| 1. |
- Donoghue, Philip C. J., et al.
(författare)
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Synchrotron X-ray tomographic microscopy of fossil embryos
- 2006
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Ingår i: Nature. - 0028-0836. ; 442:7103, s. 601-718
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Tidskriftsartikel (refereegranskat)abstract
- Fossilized embryos from the late Neoproterozoic and earliest Phanerozoic have caused much excitement because they preserve the earliest stages of embryology of animals that represent the initial diversification of metazoans1, 2, 3, 4. However, the potential of this material has not been fully realized because of reliance on traditional, non-destructive methods that allow analysis of exposed surfaces only1, 2,3, 4, and destructive methods that preserve only a single two-dimensional view of the interior of the specimen5, 6. Here, we have applied synchrotron-radiation X-ray tomographic microscopy (SRXTM)7, obtaining complete three-dimensional recordings at submicrometre resolution. The embryos are preserved by early diagenetic impregnation and encrustation with calcium phosphate, and differences in X-ray attenuation provide information about the distribution of these two diagenetic phases. Three-dimensional visualization of blastomere arrangement and diagenetic cement in cleavage embryos resolves outstanding questions about their nature, including the identity of the columnar blastomeres. The anterior and posterior anatomy of embryos of the bilaterian worm-like Markuelia confirms its position as a scalidophoran, providing new insights into body-plan assembly among constituent phyla. The structure of the developing germ band in another bilaterian, Pseudooides, indicates a unique mode of germ-band development. SRXTM provides a method of non-invasive analysis that rivals the resolution achieved even by destructive methods, probing the very limits of fossilization and providing insight into embryology during the emergence of metazoan phyla.
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| 2. |
- Shi, F., et al.
(författare)
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Synthesis and characterization of two novel high valent dinuclear complexes with a triphenolate ligand bearing functional groups
- 2005
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Ingår i: Chinese Chemical Letters. - 1001-8417 .- 1878-5964. ; 16:1, s. 89-92
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Tidskriftsartikel (refereegranskat)abstract
- Two novel high valent complexes [M-2(III, III)L(mu-OAc)(2)](PF6)-P-. (M=Mn, Fe; 9) were prepared, where L was the tri-anion of 2,6-bis{[(2-hydroxy-3-(morpholin-4-yl methyl)-5-tertbutyl benzyl)(pyridyl-2-methyl)amino]methyl}-4-methyl phenol which contained additional phenolic, tert-butyl and morpholin-4-yl methyl groups compared to its parent [Mn-2(II, II)(bpmp) (mu-OAc)(2)](CIO4)-C-. (10). These improvements decreased the difference between the new model and (Mn)(4) cluster (OEC in nature).
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| 3. |
- Sun, Shiguo, et al.
(författare)
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Intra- and intermolecular interaction ECL study of novel ruthenium tris-bipyridyl complexes with different amine reductants
- 2009
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Ingår i: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; :38, s. 7969-7974
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Tidskriftsartikel (refereegranskat)abstract
- A series of ruthenium(II) tris-bipyridyl complexes covalently linked with different amine reductants such as tripropylamine (TPrA), ethanolamine and diethanolamine for an electrochemiluminescence (ECL) system have been synthesized. Their ECL property at different working electrodes has been studied with and without the presence of TPrA, triethanolamine (TEOA) and 2-(dibutylamino) ethanol (DBAE) as the coreactant, respectively. The results demonstrate that the conjugated ruthenium complex alone can generate ECL through intramolecular interaction at a relatively low concentration, while with intermolecular interaction the ECL intensity increases progressively and becomes increasingly dominant with increasing complex concentration. For the coreactant system ECL, the amine coreactant needed for the conjugate complexes can be significantly lowered in comparison with that of the well known [Ru(bpy)(3)](2+)/TPrA system. One amine substituent is better for the system in order to diminish the steric hindrance, and the intramolecular amine reductant employed should have a similar structure with that of the additive amine coreactant to achieve a good ECL performance, which can pave a new route to further improving the ECL efficiency and increase the sensitivity of detection through combining both intra-and intermolecular interaction.
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| 4. |
- Sun, Shiguo, et al.
(författare)
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Study of Highly Efficient Bimetallic Ruthenium Tris-bipyridyl ECL Labels for Coreactant System
- 2009
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Ingår i: Analytical Chemistry. - : American Chemical Society (ACS). - 0003-2700 .- 1520-6882. ; 81:24, s. 10227-10231
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Tidskriftsartikel (refereegranskat)abstract
- A series of bimetallic ruthenium complexes [(bpy)(2)Ru(bpy)(CH2)(n)(bpy)Ru(bpy)(2)](4+) (1, where bpy is 2,2'-bipyridinyl, n = 3, 5, 8) for the coreactant electrochemiluminescence (ECL) system have been synthesized. Their ECL property at different working electrode has been studied in 0.1 M phosphate buffer by using tripropylamine (TPrA) and 2-(dibutylamino) ethanol (DBAE) as the coreactant. The results demonstrate that the ECL intensity depends largely on the length of the saturated carbon chain linkage: the longer is the carbon chain, the higher is the ECL intensity. A remarkable ECL enhancement (up to about 25 times), in comparison with the commonly used metallic [Ru(bpy)(3)](2+), has been observed from 1c (n = 8) at Pt electrode. With 20 mM TPrA, the log of the ECL intensity increases linearly with the log of complex 1c concentrations over the concentration range of 1.0 x 10(-16) to 1.0 x 10(-6) M at glassy carbon electrode. The detection limit is 1.0 x 10(-16) M at a signal-to-noise ratio of 3. This is the highest ECL detection limit for bimetallic system reported until now. The study provides a general methodology to further improve and tune the ECL efficiency by using multimetallic ruthenium complexes.
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| 5. |
- Wu, Peng, et al.
(författare)
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A novel methodology for synthesizing crystalline metallosilicates with expanded pore windows through molecular alkoxysilylation of zeolitic lamellar precursor
- 2008
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Ingår i: Journal of the American Chemical Society. - : American Chemical Society. - 0002-7863 .- 1520-5126. ; 130:26, s. 8178-8187
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Tidskriftsartikel (refereegranskat)abstract
- Postalkoxysilylation with diethoxydimethylsilane has been carried out on the zeolitic lamellar precursors of various topologies such as MWW, FER, CDO and MCM-47 aiming to construct new crystalline structures with expanded pore apertures between the layers. The silylation process and the crystalline and pore structures of the resulting materials have been investigated with the techniques of XRD, IR, 13C and 29Si MAS NMR, ICP, SEM, HRTEM, elemental analyses, and N2 adsorption. In contrast to forming known three-dimensional zeolite structures after direct calcination of the lamellar precursors, the silylation led to new crystalline structures with opener pores, as evidenced by the shift of layer-related diffractions to the lower-angle region in XRD patterns and the enlarged interlayer pores found by HRTEM images. After optimizing the treatment conditions, particularly the amount of silane agent, a maximum and homogeneous silylation was realized, which guaranteed the phase purity in interlayer expanded zeolites. The expanded structures were well preserved after calcination at 823 K or reflux in water for 1 to 2 weeks, indicating a high thermal stability and also a hydrothermal stability. The interlayer expanded zeolites prepared from the metallosilicate precursors of MWW topology exhibited higher catalytic activities in the redox and solid acid-catalyzed reactions of bulky molecules than that of their counterparts with conventional MWW topology.
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| 6. |
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| 7. |
- Zhang, Tongyan, et al.
(författare)
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Redox-induced partner radical formation and its dynamic balance with radical dimer in cucurbit 8 uril
- 2009
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Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 11:47, s. 11134-11139
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Tidskriftsartikel (refereegranskat)abstract
- N-(4-Hydroxy-phenoxyethyl)-N'-ethyl-4,4'-bipyridium (1) can form a stable 1 : 1 inclusion complex with CB[8] in aqueous solution, in which the hydroxyphenol (HP) moiety is back-folded and inserted together with the viologen moiety into the cavity of CB[8]. When the ethyl viologen dication (EV2+) in 1 is reduced, chemically or electrochemically, an intramolecular partner radical (EV+center dot-HP)/CB[8] can be detected, meanwhile, a dynamic balance between the partner radical and the intermolecular radical dimer (EV+center dot-HP)(2)/CB[8] can be observed.
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| 8. |
- Zhao, Peng, et al.
(författare)
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Lentiviral vector mediated siRNA knock-down of hTERT results in diminished capacity in invasiveness and in vivo growth of human glioma cells in a telomere length-independent manner
- 2007
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Ingår i: International Journal of Oncology. - 1019-6439. ; 31:2, s. 361-368
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Tidskriftsartikel (refereegranskat)abstract
- Glioma cells are characterized by their invasiveness and resistance against conventional therapeutics. Telomerase activity has been suggested to be an important target for glioma treatment. Here we assessed the anticancer effects and its potential mechanisms of lentiviral vector mediated siRNA knock-down of the human telomerase reverse transcriptase (hTERT) in U87MG human glioblastoma cells. Stable expression of anti-hTERT siRNA reduced the hTERT expression and TRAP assay telomerase activity to barely detectable levels. Injection of lentiviral vectors encoding anti-hTERT siRNA significantly inhibited the growth of preestablished macroscopic xenograft tumors, which was in contrast to the finding that no obvious effects on cell growth, cell cycle progression and telomere length were observed in anti-hTERT siRNA expressing U87MG cells during short-term in vitro cultures. The in vivo glioma growth inhibition effect was already evident in the period coincided with no detectable telomere length changes, suggesting that hTERT inhibition may hinder glioma cell growth in a telomere length-independent manner. Importantly, transwell migration assay showed profound inhibitory effect on the invasive capacity of U87MG cells following short-term anti-hTERT siRNA expression. Thus, efficient knock-down of hTERT can inhibit glioma cell proliferation and migration prior to its effect on telomere length.
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