444 research outputs found
Plane Formation by Synchronous Mobile Robots in the Three Dimensional Euclidean Space
Creating a swarm of mobile computing entities frequently called robots,
agents or sensor nodes, with self-organization ability is a contemporary
challenge in distributed computing. Motivated by this, we investigate the plane
formation problem that requires a swarm of robots moving in the three
dimensional Euclidean space to land on a common plane. The robots are fully
synchronous and endowed with visual perception. But they do not have
identifiers, nor access to the global coordinate system, nor any means of
explicit communication with each other. Though there are plenty of results on
the agreement problem for robots in the two dimensional plane, for example, the
point formation problem, the pattern formation problem, and so on, this is the
first result for robots in the three dimensional space. This paper presents a
necessary and sufficient condition for fully-synchronous robots to solve the
plane formation problem that does not depend on obliviousness i.e., the
availability of local memory at robots. An implication of the result is
somewhat counter-intuitive: The robots cannot form a plane from most of the
semi-regular polyhedra, while they can form a plane from every regular
polyhedron (except a regular icosahedron), whose symmetry is usually considered
to be higher than any semi-regular polyhedrdon
Characterization of the binding of botulinum type B 16S toxin to human intestinal epithelial cells
Botulinum neurotoxin produced by Clostridium botulinum type B is a complex of 12S and 16S toxins. 12S toxin consists of a neurotoxin and a nontoxic non-HA (NTNH). The 16S toxin consists of a neurotoxin, an NTNH, and a hemagglutinin (HA). Food-borne botulism is caused by these complex toxins, which are ingested orally and absorbed from the digestive tract across the epithelial barrier lining the gut.
Here we show that the type B 16S toxin, but not the 12S toxin or the neurotoxin, binds to the T84 human intestinal epithelial cell line. We also demonstrate that the HA moiety in the 16S toxin mediates the toxin binding to the cells. The carbohydrates containing a galactose moiety inhibited the binding of the 16S toxin to the T84 cells, and neuraminidase treatment of the cells increased the 16S toxin binding. The binding of the 16S toxin to the neuraminidase-treated cells was also inhibited by carbohydrates containing a galactose moiety. These results suggest that the type B 16S toxin binds to human intestinal epithelial cells via the galactose moiety in the carbohydrate chain on the cell surface
Exploration of Finite 2D Square Grid by a Metamorphic Robotic System
We consider exploration of finite 2D square grid by a metamorphic robotic
system consisting of anonymous oblivious modules. The number of possible shapes
of a metamorphic robotic system grows as the number of modules increases. The
shape of the system serves as its memory and shows its functionality. We
consider the effect of global compass on the minimum number of modules
necessary to explore a finite 2D square grid. We show that if the modules agree
on the directions (north, south, east, and west), three modules are necessary
and sufficient for exploration from an arbitrary initial configuration,
otherwise five modules are necessary and sufficient for restricted initial
configurations
Auxiliary-level-assisted operations with charge qubits in semiconductors
We present a new scheme for rotations of a charge qubit associated with a
singly ionized pair of donor atoms in a semiconductor host. The logical states
of such a qubit proposed recently by Hollenberg et al. are defined by the
lowest two energy states of the remaining valence electron localized around one
or another donor. We show that an electron located initially at one donor site
can be transferred to another donor site via an auxiliary molecular level
formed upon the hybridization of the excited states of two donors. The electron
transfer is driven by a single resonant microwave pulse in the case that the
energies of the lowest donor states coincide or two resonant pulses in the case
that they differ from each other. Depending on the pulse parameters, various
one-qubit operations, including the phase gate, the NOT gate, and the Hadamard
gate, can be realized in short times. Decoherence of an electron due to the
interaction with acoustic phonons is analyzed and shown to be weak enough for
coherent qubit manipulation being possible, at least in the proof-of-principle
experiments on one-qubit devices.Comment: Extended version of cond-mat/0411605 with detailed discussion of
phonon-induced decoherence including dephasing and relaxation; to be
published in JET
Pattern formation
The Pattern Formation problem is one of the most important coordination problem for robotic systems. Initially the entities are in arbitrary positions; within finite time they must arrange themselves in the space so to form a pattern given in input. In this chapter, we will mainly deal with the problem in the OBLOT model
Diffusion-Weighted Imaging and Diffusion Tensor Imaging of Asymptomatic Lumbar Disc Herniation
Diffusion-weighted imaging (DWI) and diffusion tensor imaging (DTI) were performed
on a healthy 31-year-old man with asymptomatic lumbar disc herniation. Although
the left S1 nerve root was obviously entrapped by a herniated mass, neither DWI nor DTI showed any significant findings for the nerve root. Decreased apparent diffusion coefficient (ADC) values and increased fractional anisotropy (FA) values were found. These results are contrary to those in previously published studies of symptomatic patients, in which a combination of increased ADC and decreased FA seem to have a relationship with nerve injury and subsequent symptoms, such as leg pain or palsy. Our results seen in an asymptomatic subject suggest that the compressed nerve with no injury, such as edema, demyelination, or persistent axonal injury, may be indicated by a combination of decreased ADC and increased FA. ADC and FA could therefore be potential tools to elucidate the pathomechanism of radiculopathy
Gas phase characterization of the noncovalent quaternary structure of Cholera toxin and the Cholera toxin B subunit pentamer
Cholera toxin (CTx) is an AB5 cytotonic protein that has medical relevance in cholera and as a novel mucosal adjuvant. Here, we report an analysis of the noncovalent homopentameric complex of CTx B chain (CTx B5) using electrospray ionization triple quadrupole mass spectrometry and tandem mass spectrometry and the analysis of the noncovalent hexameric holotoxin usingelectrospray ionization time-of-flight mass spectrometry over a range of pH values that correlate with those encountered by this toxin after cellular uptake. We show that noncovalent interactions within the toxin assemblies were maintained under both acidic and neutral conditions in the gas phase. However, unlike the related Escherichia coli Shiga-like toxin B5 pentamer (SLTx B), the CTx B5 pentamer was stable at low pH, indicating that additional interactions must be present within the latter. Structural comparison of the CTx B monomer interface reveals an additional α-helix that is absent in the SLTx B monomer. In silico energy calculations support interactions between this helix and the adjacent monomer. These data provide insight into the apparent stabilization of CTx B relative to SLTx B
An RNAi screen for Aire cofactors reveals a role for Hnrnpl in polymerase release and Aire-activated ectopic transcription
Aire induces the expression of a large set of autoantigen genes in the thymus, driving immunological tolerance in maturing T cells. To determine the full spectrum of molecular mechanisms underlying the Aire transactivation function, we screened an AIRE-dependent gene-expression system with a genome-scale lentiviral shRNA library, targeting factors associated with chromatin architecture/function, transcription, and mRNA processing. Fifty-one functional allies were identified, with a preponderance of factors that impact transcriptional elongation compared with initiation, in particular members of the positive transcription elongation factor b (P-TEFb) involved in the release of "paused" RNA polymerases (CCNT2 and HEXIM1); mRNA processing and polyadenylation factors were also highlighted (HNRNPL/F, SFRS1, SFRS3, and CLP1). Aire's functional allies were validated on transfected and endogenous target genes, including the generation of lentigenic knockdown (KD) mice. We uncovered the effect of the splicing factor Hnrnpl on Aire-induced transcription. Transcripts sensitive to the P-TEFb inhibitor flavopiridol were reduced by Hnrnpl knockdown in thymic epithelial cells, independently of their dependence on Aire, therefore indicating a general effect of Hnrnpl on RNA elongation. This conclusion was substantiated by demonstration of HNRNPL interactions with P-TEFb components (CDK9, CCNT2, HEXIM1, and the small 7SK RNA). Aire-containing complexes include 7SK RNA, the latter interaction disrupted by HNRNPL knockdown, suggesting that HNRNPL may partake in delivering inactive P-TEFb to Aire. Thus, these results indicate that mRNA processing factors cooperate with Aire to release stalled polymerases and to activate ectopic expression of autoantigen genes in the thymu
RNA polymerase II stalling promotes nucleosome occlusion and pTEFb recruitment to drive immortalization by Epstein-Barr virus
Epstein-Barr virus (EBV) immortalizes resting B-cells and is a key etiologic agent in the development of numerous cancers. The essential EBV-encoded protein EBNA 2 activates the viral C promoter (Cp) producing a message of ~120 kb that is differentially spliced to encode all EBNAs required for immortalization. We have previously shown that EBNA 2-activated transcription is dependent on the activity of the RNA polymerase II (pol II) C-terminal domain (CTD) kinase pTEFb (CDK9/cyclin T1). We now demonstrate that Cp, in contrast to two shorter EBNA 2-activated viral genes (LMP 1 and 2A), displays high levels of promoter-proximally stalled pol II despite being constitutively active. Consistent with pol II stalling, we detect considerable pausing complex (NELF/DSIF) association with Cp. Significantly, we observe substantial Cp-specific pTEFb recruitment that stimulates high-level pol II CTD serine 2 phosphorylation at distal regions (up to +75 kb), promoting elongation. We reveal that Cp-specific pol II accumulation is directed by DNA sequences unfavourable for nucleosome assembly that increase TBP access and pol II recruitment. Stalled pol II then maintains Cp nucleosome depletion. Our data indicate that pTEFb is recruited to Cp by the bromodomain protein Brd4, with polymerase stalling facilitating stable association of pTEFb. The Brd4 inhibitor JQ1 and the pTEFb inhibitors DRB and Flavopiridol significantly reduce Cp, but not LMP1 transcript production indicating that Brd4 and pTEFb are required for Cp transcription. Taken together our data indicate that pol II stalling at Cp promotes transcription of essential immortalizing genes during EBV infection by (i) preventing promoter-proximal nucleosome assembly and ii) necessitating the recruitment of pTEFb thereby maintaining serine 2 CTD phosphorylation at distal regions
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