128 research outputs found
Cold inelastic collisions between lithium and cesium in a two-species magneto-optical trap
We investigate collisional properties of lithium and cesium which are
simultaneously confined in a combined magneto-optical trap. Trap-loss
collisions between the two species are comprehensively studied. Different
inelastic collision channels are identified, and inter-species rate
coefficients as well as cross sections are determined. It is found that loss
rates are independent of the optical excitation of Li, as a consequence of the
repulsive Li-Cs interaction. Li and Cs loss by inelastic inter-species
collisions can completely be attributed to processes involving optically
excited cesium (fine-structure changing collisions and radiative escape). By
lowering the trap depth for Li, an additional loss channel of Li is observed
which results from ground-state Li-Cs collisions changing the hyperfine state
of cesium.Comment: submitted to Euro. Phys. J. D, special issue on Laser Cooling and
Trappin
Nuclear Resonance Vibrational Spectroscopy of Iron Sulfur Proteins
Nuclear inelastic scattering in conjunction with density functional theory
(DFT) calculations has been applied for the identification of vibrational modes
of the high-spin ferric and the high-spin ferrous iron-sulfur center of a
rubredoxin-type protein from the thermophylic bacterium Pyrococcus abysii
Autler-Townes splitting in two-color photoassociation of 6Li
We report on high-resolution two-color photoassociation spectroscopy in the
triplet system of magneto-optically trapped 6Li. The absolute transition
frequencies have been measured. Strong optical coupling of the bound molecular
states has been observed as Autler-Townes splitting in the photoassociation
signal. The spontaneous bound-bound transition rate is determined and the
molecule formation rate is estimated. The observed lineshapes are in good
agreement with the theoretical model.Comment: 5 pages, 4 figures, accepted for publication in Phys. Rev. A (Rapid
Communication
Improving the use of research evidence in guideline development: 1. Guidelines for guidelines
BACKGROUND: The World Health Organization (WHO), like many other organisations around the world, has recognised the need to use more rigorous processes to ensure that health care recommendations are informed by the best available research evidence. This is the first of a series of 16 reviews that have been prepared as background for advice from the WHO Advisory Committee on Health Research to WHO on how to achieve this. OBJECTIVES: We reviewed the literature on guidelines for the development of guidelines. METHODS: We searched PubMed and three databases of methodological studies for existing systematic reviews and relevant methodological research. We did not conduct systematic reviews ourselves. Our conclusions are based on the available evidence, consideration of what WHO and other organisations are doing and logical arguments. KEY QUESTIONS AND ANSWERS: We found no experimental research that compared different formats of guidelines for guidelines or studies that compared different components of guidelines for guidelines. However, there are many examples, surveys and other observational studies that compared the impact of different guideline development documents on guideline quality. WHAT HAVE OTHER ORGANIZATIONS DONE TO DEVELOP GUIDELINES FOR GUIDELINES FROM WHICH WHO CAN LEARN? • Establish a credible, independent committee that evaluates existing methods for developing guidelines or that updates existing ones. • Obtain feedback and approval from various stakeholders during the development process of guidelines for guidelines. • Develop a detailed source document (manual) that guideline developers can use as reference material. WHAT SHOULD BE THE KEY COMPONENTS OF WHO GUIDELINES FOR GUIDELINES? • Guidelines for guidelines should include information and instructions about the following components: 1) Priority setting; 2) Group composition and consultations; 3) Declaration and avoidance of conflicts of interest; 4) Group processes; 5) Identification of important outcomes; 6) Explicit definition of the questions and eligibility criteria ; 7) Type of study designs for different questions; 8) Identification of evidence; 9) Synthesis and presentation of evidence; 10) Specification and integration of values; 11) Making judgments about desirable and undesirable effects; 12) Taking account of equity; 13) Grading evidence and recommendations; 14) Taking account of costs; 15) Adaptation, applicability, transferability of guidelines; 16) Structure of reports; 17) Methods of peer review; 18) Planned methods of dissemination & implementation; 19) Evaluation of the guidelines. WHAT HAVE OTHER ORGANIZATIONS DONE TO IMPLEMENT GUIDELINES FOR GUIDELINES FROM WHICH WHO CAN LEARN? • Obtain buy-in from regions and country level representatives for guidelines for guidelines before dissemination of a revised version. • Disseminate the guidelines for guidelines widely and make them available (e.g. on the Internet). • Develop examples of guidelines that guideline developers can use as models when applying the guidelines for guidelines. • Ensure training sessions for those responsible for developing guidelines. • Continue to monitor the methodological literature on guideline development
Elucidating the structural composition of a Fe-N-C catalyst by nuclear and electron resonance techniques
Fe–N–C catalysts are very promising materials for fuel cells and metal–air batteries. This work gives fundamental insights into the structural composition of an Fe–N–C catalyst and highlights the importance of an in‐depth characterization. By nuclear‐ and electron‐resonance techniques, we are able to show that even after mild pyrolysis and acid leaching, the catalyst contains considerable fractions of α‐iron and, surprisingly, iron oxide. Our work makes it questionable to what extent FeN4 sites can be present in Fe–N–C catalysts prepared by pyrolysis at 900 °C and above. The simulation of the iron partial density of phonon states enables the identification of three FeN4 species in our catalyst, one of them comprising a sixfold coordination with end‐on bonded oxygen as one of the axial ligands
Improving the use of research evidence in guideline development: 9. Grading evidence and recommendations
BACKGROUND: The World Health Organization (WHO), like many other organisations around the world, has recognised the need to use more rigorous processes to ensure that health care recommendations are informed by the best available research evidence. This is the ninth of a series of 16 reviews that have been prepared as background for advice from the WHO Advisory Committee on Health Research to WHO on how to achieve this. OBJECTIVES: We reviewed the literature on grading evidence and recommendations in guidelines. METHODS: We searched PubMed and three databases of methodological studies for existing systematic reviews and relevant methodological research. We did not conduct a full systematic review ourselves. Our conclusions are based on the available evidence, consideration of what WHO and other organisations are doing and logical arguments. KEY QUESTIONS AND ANSWERS: Should WHO grade the quality of evidence and the strength of recommendations? • Users of recommendations need to know how much confidence they can place in the underlying evidence and the recommendations. The degree of confidence depends on a number of factors and requires complex judgments. These judgments should be made explicitly in WHO recommendations. A systematic and explicit approach to making judgments about the quality of evidence and the strength of recommendations can help to prevent errors, facilitate critical appraisal of these judgments, and can help to improve communication of this information. What criteria should be used to grade evidence and recommendations? • Both the quality of evidence and the strength of recommendations should be graded. The criteria used to grade the strength of recommendations should include the quality of the underlying evidence, but should not be limited to that. • The approach to grading should be one that has wide international support and is suitable for a wide range of different types of recommendations. The Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach, which is currently suggested in the Guidelines for WHO Guidelines, is being used by an increasing number of other organizations internationally. It should be used more consistently by WHO. Further developments of this approach should ensure its wide applicability. Should WHO use the same grading system for all of its recommendations? • Although there are arguments for and against using the same grading system across a wide range of different types of recommendations, WHO should use a uniform grading system to prevent confusion for developers and users of recommendations
Saturation in heteronuclear photoassociation of 6Li7Li
We report heteronuclear photoassociation spectroscopy in a mixture of
magneto-optically trapped 6Li and 7Li. Hyperfine resolved spectra of the
vibrational level v=83 of the singlet state have been taken up to intensities
of 1000 W/cm^2. Saturation of the photoassociation rate has been observed for
two hyperfine transitions, which can be shown to be due to saturation of the
rate coefficient near the unitarity limit. Saturation intensities on the order
of 40 W/cm^2 can be determined.Comment: 5 pages, 3 figures, to appear in Phys. Rev. A (Rapid Communication
Two-species mixture of quantum degenerate Bose and Fermi gases
We have produced a macroscopic quantum system in which a Li-6 Fermi sea
coexists with a large and stable Na-23 Bose-Einstein condensate. This was
accomplished using inter-species sympathetic cooling of fermionic Li-6 in a
thermal bath of bosonic Na-23
Ultra-cold atoms in an optical cavity: two-mode laser locking to the cavity avoiding radiation pressure
The combination of ultra-cold atomic clouds with the light fields of optical
cavities provides a powerful model system for the development of new types of
laser cooling and for studying cooperative phenomena. These experiments
critically depend on the precise tuning of an incident pump laser with respect
to a cavity resonance. Here, we present a simple and reliable experimental
tuning scheme based on a two-mode laser spectrometer. The scheme uses a first
laser for probing higher-order transversal modes of the cavity having an
intensity minimum near the cavity's optical axis, where the atoms are confined
by a magnetic trap. In this way the cavity resonance is observed without
exposing the atoms to unwanted radiation pressure. A second laser, which is
phase-locked to the first one and tuned close to a fundamental cavity mode
drives the coherent atom-field dynamics.Comment: 7 pages, 7 figure
Neutralization of SARS-CoV-2 by highly potent, hyperthermostable, and mutation-tolerant nanobodies
Monoclonal anti-SARS-CoV-2 immunoglobulins represent a treatment option for COVID-19. However, their production in mammalian cells is not scalable to meet the global demand. Single-domain (VHH) antibodies (also called nanobodies) provide an alternative suitable for microbial production. Using alpaca immune libraries against the receptor-binding domain (RBD) of the SARS-CoV-2 Spike protein, we isolated 45 infection-blocking VHH antibodies. These include nanobodies that can withstand 95°C. The most effective VHH antibody neutralizes SARS-CoV-2 at 17–50 pM concentration (0.2–0.7 µg per liter), binds the open and closed states of the Spike, and shows a tight RBD interaction in the X-ray and cryo-EM structures. The best VHH trimers neutralize even at 40 ng per liter. We constructed nanobody tandems and identified nanobody monomers that tolerate the K417N/T, E484K, N501Y, and L452R immune-escape mutations found in the Alpha, Beta, Gamma, Epsilon, Iota, and Delta/Kappa lineages. We also demonstrate neutralization of the Beta strain at low-picomolar VHH concentrations. We further discovered VHH antibodies that enforce native folding of the RBD in the E. coli cytosol, where its folding normally fails. Such “fold-promoting” nanobodies may allow for simplified production of vaccines and their adaptation to viral escape-mutations
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