12,203 research outputs found

    Influence of skew and cross-coupling on flux-weakening performance of permanent-magnet brushless AC machines

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    A method is proposed for predicting the flux-weakening performance of permanent-magnet (PM) brushless ac machines accounting for skew and d-q axis cross-coupling. The method is based on a d-q-axis flux-linkage model, a hybrid 2-D finite-element (FE)-analytical method being used to predict the d- and q-axis inductances. However, it only requires 2-D FE analysis of the magnetic field distribution over a cross section of the machine. The developed method is used to predict the torque-speed characteristic of an interior PM brushless ac machine with one stator slot-pitch skew. This is compared with predictions from a direct FE analysis of the machine and validated by measurements

    Site-specific identification and quantitation of endogenous SUMO modifications under native conditions.

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    Small ubiquitin-like modifier (SUMO) modification regulates numerous cellular processes. Unlike ubiquitin, detection of endogenous SUMOylated proteins is limited by the lack of naturally occurring protease sites in the C-terminal tail of SUMO proteins. Proteome-wide detection of SUMOylation sites on target proteins typically requires ectopic expression of mutant SUMOs with introduced tryptic sites. Here, we report a method for proteome-wide, site-level detection of endogenous SUMOylation that uses α-lytic protease, WaLP. WaLP digestion of SUMOylated proteins generates peptides containing SUMO-remnant diglycyl-lysine (KGG) at the site of SUMO modification. Using previously developed immuno-affinity isolation of KGG-containing peptides followed by mass spectrometry, we identified 1209 unique endogenous SUMO modification sites. We also demonstrate the impact of proteasome inhibition on ubiquitin and SUMO-modified proteomes using parallel quantitation of ubiquitylated and SUMOylated peptides. This methodological advancement enables determination of endogenous SUMOylated proteins under completely native conditions

    Lifetime measurements of Triaxial Strongly Deformed bands in 163^{163}Tm

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    With the Doppler Shift Attenuation Method, quadrupole transition moments, QtQ_t, were determined for the two recently proposed Triaxial Strongly Deformed (TSD) bands in 163^{163}Tm. The measured QtQ_t moments indicate that the deformation of these bands is larger than that of the yrast, signature partners. However, the measured values are smaller than those predicted by theory. This observation appears to be valid for TSD bands in several nuclei of the regionComment: 8 pages, 5 figures. Submitted to Physical Review

    Simultaneous evolutionary expansion and constraint of genomic heterogeneity in multifocal lung cancer.

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    Recent genomic analyses have revealed substantial tumor heterogeneity across various cancers. However, it remains unclear whether and how genomic heterogeneity is constrained during tumor evolution. Here, we sequence a unique cohort of multiple synchronous lung cancers (MSLCs) to determine the relative diversity and uniformity of genetic drivers upon identical germline and environmental background. We find that each multicentric primary tumor harbors distinct oncogenic alterations, including novel mutations that are experimentally demonstrated to be functional and therapeutically targetable. However, functional studies show a strikingly constrained tumorigenic pathway underlying heterogeneous genetic variants. These results suggest that although the mutation-specific routes that cells take during oncogenesis are stochastic, genetic trajectories may be constrained by selection for functional convergence on key signaling pathways. Our findings highlight the robust evolutionary pressures that simultaneously shape the expansion and constraint of genomic diversity, a principle that holds important implications for understanding tumor evolution and optimizing therapeutic strategies.Across cancer types tumor heterogeneity has been observed, but how this relates to tumor evolution is unclear. Here, the authors sequence multiple synchronous lung cancers, highlighting the evolutionary pressures that simultaneously shape the expansion and constraint of genomic heterogeneity

    Effective electro-optical modulation with high extinction ratio by a graphene-silicon microring resonator

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    Graphene opens up for novel optoelectronic applications thanks to its high carrier mobility, ultra-large absorption bandwidth, and extremely fast material response. In particular, the opportunity to control optoelectronic properties through tuning of Fermi level enables electro-optical modulation, optical-optical switching, and other optoelectronics applications. However, achieving a high modulation depth remains a challenge because of the modest graphene-light interaction in the graphene-silicon devices, typically, utilizing only a monolayer or few layers of graphene. Here, we comprehensively study the interaction between graphene and a microring resonator, and its influence on the optical modulation depth. We demonstrate graphene-silicon microring devices showing a high modulation depth of 12.5 dB with a relatively low bias voltage of 8.8 V. On-off electro-optical switching with an extinction ratio of 3.8 dB is successfully demonstrated by applying a square-waveform with a 4 V peak-to-peak voltage.Comment: 12 pages, including 7 figure

    Deep level defects in a nitrogen-implanted ZnO homogeneous p-n junction

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    Nitrogen ions were implanted into undoped melt grown ZnO single crystals. A light-emitting p-n junction was subsequently formed by postimplantation annealing in air. Deep level transient spectroscopy was used to investigate deep level defects induced by N+ implantation and the effect of air annealing. The N+ implantation enhanced the electron trap at E C -(0.31±0.01) eV (E3) and introduced another one at E C -(0.95±0.02) eV (D1), which were removed after annealing at 900 and 750 °C, respectively. Another trap D2 (Ea =0.17±0.01 eV) was formed after the 750 °C annealing and persisted at 1200 °C. © 2008 American Institute of Physics.published_or_final_versio

    The Properties of H{\alpha} Emission-Line Galaxies at z = 2.24

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    Using deep narrow-band H2S1H_2S1 and KsK_{s}-band imaging data obtained with CFHT/WIRCam, we identify a sample of 56 Hα\alpha emission-line galaxies (ELGs) at z=2.24z=2.24 with the 5σ\sigma depths of H2S1=22.8H_2S1=22.8 and Ks=24.8K_{s}=24.8 (AB) over 383 arcmin2^{2} area in the ECDFS. A detailed analysis is carried out with existing multi-wavelength data in this field. Three of the 56 Hα\alpha ELGs are detected in Chandra 4 Ms X-ray observation and two of them are classified as AGNs. The rest-frame UV and optical morphologies revealed by HST/ACS and WFC3 deep images show that nearly half of the Hα\alpha ELGs are either merging systems or with a close companion, indicating that the merging/interacting processes play a key role in regulating star formation at cosmic epoch z=2-3; About 14% are too faint to be resolved in the rest-frame UV morphology due to high dust extinction. We estimate dust extinction from SEDs. We find that dust extinction is generally correlated with Hα\alpha luminosity and stellar mass (SM). Our results suggest that Hα\alpha ELGs are representative of star-forming galaxies (SFGs). Applying extinction correction for individual objects, we examine the intrinsic Hα\alpha luminosity function (LF) at z=2.24z=2.24, obtaining a best-fit Schechter function characterized by a faint-end slope of α=1.3\alpha=-1.3. This is shallower than the typical slope of α1.6\alpha \sim -1.6 in previous works based on constant extinction correction. We demonstrate that this difference is mainly due to the different extinction corrections. The proper extinction correction is thus key to recovering the intrinsic LF as the extinction globally increases with Hα\alpha luminosity. Moreover, we find that our Hα\alpha LF mirrors the SM function of SFGs at the same cosmic epoch. This finding indeed reflects the tight correlation between SFR and SM for the SFGs, i.e., the so-called main sequence.Comment: 15 pages, 12 figures, 2 tables, Received 2013 October 11; accepted 2014 February 13; published 2014 March 18 by Ap

    Combining NMR and LC/MS Using Backward Variable Elimination: Metabolomics Analysis of Colorectal Cancer, Polyps, and Healthy Controls

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    Both nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS) play important roles in metabolomics. The complementary features of NMR and MS make their combination very attractive; however, currently the vast majority of metabolomics studies use either NMR or MS separately, and variable selection that combines NMR and MS for biomarker identification and statistical modeling is still not well developed. In this study focused on methodology, we developed a backward variable elimination partial least-squares discriminant analysis algorithm embedded with Monte Carlo cross validation (MCCV-BVE-PLSDA), to combine NMR and targeted liquid chromatography (LC)/MS data. Using the metabolomics analysis of serum for the detection of colorectal cancer (CRC) and polyps as an example, we demonstrate that variable selection is vitally important in combining NMR and MS data. The combined approach was better than using NMR or LC/MS data alone in providing significantly improved predictive accuracy in all the pairwise comparisons among CRC, polyps, and healthy controls. Using this approach, we selected a subset of metabolites responsible for the improved separation for each pairwise comparison, and we achieved a comprehensive profile of altered metabolite levels, including those in glycolysis, the TCA cycle, amino acid metabolism, and other pathways that were related to CRC and polyps. MCCV-BVE-PLSDA is straightforward, easy to implement, and highly useful for studying the contribution of each individual variable to multivariate statistical models. On the basis of these results, we recommend using an appropriate variable selection step, such as MCCV-BVE-PLSDA, when analyzing data from multiple analytical platforms to obtain improved statistical performance and a more accurate biological interpretation, especially for biomarker discovery. Importantly, the approach described here is relatively universal and can be easily expanded for combination with other analytical technologies
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