Structure of Titan ’ s induced magnetosphere under varying background magnetic fi eld conditions: Survey of Cassini magnetometer data from fl ybys TA – T85

Cassini magnetic field observations between 2004 and 2012 suggest the ambient field conditions near Titan’s orbit to differ significantly from the frequently applied pre-Cassini picture (background magnetic field homogeneous and perpendicular to Titan’s orbital plane, stationary upstream conditions). In this study, we analyze the impact of these varying background field conditions on the structure of Titan’s induced magnetosphere by conducting a systematic survey of Cassini magnetic field observations in the interaction region during flybys TA–T85 (July 2004–July 2012). We introduce a set of criteria that allow to identify deviations in the structure of Titan’s induced magnetosphere—as seen by the Cassini magnetometer (MAG)—from the picture of steady-state field line draping. These disruptions are classified as “weak”, “moderate”, or “strong”. After applying this classification scheme to all available Titan encounters, we survey the data for a possible correlation between the disruptions of the draping pattern and the ambient magnetospheric field conditions, as characterized by Simon et al. [2010a]. Our major findings are: (1) When Cassini is embedded in the northern or southern lobe of Saturn’s magnetodisk within a ` 3 h interval around closest approach, Titan’s induced magnetosphere shows little or no deviations at all from the steady-state draping picture. (2) Even when Titan is embedded in perturbed current sheet fields during an encounter, the notion of draping the average background field around the moon’s ionosphere is still applicable to explain MAG observations from numerous Titan flybys. (3) Only when Titan is exposed to intense north- south oscillations of Saturn’s current sheet at the time of an encounter, the signatures of the moon’s induced magnetosphere may be completely obscured by the ambient field perturbations. (4) So far, T70 is the only flyby that fully meets the idealized pre-Cassini picture of the Titan interaction (steady background field perpendicular to Titan’s orbital plane, steady upstream flow, unperturbed induced magnetosphere).Fil: Simon, Sven. University of Cologne. Institute of Geophysics and Meteorology; AlemaniaFil: van Treeck, Shari C.. University of Cologne. Institute of Geophysics and Meteorology; AlemaniaFil: Wennmacher, Alexandre. University of Cologne. Institute of Geophysics and Meteorology; AlemaniaFil: Saur, Joachim. University of Cologne. Institute of Geophysics and Meteorology; AlemaniaFil: Neubauer, Fritz M.. University of Cologne. Institute of Geophysics and Meteorology; AlemaniaFil: Bertucci, Cesar. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Astronomía y Física del Espacio(i); ArgentinaFil: Dougherty, Michele K.. Imperial College Of Science And Technology. Space and Atmospheric Physics Group; Reino Unid

An engineered escherichia coli strain with synthetic metabolism for in‐cell production of translationally active methionine derivatives

In the last decades, it has become clear that the canonical amino acid repertoire codified by the universal genetic code is not up to the needs of emerging biotechnologies. For this reason, extensive genetic code re‐engineering is essential to expand the scope of ribosomal protein translation, leading to reprogrammed microbial cells equipped with an alternative biochemical alphabet to be exploited as potential factories for biotechnological purposes. The prerequisite for this to happen is a continuous intracellular supply of noncanonical amino acids through synthetic metabolism from simple and cheap precursors. We have engineered an Escherichia coli bacterial system that fulfills these requirements through reconfiguration of the methionine biosynthetic pathway and the introduction of an exogenous direct trans‐sulfuration pathway. Our metabolic scheme operates in vivo, rescuing intermediates from core cell metabolism and combining them with small bio‐orthogonal compounds. Our reprogrammed E. coli strain is capable of the in‐cell production of L‐azidohomoalanine, which is directly incorporated into proteins in response to methionine codons. We thereby constructed a prototype suitable for economic, versatile, green sustainable chemistry, pushing towards enzyme chemistry and biotechnology‐based production

3D global multi-species Hall-MHD simulation of the Cassini T9 flyby

The wake region of Titan is an important component of Titan's interaction with its surrounding plasma and therefore a thorough understanding of its formation and structure is of primary interest. The Cassini spacecraft passed through the distant downstream region of Titan on 18: 59: 30 UT Dec. 26, 2005, which is referred to as the T9 flyby and provided a great opportunity to test our understanding of the highly dynamic wake region. In this paper we compare the observational data (from the magnetometer, plasma analyzer and Langmuir probe) with numerical results using a 7-species Hall MHD Titan model. There is a good agreement between the observed and modeled parameters, given the uncertainties in plasma measurements and the approximations inherent in the Hall MHD model. Our simulation results also show that Hall MHD model results fit the observations better than the non-Hall MHD model for the flyby, consistent with the importance of kinetic effects in the Titan interaction. Based on the model results, we also identify various regions near Titan where Hall MHD models are applicable

3D global multi‐species Hall‐MHD simulation of the Cassini T9 flyby

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/94961/1/grl23831.pd

Time‐dependent global MHD simulations of Cassini T32 flyby: From magnetosphere to magnetosheath

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/95383/1/jgra19655.pd

3‐D global MHD model prediction for the first close flyby of Titan by Cassini

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/95615/1/grl18965.pd

The von Hippel-Lindau Chuvash mutation in mice alters cardiac substrate and high energy phosphate metabolism

Hypoxia-inducible factor (HIF) appears to function as a global master regulator of cellular and systemic responses to hypoxia. HIF-pathway manipulation is of therapeutic interest, however global, systemic upregulation of HIF may have as yet unknown effects on multiple processes. We utilized a mouse model of Chuvash polycythemia (CP), a rare genetic disorder which modestly increases expression of HIF target genes in normoxia, to understand what these effects might be within the heart. An integrated in and ex vivo approach was employed. In comparison to wild-type controls, CP mice had evidence (using in vivo MRI) of pulmonary hypertension, right ventricular hypertrophy, and increased left ventricular ejection fraction. Glycolytic flux (measured using 3H glucose) in the isolated, contracting, perfused CP heart was 1.8-fold higher. Net lactate efflux was 1.5-fold higher. Furthermore, in vivo 13C magnetic resonance spectroscopy (MRS) of hyperpolarized 13C1 pyruvate revealed a 2-fold increase in real-time flux through lactate dehydrogenase in the CP hearts, and a 1.6-fold increase through pyruvate dehydrogenase. 31P MRS of perfused CP hearts under increased workload (isoproterenol infusion) demonstrated increased depletion of phosphocreatine relative to ATP. Intriguingly, no changes in cardiac gene expression were detected. In summary, a modest systemic dysregulation of the HIF pathway resulted in clear alterations in cardiac metabolism and energetics. However, in contrast to studies generating high HIF levels within the heart, the CP mice showed neither the predicted changes in gene expression nor any degree of LV impairment. We conclude that the effects of manipulating HIF on the heart are dose-dependent. New and noteworthy This is the first integrative metabolic and functional study of the effects of modest HIF manipulation within the heart. Of particular note, the combination (and correlation) of perfused heart metabolic flux measurements with the new technique of real-time in vivo MR spectroscopy using hyperpolarized pyruvate is a novel development

Prospective association between handgrip strength and cardiac structure and function in UK adults.

BACKGROUND: Handgrip strength, a measure of muscular fitness, is associated with cardiovascular (CV) events and CV mortality but its association with cardiac structure and function is unknown. The goal of this study was to determine if handgrip strength is associated with changes in cardiac structure and function in UK adults. METHODS AND RESULTS: Left ventricular (LV) ejection fraction (EF), end-diastolic volume (EDV), end-systolic volume (ESV), stroke volume (SV), mass (M), and mass-to-volume ratio (MVR) were measured in a sample of 4,654 participants of the UK Biobank Study 6.3 ± 1 years after baseline using cardiovascular magnetic resonance (CMR). Handgrip strength was measured at baseline and at the imaging follow-up examination. We determined the association between handgrip strength at baseline as well as its change over time and each of the cardiac outcome parameters. After adjustment, higher level of handgrip strength at baseline was associated with higher LVEDV (difference per SD increase in handgrip strength: 1.3ml, 95% CI 0.1-2.4; p = 0.034), higher LVSV (1.0ml, 0.3-1.8; p = 0.006), lower LVM (-1.0g, -1.8 --0.3; p = 0.007), and lower LVMVR (-0.013g/ml, -0.018 --0.007; p<0.001). The association between handgrip strength and LVEDV and LVSV was strongest among younger individuals, while the association with LVM and LVMVR was strongest among older individuals. CONCLUSIONS: Better handgrip strength was associated with cardiac structure and function in a pattern indicative of less cardiac hypertrophy and remodeling. These characteristics are known to be associated with a lower risk of cardiovascular events

A QTL on chromosome 3q23 influences processing speed in humans

Processing speed is a psychological construct that refers to the speed with which an individual can perform any cognitive operation. Processing speed correlates strongly with general cognitive ability, declines sharply with age, and is impaired across a number of neurological and psychiatric disorders. Thus, identifying genes that influence processing speed will likely improve understanding of the genetics of intelligence, biological aging, and the etiologies of numerous disorders. Previous genetics studies of processing speed have relied on simple phenotypes (e.g., mean reaction time) derived from single tasks. This strategy assumes, erroneously, that processing speed is a unitary construct. In the present study, we aimed to characterize the genetic architecture of processing speed by using a multi-dimensional model applied to a battery of cognitive tasks. Linkage and QTL-specific association analyses were performed on the factors from this model. The randomly ascertained sample comprised 1291 Mexican-American individuals from extended pedigrees. We found that performance on all three distinct processing-speed factors (Psychomotor Speed; Sequencing and Shifting and Verbal Fluency) were moderately and significantly heritable. We identified a genome-wide significant QTL on chromosome 3q23 for Psychomotor Speed (LOD = 4.83). Within this locus, we identified a plausible and interesting candidate gene for Psychomotor Speed (Z = 2.90, p = 1.86×10−03)

PGRMC1: a new biomarker for the estrogen receptor in breast cancer

Estrogen receptor (ER) status is a critical biomarker in breast cancer, in large part because the ER is the target of tamoxifen and similar drugs. In the previous issue of Breast Cancer Research, Neubauer and colleagues used a proteomic approach to identify proteins that are differentially regulated by ER in breast tumors. The authors showed that ER-negative tumors have elevated levels of PGRMC1 (progesterone receptor membrane component-1), a hormone receptor component and binding partner for P450 proteins. In contrast, PGRMC1 was phosphorylated in ER-positive tumors. The staining patterns of ER and PGRMC1 were mutually exclusive in breast tumor sections, and PGRMC1 staining was sharply increased in hypoxic areas of the tumor. The results suggest that PGRMC1 is a candidate biomarker for ER status and hypoxia in breast cancer