centralisation of cytoplasmic granules, while the utrophin-associated protein complex assembled and regulated focal adhesions. The simultaneous presence of dystrophin and utrophin complexes indicates complementary structural and signalling mechanisms to the actin network, improving the platelet haemostatic role. [source]