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31.
Akito Tsuboi 《Mathematical Logic Quarterly》1992,38(1):101-106
In this note we treat maximal and minimal normal subgroups of a superstable group and prove that these groups are definable under certain conditions. Main tool is a superstable version of Zil'ber's indecomposability theorem. MSC: 03C60. 相似文献
32.
Kashiwada A Tsuboi M Matsuda K 《Langmuir : the ACS journal of surfaces and colloids》2011,27(4):1403-1408
The coiled coil trimer structure is a common motif observed in membrane fusion processes of specific fusion proteins such as the hemagglutinin glycoprotein. The HA2 subunit in the hemagglutinin changes its conformation or geometry to be favorable to membrane fusion in response to endosomal weakly acidic pH. This pH responsiveness is indispensable to an artificial polypeptide-triggered delivery system as well as the membrane fusion reaction in biology. In this study, we have constructed an AAB-type coiled coil heteroassembled system that is sensitive to weakly acidic pH. The heterotrimer is formed from two kinds of polypeptides containing an Ala or a Trp residue at a hydrophobic a position, and it was observed that the Glu residue at the other a position induced an acidic pH-dependent conformational change. On the basis of this pH-responsive coiled coil heteroassembled system, a boronic acid coupled working polypeptide for the combination of an intervesicular complex with a sugarlike compound on the surface of the target liposome, and a supporting polypeptide for the construction of a pH-responsive heterotrimer with the working polypeptide were designed and synthesized. The process of membrane fusion was characterized by lipid-mixing, inner-leaflet lipid-mixing, and content-mixing assays. The target selective vesicle fusion is clearly observed at a weakly acidic pH, where the working polypeptides form a heterotrimeric coiled coil with the supporting polypeptides in a 1:2 binding stoichiometry and the surfaces between pilot and target vesicles come into close proximity to each other. 相似文献
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34.
Eu(2+)-doped monophosphates NaSrPO(4) and KBaPO(4) with the β-K(2)SO(4) structure were synthesized using the conventional high temperature solid state reaction. The X-ray powder diffraction, photoluminescence excitation, and emission spectra and decay curves were measured. The phosphors can be efficiently excited by UV-visible light from 220 to 430 nm to realize emission in the visible range. The natures of the Eu(2+) emission, e.g., the chromaticity coordinates, the Stokes shifts, and the luminescence absolute quantum efficiencies, were reported. The luminescence quenching temperatures and the thermal activation energies for NaSrPO(4):Eu(2+) and KBaPO(4):Eu(2+) were obtained from the temperature dependent (10-435 K) luminescence intensities and decay curves. KBaPO(4):Eu(2+) presents only one emission center; however, Eu(2+) ions have a "disordered environment" in NaSrPO(4) lattices. The relationship between the luminescence thermal stabilities and the crystal structures was discussed. The crystallographic occupations of rare earth ions doped in these hosts were analyzed by the site-selective emission spectra and the excitation spectra of Eu(3+) ions in the (7)F(0)→(5)D(0) transitions using a pulsed, tunable, and narrow-band dye laser. In KBaPO(4), the Eu(3+) ions could be distributed in the host with a high "ordered state" in only one site in the lattices. However, the multiple site structure of Eu(3+) ions with highly disordered distributions in NaSrPO(4) lattices was suggested. 相似文献
35.
Yasuyuki Tsuboi Kensaku Okada Shoji Ishizaka Noboru Kitamura 《Analytical sciences》2005,21(3):303-308
We found that alpha-diketones (2,3-butanedione (BD) and 1-phenyl-1,2-propanedione (PPD)) were very suitable luminescence probes for studying the properties of a perfluorinated solvent (i.e., fluorous solvent; perfluoromethylcyclohexane (PFMC)), since these compounds were soluble in PFMC and showed long-lived phosphorescence even at room temperature. The phosphorescence lifetime (tau(p)) of BD in PFMC (650 micros) was much longer than that in cyclohexane (CH, 270 micros). The longer tau(p) value of BD in PFMC was ascribed to the variation of the intersystem crossing rate constant (k(isc)) from the excited triplet state (T1) to the ground state (S0) with the solvent. Some possible reasons for the change in k(isc) were discussed in terms of solute-solvent interactions. Furthermore, by utilizing phosphorescence quenching of BD by pyrene, we, determined a rate constant of the diffusion-controlled reaction in PFMC. Characteristic behaviors of mixing/separation processes between PFMC and a common organic solvent observed by Schlieren photographs were also reported. 相似文献
36.
Yoshiaki Hamada Kazuko Hashiguchi Masamichi Tsuboi Yoshinori Koga Shigeo Kondo 《Journal of Molecular Spectroscopy》1984,105(1):70-80
Methyleneimine was detected in the gas phase by a moderately high resolution infrared spectrometer as one of the intermediate species produced by a pyrolysis of amines. Observed vibrational frequencies of some isotopic derivatives have been combined with the ab initio values to reach a most reliable force constants set. Some other spectroscopic parameters, involving geometrical parameters and dipole moment derivatives, have also been calculated ab initio and compared with the observation. Its half-life in our experimental apparatus was about 10 min, which is much longer than the previously reported values, 0.1 or 10 sec. 相似文献
37.
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39.
Yoshiaki Amatatsu Yoshiaki Hamada Masamichi Tsuboi Masaaki Sugie 《Journal of Molecular Spectroscopy》1985,111(1):29-41
The infrared spectrum of N-methylvinylamine was observed for the first time in the gas phase by the pyrolysis of propyleneimine. The half-life of this molecule was about 40 sec under our experimental conditions, and the molecule isomerized immediately into its tautomer, N-methylethylideneimine. The absorption bands were assigned by the help of an ab initio MO calculation. 相似文献
40.
An ab initio Mo method was applied to analyse the vibrational spectra of amines and their pyrolytic products. The result was useful to predict the frequencies of group vibrations, and to explain the characteristics of molecular parameters. The relative populations of rotational conformers were calculated and the results were found to be in qualitative agreement with what were observed. 相似文献