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J. Zhuang W. Kunnmann L.M. Corliss J.M. Hastings R.O. Moyer 《Journal of solid state chemistry》1983,48(1):117-120
A powder neutron diffraction study of Eu1532IrD5 has shown it to be isostructural with Sr2IrD5 at room temperature. Unlike the latter compound, it does not undergo a deuterium-ordering transition at low temperatures. Magnetic scattering at helium temperatures confirms the suggestion that it becomes ferromagnetic below 20 K with a moment corresponding to that of divalent europium. 相似文献
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R. Hastings A. Pollak P. P. Saitschenko W. P. Rshechin N. O. Pogonkina L. Krupitzkaja K. Kochowa Ph. Mc G. Shuey M. Rosumny A. de Rosset D. B. Johns und W. W. Ssemenowa 《Fresenius' Journal of Analytical Chemistry》1940,119(7-8):305-307
Ohne Zusammenfassung 相似文献
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J. W. Hastings Shiao-Chun Tu James E. Becvar ‡ Robert P. Presswood 《Photochemistry and photobiology》1979,29(2):383-387
Abstract— The bioluminescent oxidation of reduced flavin mononucleotide by bacterial luciferase involves a long-lived flavoenzyme intermediate whose chromophore has been postulated to be the 4a-sub-stituted peroxy anion of reduced flavin. Reaction of long chain aldehyde with this intermediate results in light emission and formation of the corresponding acid. These experiments show that the typical aldehyde-dependent, luciferase-catalyzed bioluminescence can also be obtained starting with FMN and H2 O2 instead of FMNH2 and O2 . We postulate that the 4a-peroxy anion intermediate is formed directly by attack of H2 O2 on FMN. The latter may be bound to luciferase. An enzyme bound intermediate is formed which by kinetic analysis, flavin specificity for luminescence, aldehyde dependence, and bioluminescent emission spectrum appears to be identical with the species generated by reaction of FMNH, and O2 with luciferase. The quantum yield of the H2 O2 -- and FMN-initiated biolumlnescence is low but can be enhanced by certain metal ions, which also stimulate a chemiluminescent reaction of oxidized flavin with H2 O2 . The peak of this chemiluminescence. however, appears to be at a shorter wavelength than that (490 nm) of the bioluminescence. 相似文献
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Chen ZW Chen LH Akentieva N Lichti CF Darbandi R Hastings R Covey DF Reichert DE Townsend RR Evers AS 《Electrophoresis》2012,33(4):666-674
Previous studies have shown that the neurosteroid analogue, 6-Azi-pregnanolone (6-AziP), photolabels voltage-dependent anion channels and proteins of approximately 55 kDa in rat brain membranes. The present study used two-dimensional electrophoresis and nanoelectrospray ionization ion-trap mass spectrometry (nano-ESI-MS) to identify the 55 kDa proteins (isoelectric point 4.8) as isoforms of β-tubulin. This identification was confirmed by immunoblot and immunoprecipitation of photolabeled protein with anti-β-tubulin antibody and by the demonstration that 6-AziP photolabels purified bovine brain tubulin in a concentration-dependent pattern. To identify the photolabeling sites, purified bovine brain tubulin was photolabeled with 6-AziP, digested with trypsin, and analyzed by matrix-assisted laser desorption/ionization MS (MALDI). A 6-AziP adduct of TAVCDIPPR(m/z?= 1287.77), a β-tubulin specific peptide, was detected by MALDI. High-resolution liquid chromatography-MS/MS analysis identified that 6-AziP was covalently bound to cysteine 354 (Cys-354), previously identified as a colchicine-binding site. 6-AziP photolabeling was inhibited by 2-methoxyestradiol, an endogenous derivative of estradiol thought to bind to the colchicine site. Structural modeling predicted that neurosteroids could dock in this colchicine site at the interface between α- and β-tubulin with the photolabeling group of 6-AziP positioned proximate to Cys-354. 相似文献
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Jian Zhuang Julius M. Hastings Lester M. Corliss R. Bau Chiau-Yu Wei R. O. Moyer Jr. 《Journal of solid state chemistry》1981,40(3):352-360
Neutron diffraction data have been collected on a powdered sample of Sr2IrD5 over a range of temperatures. The compound, which is cubic at room temperature, has been found to exhibit a gradual transformation to a tetragonal phase in the temperature range 200-140 K. As a result of the transition, deuterium atoms which randomly occupy sixfold positions in the cubic phase, become tetragonally ordered. A small fraction of the cubic phase remained untransformed at 4.2 K. Both the cubic and tetragonal structures are consistent with square pyramidal IrD5 units with average Ir---D distances of 1.714 and 1.718 Å, respectively. Agreement factors, R1, for the two structural analyses are 3.44 and 4.94%. 相似文献