Apokamps produced by repetitive discharges in air

New experimental and computational data on apokamps produced by repetitive discharges in air, including a detailed description of the research techniques used, are presented. It has been shown that plasma bullets–streamers in apokamps at low frequencies could start not only from the bright offshoot but also directly from the discharge channel. The experimental and computational data demonstrate that the visual color of apokamp changes from blue to red as the intensity ratio of the second to the first positive nitrogen system decreases with the decreasing pressure

Development of Cysteine-Free Fluorescent Proteins for the Oxidative Environment

Molecular imaging employing fluorescent proteins has been widely used to highlight specific reactions or processes in various fields of the life sciences. Despite extensive improvements of the fluorescent tag, this technology is still limited in the study of molecular events in the extracellular milieu. This is partly due to the presence of cysteine in the fluorescent proteins. These proteins almost cotranslationally form disulfide bonded oligomers when expressed in the endoplasmic reticulum (ER). Although single molecule photobleaching analysis showed that these oligomers were not fluorescent, the fluorescent monomer form often showed aberrant behavior in folding and motion, particularly when fused to cysteine-containing cargo. Therefore we investigated whether it was possible to eliminate the cysteine without losing the brightness. By site-saturated mutagenesis, we found that the cysteine residues in fluorescent proteins could be replaced with specific alternatives while still retaining their brightness. cf(cysteine-free)SGFP2 showed significantly reduced restriction of free diffusion in the ER and marked improvement of maturation when fused to the prion protein. We further applied this approach to TagRFP family proteins and found a set of mutations that obtains the same level of brightness as the cysteine-containing proteins. The approach used in this study to generate new cysteine-free fluorescent tags should expand the application of molecular imaging to the extracellular milieu and facilitate its usage in medicine and biotechnology

A SOM-based Chan–Vese model for unsupervised image segmentation

Active Contour Models (ACMs) constitute an efficient energy-based image segmentation framework. They usually deal with the segmentation problem as an optimization problem, formulated in terms of a suitable functional, constructed in such a way that its minimum is achieved in correspondence with a contour that is a close approximation of the actual object boundary. However, for existing ACMs, handling images that contain objects characterized by many different intensities still represents a challenge. In this paper, we propose a novel ACM that combines—in a global and unsupervised way—the advantages of the Self-Organizing Map (SOM) within the level set framework of a state-of-the-art unsupervised global ACM, the Chan–Vese (C–V) model. We term our proposed model SOM-based Chan– Vese (SOMCV) active contourmodel. It works by explicitly integrating the global information coming from the weights (prototypes) of the neurons in a trained SOM to help choosing whether to shrink or expand the current contour during the optimization process, which is performed in an iterative way. The proposed model can handle images that contain objects characterized by complex intensity distributions, and is at the same time robust to the additive noise. Experimental results show the high accuracy of the segmentation results obtained by the SOMCV model on several synthetic and real images, when compared to the Chan–Vese model and other image segmentation models