1,610 research outputs found
CAPTCHaStar! A novel CAPTCHA based on interactive shape discovery
Over the last years, most websites on which users can register (e.g., email
providers and social networks) adopted CAPTCHAs (Completely Automated Public
Turing test to tell Computers and Humans Apart) as a countermeasure against
automated attacks. The battle of wits between designers and attackers of
CAPTCHAs led to current ones being annoying and hard to solve for users, while
still being vulnerable to automated attacks.
In this paper, we propose CAPTCHaStar, a new image-based CAPTCHA that relies
on user interaction. This novel CAPTCHA leverages the innate human ability to
recognize shapes in a confused environment. We assess the effectiveness of our
proposal for the two key aspects for CAPTCHAs, i.e., usability, and resiliency
to automated attacks. In particular, we evaluated the usability, carrying out a
thorough user study, and we tested the resiliency of our proposal against
several types of automated attacks: traditional ones; designed ad-hoc for our
proposal; and based on machine learning. Compared to the state of the art, our
proposal is more user friendly (e.g., only some 35% of the users prefer current
solutions, such as text-based CAPTCHAs) and more resilient to automated
attacks.Comment: 15 page
Effect of liquid spreading due to nano/microstructures on the critical heat flux during pool boiling
It is well known that nanoparticles deposited on a heating surface during nanofluid boiling can change the characteristics of the heating surface and increase the critical heat flux (CHF) dramatically. We considered a new approach to investigate the nanoparticle surface effect on CHF enhancement using surfaces modified with artificial micro/nanostructures similar to deposited nanoparticle structures. We examined the effect of the surface wettability and liquid spreading ability on the CHF. The results demonstrated that the CHF enhancement on the modified surfaces was a consequence of both the improved surface wettability and the liquid spreading ability of the artificial micro/nanostructures. © 2011 American Institute of Physics.open11102116Nsciescopu
RNAi: An emerging field of molecular research
RNA silencing, named as co-suppression or post transcriptional gene silencing (PTGS) was found in transgenic plants which was the result of cellular mRNA degradation and silencing of gene expression.RNA interference (RNAi) is a specific technique using only a few double stranded RNA (dsRNA) molecules to stop the expression which has made it one of the important areas in molecular biology. By introducing a gene into the host genome which is highly homologous to an endogenous gene, the RNA silencing is initiated. Double-stranded RNA (dsRNA) is cut by the enzyme “Dicer” producing small interfering RNAs (siRNAs) which combine with RNA-induced silencing complex (RISC). RISC, a protein complex, binds one strand of siRNA with mRNA of native target gene for destruction, resulting in gene silencing. The mechanism of RNAi offers a quick and easy way to determine the function of a gene. In this review, we discuss the history, components, mechanism and the application of RNA interference
Large-Theta(13) Perturbation Theory of Neutrino Oscillation for Long-Baseline Experiments
The Cervera et al. formula, the best known approximate formula of neutrino
oscillation probability for long-baseline experiments, can be regarded as a
second-order perturbative formula with small expansion parameter epsilon \equiv
Delta m^2_{21} / Delta m^2_{31} \simeq 0.03 under the assumption s_{13} \simeq
epsilon. If theta_{13} is large, as suggested by a candidate nu_{e} event at
T2K as well as the recent global analyses, higher order corrections of s_{13}
to the formula would be needed for better accuracy. We compute the corrections
systematically by formulating a perturbative framework by taking theta_{13} as
s_{13} \sim \sqrt{epsilon} \simeq 0.18, which guarantees its validity in a wide
range of theta_{13} below the Chooz limit. We show on general ground that the
correction terms must be of order epsilon^2. Yet, they nicely fill the mismatch
between the approximate and the exact formulas at low energies and relatively
long baselines. General theorems are derived which serve for better
understanding of delta-dependence of the oscillation probability. Some
interesting implications of the large theta_{13} hypothesis are discussed.Comment: Fig.2 added, 23 pages. Matches to the published versio
Moxifloxacin: Clinically compatible contrast agent for multiphoton imaging
Multiphoton microscopy (MPM) is a nonlinear fluorescence microscopic technique widely used for cellular imaging of thick tissues and live animals in biological studies. However, MPM application to human tissues is limited by weak endogenous fluorescence in tissue and cytotoxicity of exogenous probes. Herein, we describe the applications of moxifloxacin, an FDA-approved antibiotic, as a cell-labeling agent for MPM. Moxifloxacin has bright intrinsic multiphoton fluorescence, good tissue penetration and high intracellular concentration. MPM with moxifloxacin was demonstrated in various cell lines, and animal tissues of cornea, skin, small intestine and bladder. Clinical application is promising since imaging based on moxifloxacin labeling could be 10 times faster than imaging based on endogenous fluorescence.1152sciescopu
Thermoelectric materials by using two-dimensional materials with negative correlation between electrical and thermal conductivity
In general, in thermoelectric materials the electrical conductivity sigma and thermal conductivity kappa are related and thus cannot be controlled independently. Previously, to maximize the thermoelectric figure of merit in state-of-the-art materials, differences in relative scaling between sigma and kappa as dimensions are reduced to approach the nanoscale were utilized. Here we present an approach to thermoelectric materials using tin disulfide, SnS2, nanosheets that demonstrated a negative correlation between sigma and kappa. In other words, as the thickness of SnS2 decreased, sigma increased whereas kappa decreased. This approach leads to a thermoelectric figure of merit increase to 0.13 at 300 K, a factor similar to 1,000 times greater than previously reported bulk single-crystal SnS2. The Seebeck coefficient obtained for our two-dimensional SnS2 nanosheets was 34.7mVK(-1) for 16-nm-thick samples at 300 K.114330Ysciescopu
Evolutionary Toggling of Vpx/Vpr Specificity Results in Divergent Recognition of the Restriction Factor SAMHD1
SAMHD1 is a host restriction factor that blocks the ability of lentiviruses such as HIV-1 to undergo reverse transcription in myeloid cells and resting T-cells. This restriction is alleviated by expression of the lentiviral accessory proteins Vpx and Vpr (Vpx/Vpr), which target SAMHD1 for proteasome-mediated degradation. However, the precise determinants within SAMHD1 for recognition by Vpx/Vpr remain unclear. Here we show that evolution of Vpx/Vpr in primate lentiviruses has caused the interface between SAMHD1 and Vpx/Vpr to alter during primate lentiviral evolution. Using multiple HIV-2 and SIV Vpx proteins, we show that Vpx from the HIV-2 and SIVmac lineage, but not Vpx from the SIVmnd2 and SIVrcm lineage, require the C-terminus of SAMHD1 for interaction, ubiquitylation, and degradation. On the other hand, the N-terminus of SAMHD1 governs interactions with Vpx from SIVmnd2 and SIVrcm, but has little effect on Vpx from HIV-2 and SIVmac. Furthermore, we show here that this difference in SAMHD1 recognition is evolutionarily dynamic, with the importance of the N- and C-terminus for interaction of SAMHD1 with Vpx and Vpr toggling during lentiviral evolution. We present a model to explain how the head-to-tail conformation of SAMHD1 proteins favors toggling of the interaction sites by Vpx/Vpr during this virus-host arms race. Such drastic functional divergence within a lentiviral protein highlights a novel plasticity in the evolutionary dynamics of viral antagonists for restriction factors during lentiviral adaptation to its hosts. © 2013 Fregoso et al
Coarse-grained reconfigurable array architectures
Coarse-Grained Reconfigurable Array (CGRA) architectures accelerate the same inner loops that benefit from the high ILP support in VLIW architectures. By executing non-loop code on other cores, however, CGRAs can focus on such loops to execute them more efficiently. This chapter discusses the basic principles of CGRAs, and the wide range of design options available to a CGRA designer, covering a large number of existing CGRA designs. The impact of different options on flexibility, performance, and power-efficiency is discussed, as well as the need for compiler support. The ADRES CGRA design template is studied in more detail as a use case to illustrate the need for design space exploration, for compiler support and for the manual fine-tuning of source code
The Epstein-Barr Virus G-Protein-Coupled Receptor Contributes to Immune Evasion by Targeting MHC Class I Molecules for Degradation
Epstein-Barr virus (EBV) is a human herpesvirus that persists as a largely subclinical infection in the vast majority of adults worldwide. Recent evidence indicates that an important component of the persistence strategy involves active interference with the MHC class I antigen processing pathway during the lytic replication cycle. We have now identified a novel role for the lytic cycle gene, BILF1, which encodes a glycoprotein with the properties of a constitutive signaling G-protein-coupled receptor (GPCR). BILF1 reduced the levels of MHC class I at the cell surface and inhibited CD8+ T cell recognition of
endogenous target antigens. The underlying mechanism involves physical association of BILF1 with MHC class I molecules, an increased turnover from the cell surface, and enhanced degradation via lysosomal proteases. The BILF1 protein of the closely related CeHV15 c1-herpesvirus of the Rhesus Old World primate (80% amino acid sequence identity) downregulated surface MHC class I similarly to EBV BILF1. Amongst the human herpesviruses, the GPCR encoded by the ORF74 of the KSHV c2-herpesvirus is most closely related to EBV BILF1 (15% amino acid sequence identity) but did not affect levels of surface MHC class I. An engineered mutant of BILF1 that was unable to activate G protein signaling pathways retained the ability to downregulate MHC class I, indicating that the immune-modulating and GPCR-signaling properties are two distinct functions of BILF1. These findings extend our understanding of the normal biology of an important human pathogen. The discovery of a third EBV lytic cycle gene that cooperates to interfere with MHC class I antigen processing underscores the importance of the need for EBV to be able to evade CD8+ T cell responses during the lytic replication cycle, at a time when such a large number of potential viral targets are expressed
Loss of superhydrophobicity of hydrophobic micro/nano structures during condensation
Condensed liquid behavior on hydrophobic micro/nano-structured surfaces is a subject with multiple practical applications, but remains poorly understood. In particular, the loss of superhydrophobicity of hydrophobic micro/nanostructures during condensation, even when the same surface shows water-repellant characteristics when exposed to air, requires intensive investigation to improve and apply our understanding of the fundamental physics of condensation. Here, we postulate the criterion required for condensation to form from inside the surface structures by examining the grand potentials of a condensation system, including the properties of the condensed liquid and the conditions required for condensation. The results imply that the same hydrophobic micro/nano-structured surface could exhibit different liquid droplet behavior depending on the conditions. Our findings are supported by the observed phenomena: the initiation of a condensed droplet from inside a hydrophobic cavity, the apparent wetted state changes, and the presence of sticky condensed droplets on the hydrophobic micro/nano-structured surface. © 2015, Macmillan Publishers Limited. All rights reserved.open111616Nsciescopu
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