Liposome-cell interaction: transfer and intracellular release of a trapped fluorescent marker

When small, unilamellar lipid vesicles containing a high concentration of the fluorescent dye 6-carboxyfluorescein are incubated with either frog retinas or human lymphocytes, fluroescence distributes widely throughout each cell. Since "self-quenching" largely prevents the dye from fluorescing as long as it remains sequestered in vesicles, it is clear that a considerable amount of dye is released from the vesicles and diluted into the much larger volume of the cell.     

The IEEE P1520 standards initiative for programmable networkinterfaces

This article discusses the need for standard software interfaces for programming of networks, specifically for service and signaling control, through programming interfaces. The objective is to enable the development of open signaling, control, and management applications as well as higher-level multimedia services on networks. The scope of this effort includes ATM switches, circuit switches, IP routers, and hybrid switches such as those that provide for fast switching of IP packets over an ATM backbone. The basic ideas represented herein are in the process of development as a standard for application programming interfaces for networks under IEEE Standards Project IEEE P1520     

New criteria for blind deconvolution of nonminimum phase systems(channels)

A necessary and sufficient condition for blind deconvolution (without observing the input) of nonminimum-phase linear time-invariant systems (channels) is derived. Based on this condition, several optimization criteria are proposed, and their solution is shown to correspond to the desired response. These criteria involve the computation only of second- and fourth-order moments, implying a simple tap update procedure. The proposed methods are universal in the sense that they do not impose any restrictions on the probability distribution of the (unobserved) input sequence. It is shown that in several important cases (e.g. when the additive noise is Gaussian), the proposed criteria are essentially unaffected     

On the reassessment of doses in TL-dosimetry by measuring the residual dose

Second readouts and the photo-transferred thermoluminscence (PTTL) method are sometimes used to reassess high doses. When using the common LiF:Mg,Ti, if the second readout is performed by a regular readout cycle of 13.3 s, its efficiency is low and the estimations cannot be obtained with acceptable accuracy for low doses in the 10-100 mSv range. By applying the PTTL method, the efficiency is much higher, but a high background is also present, deteriorating the quality of the reassessment. A simple and efficient method was studied, which consists of expanding the heating time to 30 s. Although the efficiency relative to a standard readout is improved by only a factor of 3, the low background enables to obtain results with the same uncertainty as the more complicated PTTL method. By applying region of integration discrimination, the errors can be further diminished.     

On the reassessment of thermal neutron doses in TLD-100 by measuring the residual dose

By employing second readouts and the Phototransferred thermoluminescence (PTTL) method, high doses may be reassessed on the basis of residual dose information. It was shown in the past that for TLD-100, gamma doses can be reassessed by using a simple and efficient method, which consists of expanding the heating time to 30 s. In the present study, the 'extended time' method and the PTTL residual dose evaluations are used for reassessing thermal neutron doses when using TLD-100 crystals. Reassessment characteristics are presented for relatively low thermal neutron doses, in the range between approximately 1 and 18 mSv gamma dose equivalent.     

Intercellular junctions in FANFT-induced carcinomas of rat urinary bladder in tissue culture: in situ thin-section, freeze-fracture, and scanning electron microscopy studies.

This paper describes a set of simple methods for comparative light and electron microscopy studies on tissue cultured tumour cells derived from both noninvasive and invasive carcinogen-induced rat urinary bladder carcinomas. Cells are grown on Thermanox plastic coverslips and fixed in situ. Each plastic coverslip is then divided with scissors into four parts: the first is processed for light microscopy, the second for thin-section electron microscopy, the third for freeze-fracture electron microscopy, and the fourth for scanning electron microscopy. In some experiments, portions of the culture which have first been examined by light microscopy are subsequently prepared for electron microscopy. In this way, the culture conditions are kept constant and comparison of structural features (i.e. intercellular junctions) by several preparative techniques is possible. Noninvasive and invasive rat bladder tumour cells, characterized by numerous pleomorphic microvilli, have normal zonulae occludentes at the apices of lateral surfaces of tumour cells in all cultures. In some areas of invasive tumour cells, occludens junctions are focally attenuated, consisting of only one or two strands, and occasionally the strands are discontinuous. Gap junctions, type PF-1, as well as numerous demosomes are present in all cell lines. Thus, intercellular junctions in noninvasive and invasive rate bladder epithelial cell lines bear a striking resemblance to those previously described in the comparable solid primary tumours. These culture systems may be useful for studying factors which influence the formation of intercellular junctions during malignant transformation.     

MHD flow of a micropolar fluid towards a vertical permeable plate with prescribed surface heat flux

The problem of a steady mixed convection stagnation point flow towards a permeable vertical plate with prescribed surface heat flux immersed in an incompressible micropolar fluid is studied numerically. The governing partial differential equations are first transformed into a system of ordinary differential equations using a similarity transformation, before being solved numerically by a finite-difference scheme known as the Keller-box method and the Runge–Kutta–Fehlberg method with shooting technique. The effects of the material parameter, buoyancy parameter, suction/injection parameter and the Prandtl number on the fluid flow and heat transfer characteristics are discussed. It is found that dual solutions exist for both assisting and opposing flows. The skin friction coefficient and the local Nusselt number increase in the presence of suction and magnetic field. Moreover, suction as well as fluids with larger Prandtl number widens the range of the buoyancy parameter for which the solution exists.     

Genes Involved in the Endoplasmic Reticulum N-Glycosylation Pathway of the Red Microalga Porphyridium sp.: A Bioinformatic Study

N-glycosylation is one of the most important post-translational modifications that influence protein polymorphism, including protein structures and their functions. Although this important biological process has been extensively studied in mammals, only limited knowledge exists regarding glycosylation in algae. The current research is focused on the red microalga Porphyridium sp., which is a potentially valuable source for various applications, such as skin therapy, food, and pharmaceuticals. The enzymes involved in the biosynthesis and processing of N-glycans remain undefined in this species, and the mechanism(s) of their genetic regulation is completely unknown. In this study, we describe our pioneering attempt to understand the endoplasmic reticulum N-Glycosylation pathway in Porphyridium sp., using a bioinformatic approach. Homology searches, based on sequence similarities with genes encoding proteins involved in the ER N-glycosylation pathway (including their conserved parts) were conducted using the TBLASTN function on the algae DNA scaffold contigs database. This approach led to the identification of 24 encoded-genes implicated with the ER N-glycosylation pathway in Porphyridium sp. Homologs were found for almost all known N-glycosylation protein sequences in the ER pathway of Porphyridium sp.; thus, suggesting that the ER-pathway is conserved; as it is in other organisms (animals, plants, yeasts, etc.).     

Selective decomposition of isopropanol using as prepared and oxidized graphite nanofibers

Three types of as prepared and treated graphite nanofibers (GNFs) were used as catalysts in the decomposition of isopropanol to propene and acetone in the presence of oxygen to evaluate the surface chemistry of the fibers. As prepared herringbone fibers were found to produce higher selectivity for propene compared to the as prepared platelet and ribbon fibers at all temperatures explored. Herringbone fibers that had undergone oxidative treatment with nitric acid, phosphoric acid, ruthenium tetroxide or potassium permanganate were also evaluated at a 290 °C. Effects of oxidation treatments on fiber structure were evaluated using a host of analytical techniques including BET, SEM/EDS, TGA, XPS, and fluorescence labeling of surface species. Selectivity for acetone dehydrogenation product or propene dehydration product could be achieved by the appropriate surface treatment. Nitric acid was the mildest treatment and the treated fibers showed minimal changes. (Potassium permanganate was a harsh treatment that almost completely degraded fiber structure, creating amorphous carbon.) Phosphoric acid treated fibers were found to produce very high conversions and almost pure selectivity for propene. Ruthenium tetroxide did not appear to have a large affect on fiber morphology; however, selectivity for acetone was much higher when GNFs were treated with ruthenium tetroxide.