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Employing a cleavable carbohydrate–peptide linker, a new strategy for single-bead analysis of multivalent cyclic neoglycopeptides based on Edman degradation is described. Edman degradation of glycopeptides is hampered by the acid lability of the glycosidic bond and potential incompatibilities of phenylthiohydantoin (PTH) derivatives of glycosylated amino acids with PTH derivatives of the proteinogenic amino acids. To overcome this problem, carbohydrates are detached from the cyclopeptide templates before single-bead analysis, allowing for micro sequencing under routine conditions. With this strategy, application of multivalent cyclic neoglycopeptides in split-mix libraries with a subsequent screening process becomes possible for the first time. 相似文献
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In spherically symmetric systems, in spite of Birkhoff's Theorem, the rates of clocks in vacuum regions on either side of moving mass shells must be continually readjusted to stay in synchrony. This shows up as time-dependence of the metric in terms of the globally meaningful time coordinate. 相似文献
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Roland A. Fischer Heinz-Josef Kneuper Wolfgang A. Hermann 《Journal of organometallic chemistry》1987,330(3):365-376
Hydrogenchalcogenido complexes of general composition (η5-C5R5)(CO)3M(EH) (R = H, CH3; M = Cr, Mo, W; E = S, Se) can be obtained by three different routes, sometimes in quite good yields. Thus, the sulfur and selenium derivatives can be synthesized by insertion of the respective elements into the metal-hydrogen bonds of the precursor compounds (η5-C5R5)(CO)3MH. This species also reacts with potassium selenocyanate to yield the hydrogenselenido derivatives (η5-C5R5)(CO)3M(SeH) which can also be obtained by treatment of the methyl complexes (η5-C5R5)(CO)3M(CH3 (M = Mo, W) with HBF4 and Li[SeH]. The corresponding hydrogentellurido compounds are probably formed by these preparative methods but appear to be quickly converted into either the dinuclear tellurium bridge products (μ-Te)[(η5-C5R5)(CO)3M]2 (M = Mo) or into the hydrido complexes (η5-C5R5)(CO)3MH (M= Mo, W) by release of elemental tellurium. 相似文献
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In an exterior domain Ω??n, n ? 2, we consider the generalized Stokes resolvent problem in Lq-space where the divergence g = div u and inhomogeneous boundary values u = ψ with zero flux ∫?Ωψ·N do = 0 may be prescribed. A crucial step in our approach is to find and to analyse the right space for the divergence g. We prove existence, uniqueness and a priori estimates of the solution and get new results for the divergence problem. Further, we consider the non-stationary Stokes system with non-homogeneous divergence and boundary values and prove estimates of the solution in L5(0, T;Lq(Ω)) for 1 < s, q < ∞. 相似文献
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Hermann Grabert Gert-Ludwig Ingold Michel H. Devoret Daniel Estève Hugues Pothier Cristian Urbina 《Zeitschrift für Physik B Condensed Matter》1991,84(1):143-155
The rate of electron tunneling through normal metal tunnel junctions is calculated for the case of ultrasmall junction capacitances. The so-called Coulomb blockade of electron tunneling at low temperatures is shown to be strongly affected by the external electrical circuit. Under the common experimental condition of a low impedance environment the Coulomb blockade is suppressed for single tunnel junctions. However, a Coulomb gap structure emerges for junctions embedded in a high impedance environment. For a double junction setup a Coulomb blockade of tunneling arises even for low impedance environments due to the charge quantization on the metallic island between the junctions. An approach using circuit analysis is presented which allows to reduce the calculation of tunneling rates in multijunction circuits to those of a single junction in series with an effective capacitance. The range of validity of the socalled local rule and global rule rates is clarified. It is found that the tunneling rate tends towards the global rule rate as the number of junctions is increased. Some specific results are given for a one-dimensional array of tunnel junctions. 相似文献
8.
Michaela Capellmann Hermann M. Bolt 《Fresenius' Journal of Analytical Chemistry》1992,342(4-5):462-466
Summary A reproducible method is described for the separation and simultaneous and specific quantitation of ascorbic acid and dehydroascorbic acid by ion-pairing reversed-phase HPLC with fluorometric detection. Copper sulphate and copper acetate were compared as oxidizing reagents for ascorbic acid and 1,2-diaminobenzene dihydrochloride and 1,2-diamino-3,4-dimethylbenzene dihydrochloride as derivatising reagents. The HPLC-method was applied to human plasma. The detection limit reaches 16 ng for ascorbic acid and 3 ng for dehydroascorbic acid. Sample preparation is carried out by solid phase extraction with a recovery of 98%; it is compared with conventional precipitation of plasma proteins by metaphosphoric acid. 相似文献
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