Correlation between Leptonic CP Violation and mu-tau Symmetry Breaking

Considering the $\mu$-$\tau$ symmetry, we discuss a direct linkage between phases of flavor neutrino masses and leptonic CP violation by determining three eigenvectors associated with ${\rm\bf M}=M^\dagger_\nu M_\nu$ for a complex flavor neutrino mass matrix $M_\nu$ in the flavor basis. Since the Dirac CP violation is absent in the $\mu$-$\tau$ symmetric limit, leptonic CP violation is sensitive to the $\mu$-$\tau$ symmetry breaking, whose effect can be evaluated by perturbation. It is found that the Dirac phase ($\delta$) arises from the $\mu$-$\tau$ symmetry breaking part of ${\rm\bf M}_{e\mu,e\tau}$ and an additional phase ($\rho$) is associated with the $\mu$-$\tau$ symmetric part of ${\rm\bf M}_{e\mu,e\tau}$, where ${\rm\bf M}_{ij}$ stands for an $ij$ matrix element ($i,j$=$e,\mu,\tau$). The phase $\rho$ is redundant and can be removed but leaves its effect in the Dirac CP violation characterized by $\sin (\delta + \rho)$. The perturbative results suggest the exact formula of mixing parameters including that of $\delta$ and $\rho$, which turns out to be free from the effects of the redundant phases. As a result, it is generally shown that the maximal atmospheric neutrino mixing necessarily accompanies either $\sin\theta_{13}=0$ or $\cos(\delta+\rho)=0$, the latter of which indicates maximal CP violation, where $\theta_{13}$ is the $\nu_e$-$\nu_\tau$ mixing angle.Comment: 16 pages, ReVTeX, references updated, typos corredcted, published version in Physical Reviews

Two Categories of Approximately mu-tau Symmetric Neutrino Mass Textures

Our approximately \mu-\tau symmetric neutrino mass textures fall into two different categories, whose behaviors in the \mu-\tau symmetric limit are characterized by either \sin(theta_{13})->0 (referred to as C1)), or \sin(theta_{12})->0 (referred to as C2)). We present ten phenomenologically viable neutrino mass textures: two for the normal mass hierarchy, three for the inverted mass hierarchy, and five for the quasi degenerate mass pattern. Tiny \mu-\tau symmetry breaking ensures that \sin^2(theta_{13}) << 1 for C1), and \Delta m^2_\odot/\Delta m^2_{atm} (\equiv R) << 1 for C2). A correlation among small quantities is provided by \cos 2(theta_{23}) \sim \sin(theta_{13}) for C1), and by either \cos(2theta_{23}) \sim R, or \cos(2theta_{23})\sin(theta_{13}) \sim R for C2). It is further shown that \tan(2theta_{12}) \sim \cos(2theta_{23})/\sin(theta_{13}) is satisfied for C2). We find specific properties for each mass ordering, which are discussed in this article.Comment: 31 pages, 15 figures (High-resolution figures can be downloaded from http://www.sp.u-tokai.ac.jp/~yasue/two_categories_of.pdf.tar.gz

Improved Network Performance via Antagonism: From Synthetic Rescues to Multi-drug Combinations

Recent research shows that a faulty or sub-optimally operating metabolic network can often be rescued by the targeted removal of enzyme-coding genes--the exact opposite of what traditional gene therapy would suggest. Predictions go as far as to assert that certain gene knockouts can restore the growth of otherwise nonviable gene-deficient cells. Many questions follow from this discovery: What are the underlying mechanisms? How generalizable is this effect? What are the potential applications? Here, I will approach these questions from the perspective of compensatory perturbations on networks. Relations will be drawn between such synthetic rescues and naturally occurring cascades of reaction inactivation, as well as their analogues in physical and other biological networks. I will specially discuss how rescue interactions can lead to the rational design of antagonistic drug combinations that select against resistance and how they can illuminate medical research on cancer, antibiotics, and metabolic diseases.Comment: Online Open "Problems and Paradigms" articl

Cellulose acetate phthalate, a common pharmaceutical excipient, inactivates HIV-1 and blocks the coreceptor binding site on the virus envelope glycoprotein gp120

BACKGROUND: Cellulose acetate phthalate (CAP), a pharmaceutical excipient used for enteric film coating of capsules and tablets, was shown to inhibit infection by the human immunodeficiency virus type 1 (HIV-1) and several herpesviruses. CAP formulations inactivated HIV-1, herpesvirus types 1 (HSV-1) and 2 (HSV-2) and the major nonviral sexually transmitted disease (STD) pathogens and were effective in animal models for vaginal infection by HSV-2 and simian immunodeficiency virus. METHODS: Enzyme-linked immunoassays and flow cytometry were used to demonstrate CAP binding to HIV-1 and to define the binding site on the virus envelope. RESULTS: 1) CAP binds to HIV-1 virus particles and to the envelope glycoprotein gp120; 2) this leads to blockade of the gp120 V3 loop and other gp120 sites resulting in diminished reactivity with HIV-1 coreceptors CXCR4 and CCR5; 3) CAP binding to HIV-1 virions impairs their infectivity; 4) these findings apply to both HIV-1 IIIB, an X4 virus, and HIV-1 BaL, an R5 virus. CONCLUSIONS: These results provide support for consideration of CAP as a topical microbicide of choice for prevention of STDs, including HIV-1 infection

Intermittent maser flare around the high mass young stellar object G353.273+0.641 I: data & overview

We have performed VLBI and single-dish monitoring of 22 GHz H$_{2}$O maser emission from the high mass young stellar object G353.273+0.641 with VERA (VLBI Exploration of Radio Astrometry) and Tomakamai 11-m radio telescope. Two maser flares have been detected, separated almost two years. Frequent VLBI monitoring has revealed that these flare activities have been accompanied by structural change of the prominent shock front traced by H2O maser alignments. We have detected only blue-shifted emissions and all maser features have been distributed within very small area of 200 $\times$ 200 au$^{2}$ in spite of wide velocity range (> 100 km s$^{-1}$). The light curve shows notably intermittent variation and suggests that the H$_{2}$O masers in G353.273+0.641 are excited by episodic radio jet. The time-scale of \sim2 yr and characteristic velocity of \sim500 km s$^{-1}$ also support this interpretation. Two isolated velocity components of C50 (-53 \pm 7 km s$^{-1}$) and C70 (-73 \pm 7 km s$^{-1}$) have shown synchronised linear acceleration of the flux weighted V_{\rmn{LSR}} values (\sim-5 km s$^{-1}$ yr$^{-1}$) during the flare phase. This can be converted to the lower-limit momentum rate of 1.1 \times 10$^{-3}$ M_{\sun} km s$^{-1}$ yr$^{-1}$. Maser properties are quite similar to that of IRAS 20126+4104 especially. This corroborates the previous suggestion that G353.273+0.641 is a candidate of high mass protostellar object. The possible pole-on geometry of disc-jet system can be suitable for direct imaging of the accretion disc in this case.Comment: 13 pages, 5 figures accepted for publication in MNRA

Leptogenesis and dark matter unified in a non-SUSY model for neutrino masses

We propose a unified explanation for the origin of dark matter and baryon number asymmetry on the basis of a non-supersymmetric model for neutrino masses. Neutrino masses are generated in two distinct ways, that is, a tree-level seesaw mechanism with a single right-handed neutrino, and one-loop radiative effects by a new additional doublet scalar. A spontaneously broken U(1)$^\prime$ brings a $Z_2$ symmetry which restricts couplings of this new scalar and controls the neutrino masses. It also guarantees the stability of a CDM candidate. We examine two possible candidate for the CDM. We also show that the decay of a heavy right-handed neutrino related to the seesaw mechanism can generate baryon number asymmetry through leptogenesis.Comment: 21 pages, 3 figures, extended version for publication, references adde

Effects of the terms associated with phi(zz) in free surface condition on the attitudes and resistance of different ships

One of approaches for numerical simulation of a ship moving in a still water is based on the composition of double-body flow and wavy flow solved by a boundary element method. There are several terms related to the second order derivative (ϕzz) of double-body flow velocity potential with respect to the vertical coordinate in the free surface conditions. Understanding of the effects of the terms is very limited so far. In many cases, they are just ignored even for ships with a high forward speed, particularly in the cases associated with multihull ships, for which no investigations on their effects have been found. This paper will present a study on the effects of the terms on the numerical prediction of the attitudes and resistance of different ships in various situations, including monohull, catamaran and trimaran with different parameters and at different Froude numbers. The results will demonstrate that the effects of the terms are significant in many cases and that considering this term may lead to the results similar to those obtained by fully nonlinear models at high Froude numbers

Expression of aldehyde dehydrogenase and CD133 defines ovarian cancer stem cells

Identification of cancer stem cells is crucial for advancing cancer biology and therapy. Several markers including CD24, CD44, CD117, CD133, the G subfamily of ATP‐binding cassette transporters (ABCG), epithelial specific antigen (ESA) and aldehyde dehydrogenase (ALDH) are used to identify and investigate human epithelial cancer stem cells in the literature. We have now systemically analyzed and compared the expression of these markers in fresh ovarian epithelial carcinomas. Although the expression levels of these markers were unexpectedly variable and partially overlapping in fresh ovarian cancer cells from different donors, we reliably detected important levels of CD133 and ALDH in the majority of fresh ovarian cancer. Furthermore, most of these stem cell markers including CD133 and ALDH were gradually lost following in vitro passage of primary tumor cells. However, the expression of ALDH and CD133, but not CD24, CD44 and CD117, could be partially rescued by the in vitro serum‐free and sphere cultures and by the in vivo passage in the immune‐deficient xenografts. ALDH + and CD133 + cells formed three‐dimensional spheres more efficiently than their negative counterparts. These sphere‐forming cells expressed high levels of stem cell core gene transcripts and could be expanded and form additional spheres in long‐term culture. ALDH + , CD133 + and ALDH + CD133 + cells from fresh tumors developed larger tumors more rapidly than their negative counterparts. This property was preserved in the xenografted tumors. Altogether, the data suggest that ALDH + and CD133 + cells are enriched with ovarian cancer‐initiating (stem) cells and that ALDH and CD133 may be widely used as reliable markers to investigate ovarian cancer stem cell biology.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/88104/1/25967_ftp.pd

Export of functional Streptomyces coelicolor alditol oxidase to the periplasm or cell surface of Escherichia coli and its application in whole-cell biocatalysis

Streptomyces coelicolor A3(2) alditol oxidase (AldO) is a soluble monomeric flavoprotein in which the flavin cofactor is covalently linked to the polypeptide chain. AldO displays high reactivity towards different polyols such as xylitol and sorbitol. These characteristics make AldO industrially relevant, but full biotechnological exploitation of this enzyme is at present restricted by laborious and costly purification steps. To eliminate the need for enzyme purification, this study describes a whole-cell AldO biocatalyst system. To this end, we have directed AldO to the periplasm or cell surface of Escherichia coli. For periplasmic export, AldO was fused to endogenous E. coli signal sequences known to direct their passenger proteins into the SecB, signal recognition particle (SRP), or Twin-arginine translocation (Tat) pathway. In addition, AldO was fused to an ice nucleation protein (INP)-based anchoring motif for surface display. The results show that Tat-exported AldO and INP-surface-displayed AldO are active. The Tat-based system was successfully employed in converting xylitol by whole cells, whereas the use of the INP-based system was most likely restricted by lipopolysaccharide LPS in wild-type cells. It is anticipated that these whole-cell systems will be a valuable tool for further biological and industrial exploitation of AldO and other cofactor-containing enzymes.