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Daytime sky polarization calibration limitations
The daytime sky has recently been demonstrated as a useful calibration tool for deriving polarization cross-talk properties of large astronomical telescopes. The Daniel K. Inouye Solar Telescope and other large telescopes under construction can benefit from precise polarimetric calibration of large mirrors. Several atmospheric phenomena and instrumental errors potentially limit the technique’s accuracy. At the 3.67-m AEOS telescope on Haleakala, we performed a large observing campaign with the HiVIS spectropolarimeter to identify limitations and develop algorithms for extracting consistent calibrations. Effective sampling of the telescope optical configurations and filtering of data for several derived parameters provide robustness to the derived Mueller matrix calibrations. Second-order scattering models of the sky show that this method is relatively insensitive to multiple-scattering in the sky, provided calibration observations are done in regions of high polarization degree. The technique is also insensitive to assumptions about telescope-induced polarization, provided the mirror coatings are highly reflective. Zemax-derived polarization models show agreement between the functional dependence of polarization predictions and the corresponding on-sky calibrations
The fission yeast cytokinesis formin Cdc12p is a barbed end actin filament capping protein gated by profilin
Cytokinesis in most eukaryotes requires the assembly and contraction of a ring of actin filaments and myosin II. The fission yeast Schizosaccharomyces pombe requires the formin Cdc12p and profilin (Cdc3p) early in the assembly of the contractile ring. The proline-rich formin homology (FH) 1 domain binds profilin, and the FH2 domain binds actin. Expression of a construct consisting of the Cdc12 FH1 and FH2 domains complements a conditional mutant of Cdc12 at the restrictive temperature, but arrests cells at the permissive temperature. Cells overexpressing Cdc12(FH1FH2)p stop growing with excessive actin cables but no contractile rings. Like capping protein, purified Cdc12(FH1FH2)p caps the barbed end of actin filaments, preventing subunit addition and dissociation, inhibits end to end annealing of filaments, and nucleates filaments that grow exclusively from their pointed ends. The maximum yield is one filament pointed end per six formin polypeptides. Profilins that bind both actin and poly-l-proline inhibit nucleation by Cdc12(FH1FH2)p, but polymerization of monomeric actin is faster, because the filaments grow from their barbed ends at the same rate as uncapped filaments. On the other hand, Cdc12(FH1FH2)p blocks annealing even in the presence of profilin. Thus, formins are profilin-gated barbed end capping proteins with the ability to initiate actin filaments from actin monomers bound to profilin. These properties explain why contractile ring assembly requires both formin and profilin and why viability depends on the ability of profilin to bind both actin and poly-l-proline
The Solar-System-Scale Disk Around AB Aurigae
The young star AB Aurigae is surrounded by a complex combination of gas-rich
and dust dominated structures. The inner disk which has not been studied
previously at sufficient resolution and imaging dynamic range seems to contain
very little gas inside a radius of least 130 astronomical units (AU) from the
star. Using adaptive-optics coronagraphy and polarimetry we have imaged the
dust in an annulus between 43 and 302 AU from the star, a region never seen
before. An azimuthal gap in an annulus of dust at a radius of 102 AU, along
with a clearing at closer radii inside this annulus, suggests the formation of
at least one small body at an orbital distance of about 100 AU. This structure
seems consistent with crude models of mean motion resonances, or accumulation
of material at two of the Lagrange points relative to the putative object and
the star. We also report a low significance detection of a point source in this
outer annulus of dust. This source may be an overdensity in the disk due to
dust accreting onto an unseen companion. An alternate interpretation suggests
that the object's mass is between 5 and 37 times the mass of Jupiter. The
results have implications for circumstellar disk dynamics and planet formation.Comment: 11 pages, 5 figures, accepted for publication in Astrophysical
Journal, V. 680, June 10, 200
Comparative assessment of fluorescent proteins for in vivo imaging in an animal model system.
Fluorescent protein tags are fundamental tools used to visualize gene products and analyze their dynamics in vivo. Recent advances in genome editing have expedited the precise insertion of fluorescent protein tags into the genomes of diverse organisms. These advances expand the potential of in vivo imaging experiments and facilitate experimentation with new, bright, photostable fluorescent proteins. Most quantitative comparisons of the brightness and photostability of different fluorescent proteins have been made in vitro, removed from biological variables that govern their performance in cells or organisms. To address the gap, we quantitatively assessed fluorescent protein properties in vivo in an animal model system. We generated transgenic Caenorhabditis elegans strains expressing green, yellow, or red fluorescent proteins in embryos and imaged embryos expressing different fluorescent proteins under the same conditions for direct comparison. We found that mNeonGreen was not as bright in vivo as predicted based on in vitro data but is a better tag than GFP for specific kinds of experiments, and we report on optimal red fluorescent proteins. These results identify ideal fluorescent proteins for imaging in vivo in C. elegans embryos and suggest good candidate fluorescent proteins to test in other animal model systems for in vivo imaging experiments
Quantification of Proteins Using Peptide Immunoaffinity Enrichment Coupled with Mass Spectrometry
There is a great need for quantitative assays in measuring proteins. Traditional sandwich immunoassays, largely considered the gold standard in quantitation, are associated with a high cost, long lead time, and are fraught with drawbacks (e.g. heterophilic antibodies, autoantibody interference, 'hook-effect').1 An alternative technique is affinity enrichment of peptides coupled with quantitative mass spectrometry, commonly referred to as SISCAPA (Stable Isotope Standards and Capture by Anti-Peptide Antibodies).2 In this technique, affinity enrichment of peptides with stable isotope dilution and detection by selected/multiple reaction monitoring mass spectrometry (SRM/MRM-MS) provides quantitative measurement of peptides as surrogates for their respective proteins. SRM/MRM-MS is well established for accurate quantitation of small molecules 3, 4 and more recently has been adapted to measure the concentrations of proteins in plasma and cell lysates.5-7 To achieve quantitation of proteins, these larger molecules are digested to component peptides using an enzyme such as trypsin. One or more selected peptides whose sequence is unique to the target protein in that species (i.e. "proteotypic" peptides) are then enriched from the sample using anti-peptide antibodies and measured as quantitative stoichiometric surrogates for protein concentration in the sample. Hence, coupled to stable isotope dilution (SID) methods (i.e. a spiked-in stable isotope labeled peptide standard), SRM/MRM can be used to measure concentrations of proteotypic peptides as surrogates for quantification of proteins in complex biological matrices. The assays have several advantages compared to traditional immunoassays. The reagents are relatively less expensive to generate, the specificity for the analyte is excellent, the assays can be highly multiplexed, enrichment can be performed from neat plasma (no depletion required), and the technique is amenable to a wide array of proteins or modifications of interest.8-13 In this video we demonstrate the basic protocol as adapted to a magnetic bead platform
Exploring Halo Substructure with Giant Stars: The Velocity Dispersion Profiles of the Ursa Minor and Draco Dwarf Spheroidals At Large Angular Separations
We analyze velocity dispersion profiles for the Draco and Ursa Minor (UMi)
dwarf spheroidal (dSph) galaxies based on published and new Keck HIRES spectra
for stars in the outer UMi field. Washington+DDO51 filter photometric catalogs
provide additional leverage on membership of individual stars, and beyond 0.5
King limiting radii (R_lim) identify bona fide dSph members up to 4.5 times
more efficiently than simple color-magnitude diagram selections. Previously
reported ``cold populations'' R_lim are not obvious in the data and appear only
with particular binning; more or less constant and platykurtic dispersion
profiles are characteristic of these dSphs to large radii. We report discovery
of UMi stars to at least 2.7 R_lim (i.e.,210 arcmin or 4 kpc). Even with
conservative assumptions, a UMi mass of M > 4.9 x 10^8 M_(sun) is required to
bind these stars, implying an unlikely global mass-to-light ratio of M/L > 900
(M/L)_(sun). We conclude that we have found stars tidally stripped from UMi.Comment: 9 pages, 4 figures. Published in the Astrophysical Journal Letter
Drug specificity and affinity are encoded in the probability of cryptic pocket opening in myosin motor domains
The design of compounds that can discriminate between closely related target proteins remains a central challenge in drug discovery. Specific therapeutics targeting the highly conserved myosin motor family are urgently needed as mutations in at least six of its members cause numerous diseases. Allosteric modulators, like the myosin-II inhibitor blebbistatin, are a promising means to achieve specificity. However, it remains unclear why blebbistatin inhibits myosin-II motors with different potencies given that it binds at a highly conserved pocket that is always closed in blebbistatin-free experimental structures. We hypothesized that the probability of pocket opening is an important determinant of the potency of compounds like blebbistatin. To test this hypothesis, we used Markov state models (MSMs) built from over 2 ms of aggregate molecular dynamics simulations with explicit solvent. We find that blebbistatin\u27s binding pocket readily opens in simulations of blebbistatin-sensitive myosin isoforms. Comparing these conformational ensembles reveals that the probability of pocket opening correctly identifies which isoforms are most sensitive to blebbistatin inhibition and that docking against MSMs quantitatively predicts blebbistatin binding affinities (
The Lyot Project Direct Imaging Survey of Substellar Companions: Statistical Analysis and Information from Nondetections
The Lyot project used an optimized Lyot coronagraph with Extreme Adaptive
Optics at the 3.63m Advanced Electro-Optical System telescope (AEOS) to observe
86 stars from 2004 to 2007. In this paper we give an overview of the survey
results and a statistical analysis of the observed nondetections around 58 of
our targets to place constraints on the population of substellar companions to
nearby stars. The observations did not detect any companion in the substellar
regime. Since null results can be as important as detections, we analyzed each
observation to determine the characteristics of the companions that can be
ruled out. For this purpose we use a Monte Carlo approach to produce artificial
companions, and determine their detectability by comparison with the
sensitivity curve for each star. All the non-detection results are combined
using a Bayesian approach and we provide upper limits on the population of
giant exoplanets and brown dwarfs for this sample of stars. Our nondetections
confirm the rarity of brown dwarfs around solar-like stars and we constrain the
frequency of massive substellar companions (M>40Mjup) at orbital separation
between and 10 and 50 AU to be <20%.Comment: 32 pages, 11 figures, 2 tables. Published in the Astrophysical
Journa
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