226 research outputs found

    An infrared light-guide based target positioning system for operation in a harsh environment

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    In the PANDA experiment’s hypernuclear and hyperatom setup, a positioning system for the primary production target is required, which will be located in the center of the solenoid magnet, in ultra-high vacuum, and exposed to high radiation levels. In this work, a prototype for a positioning sensor was built using a bisected light guide for infrared light and a low-priced readout system based on microcontrollers. In contrast to many modern positioning systems that require electronics in direct proximity, this setup has no active electronic components close to the moving parts. The prototype system was operated with a resolution of better than 5 μm, and with a repeatability of better than ±18 μm in a total of 14 000 measurements. The demonstrated performance is by far satisfying the positioning requirement of ±300 μm in the hypernuclear and hyperatom setup at PANDA

    The Impact of Hash Primitives and Communication Overhead for Hardware-Accelerated SPHINCS+

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    SPHINCS+ is a signature scheme included in the first NIST post-quantum standard, that bases its security on the underlying hash primitive. As most of the runtime of SPHINCS+ is caused by the evaluation of several hash- and pseudo-random functions, instantiated via the hash primitive, offloading this computation to dedicated hardware accelerators is a natural step. In this work, we evaluate different architectures for hardware acceleration of such a hash primitive with respect to its use-case and evaluate them in the context of SPHINCS+. We attach hardware accelerators for different hash primitives (SHAKE256 and Asconxof for both full and round-reduced versions) to CPU interfaces having different transfer speeds. We show, that for most use-cases, data transfer determines the overall performance if accelerators are equipped with FIFOs

    Post-Quantum Signatures on RISC-V with Hardware Acceleration

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    CRYSTALS-Dilithium and Falcon are digital signature algorithms based on cryptographic lattices, that are considered secure even if large-scale quantum computers will be able to break conventional public-key cryptography. Both schemes have been selected for standardization in the NIST post-quantum competition. In this work, we present a RISC-V HW/SW odesign that aims to combine the advantages of software- and hardware implementations, i.e. flexibility and performance. It shows the use of lexible hardware accelerators, which have been previously used for Public-Key Encryption (PKE) and Key-Encapsulation Mechanism (KEM), for post-quantum signatures. It is optimized for Dilithium as a generic signature cheme but also accelerates applications that require fast verification of Falcon’s compact signatures. We provide a comparison with previous works showing that for Dilithium and Falcon, cycle counts are significantly reduced, such that our design is faster than previous software implementations or other HW/SW codesigns. In addition to that, we present a compact Globalfoundries 22 nm ASIC design that runs at 800MHz. By using hardware acceleration, energy consumption for Dilithium is reduced by up to 92.2%, and up to 67.5% for Falcon’s signature verification

    Profiling the mouse brain endothelial transcriptome in health and disease models reveals a core blood-brain barrier dysfunction module.

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    Blood vessels in the CNS form a specialized and critical structure, the blood-brain barrier (BBB). We present a resource to understand the molecular mechanisms that regulate BBB function in health and dysfunction during disease. Using endothelial cell enrichment and RNA sequencing, we analyzed the gene expression of endothelial cells in mice, comparing brain endothelial cells with peripheral endothelial cells. We also assessed the regulation of CNS endothelial gene expression in models of stroke, multiple sclerosis, traumatic brain injury and seizure, each having profound BBB disruption. We found that although each is caused by a distinct trigger, they exhibit strikingly similar endothelial gene expression changes during BBB disruption, comprising a core BBB dysfunction module that shifts the CNS endothelial cells into a peripheral endothelial cell-like state. The identification of a common pathway for BBB dysfunction suggests that targeting therapeutic agents to limit it may be effective across multiple neurological disorders

    Capacitive crosstalk in gate-based dispersive sensing of spin qubits

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    In gate-based dispersive sensing, the response of a resonator attached to a quantum dot gate is detected by a reflected radio-frequency signal. This enables fast readout of spin qubits and tune up of arrays of quantum dots, but comes at the expense of increased susceptibility to crosstalk, as the resonator can amplify spurious signals and induce fluctuations in the quantum dot potential. We attach tank circuits with superconducting NbN inductors and internal quality factors QiQ_{\mathrm{i}}>1000 to the interdot barrier gate of silicon double quantum dot devices. Measuring the interdot transition in transport, we quantify radio-frequency crosstalk that results in a ring-up of the resonator when neighbouring plunger gates are driven with frequency components matching the resonator frequency. This effect complicates qubit operation and scales with the loaded quality factor of the resonator, the mutual capacitance between device gate electrodes, and with the inverse of the parasitic capacitance to ground. Setting qubit frequencies below the resonator frequency is expected to substantially suppress this type of crosstalk.Comment: 7 pages, 4 figures, supplementary informatio

    FuLeeca: A Lee-based Signature Scheme

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    In this work we introduce a new code-based signature scheme, called \textsf{FuLeeca}, based on the NP-hard problem of finding codewords of given Lee-weight. The scheme follows the Hash-and-Sign approach applied to quasi-cyclic codes. Similar approaches in the Hamming metric have suffered statistical attacks, which revealed the small support of the secret basis. Using the Lee metric, we are able to thwart such attacks. We use existing hardness results on the underlying problem and study adapted statistical attacks. We propose parameters for \textsf{FuLeeca}~and compare them to an extensive list of proposed post-quantum secure signature schemes including the ones already standardized by NIST. This comparison reveals that \textsf{FuLeeca}~is competitive. For example, for NIST category I, i.e., 160 bit of classical security, we obtain an average signature size of 1100 bytes and public key sizes of 1318 bytes. Comparing the total communication cost, i.e., the sum of the signature and public key size, we see that \textsf{FuLeeca} is only outperformed by Falcon while the other standardized schemes Dilithium and SPHINCS+ show larger communication costs than \textsf{FuLeeca}

    A potent antimalarial benzoxaborole targets a Plasmodium falciparum cleavage and polyadenylation specificity factor homologue.

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    Benzoxaboroles are effective against bacterial, fungal and protozoan pathogens. We report potent activity of the benzoxaborole AN3661 against Plasmodium falciparum laboratory-adapted strains (mean IC50 32 nM), Ugandan field isolates (mean ex vivo IC50 64 nM), and murine P. berghei and P. falciparum infections (day 4 ED90 0.34 and 0.57 mg kg-1, respectively). Multiple P. falciparum lines selected in vitro for resistance to AN3661 harboured point mutations in pfcpsf3, which encodes a homologue of mammalian cleavage and polyadenylation specificity factor subunit 3 (CPSF-73 or CPSF3). CRISPR-Cas9-mediated introduction of pfcpsf3 mutations into parental lines recapitulated AN3661 resistance. PfCPSF3 homology models placed these mutations in the active site, where AN3661 is predicted to bind. Transcripts for three trophozoite-expressed genes were lost in AN3661-treated trophozoites, which was not observed in parasites selected or engineered for AN3661 resistance. Our results identify the pre-mRNA processing factor PfCPSF3 as a promising antimalarial drug target

    Integration of time-series meta-omics data reveals how microbial ecosystems respond to disturbance.

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    The development of reliable, mixed-culture biotechnological processes hinges on understanding how microbial ecosystems respond to disturbances. Here we reveal extensive phenotypic plasticity and niche complementarity in oleaginous microbial populations from a biological wastewater treatment plant. We perform meta-omics analyses (metagenomics, metatranscriptomics, metaproteomics and metabolomics) on in situ samples over 14 months at weekly intervals. Based on 1,364 de novo metagenome-assembled genomes, we uncover four distinct fundamental niche types. Throughout the time-series, we observe a major, transient shift in community structure, coinciding with substrate availability changes. Functional omics data reveals extensive variation in gene expression and substrate usage amongst community members. Ex situ bioreactor experiments confirm that responses occur within five hours of a pulse disturbance, demonstrating rapid adaptation by specific populations. Our results show that community resistance and resilience are a function of phenotypic plasticity and niche complementarity, and set the foundation for future ecological engineering efforts

    Single-cell multi-omics reveals dyssynchrony of the innate and adaptive immune system in progressive COVID-19.

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    Dysregulated immune responses against the SARS-CoV-2 virus are instrumental in severe COVID-19. However, the immune signatures associated with immunopathology are poorly understood. Here we use multi-omics single-cell analysis to probe the dynamic immune responses in hospitalized patients with stable or progressive course of COVID-19, explore V(D)J repertoires, and assess the cellular effects of tocilizumab. Coordinated profiling of gene expression and cell lineage protein markers shows that S100
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