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31.
本文在SAND迭代法的基础上,采取带有周期性光滑化的限幅迭代方法,求解激光核聚变中的X光能谱取得了较好的结果。这个方法适用于根据亚千X射线谱仪、多道k边滤波谱仪和多道滤波-荧光谱仪的测量结果回推靶等离子体的X射线能谱。计算结果表明,该方法完全抑制了数值不稳定性,消除了非物理的“负能谱”现象和解谱结果中的数值结构。特别是该方法对初始试探谱有很强的适应性,解谱计算结果与初始试探谱无关。 相似文献
32.
Raoul Kopelman 《Journal of statistical physics》1986,42(1-2):185-200
Heterogeneous kinetics are shown to differ drastically from homogeneous kinetics. For the elementary reaction A + A products we show that the diffusion-limited reaction rate is proportional tot
– h[A]2 or to [A]x, whereh=1- d
s/2, X=1+2/d
s
=(h-2)(h-1), andd
s
is the effective spectral dimension. We note that ford = d
s
=1, h =1/2 andX = 3, for percolating clustersd
s = 4/3,h = 1/3 andX = 5/2, while for dust ds <1, 1 >h > 1/2 and >X > 3. Scaling arguments, supercomputer simulations and experiments give a consistent picture. The interplay of energetic and geometric heterogeneity results in fractal-like kinetics and is relevant to excitation fusion experiments in porous membranes, films, and polymeric glasses. However, in isotopic mixed crystals, the geometric fractal nature (percolation clusters) dominates. 相似文献
33.
ZNF191 (243-368), a new human zinc finger protein, probably relates to some hereditary diseases and cancers, To obtain adequate amount of ZNF191(243-368) for the study of its property, structure and function, three different expression systems of inclusion-body, glutathione S-transferase (GST), and hexahistidine (6 × His) were used and compared. Among these systems, the expression level of ZNFI91(243-368) was increased in inclusion body system under a higher isopropylthio-β-D-galactoside (IPTG) concentration, but the non-target proteins were also increased more, which made its purification more difficult and the yield lower. The expression of His-tag fusion protein was almost not affected by IPTG concentration, temperature and inducing time. At a high IPTG concentration the highest expression yield for GST fusion protein was obtained. And the fusion proteins can be partially purified by a single affinity chromatography step. The fusion protein systems show advantages for expression of these proteins. 相似文献
34.
High-level expression of soluble human β-defensin-2 fused with green fluorescent protein in Escherichia coli cell-free system 总被引:2,自引:0,他引:2
Human β-defensin-2 (hBD2), a small cationic peptide, exhibits a broad range of antimicrobial activity and does not acquire
any microbial resistance. To produce this uneasily detectable, degradable, and toxic polypeptide efficiently, an alternative
approach based on the Escherichia coli cell-free biosynthesis system was proposed. The approach implies that a polypeptide of interest is synthesized as a fusion
protein linked to a green fluorescent protein (GFP) through a cleavable spacer. With batch-mode operation, a significant amount
of hBD2 fused with GFP (0.25 mg/mL) can be expressed in this cell-free system. The productivity of the fusion protein can
be improved up to 1.2 mg/mL by employing a continuous-exchange cell-free system. Furthermore, the GFP moiety provides directly
visible and quantitative monitoring of the polypeptide synthesis, and the product is soluble and stable. This work will be
helpful in allowing the rapid and visible expression of other similar defensins using an in vitro cell-free system. 相似文献
35.
36.
The cold and heat denaturations of bovine P-lactoglobulin A ((β-lg A) has been studied in solutions of guanidine hydrochloride
(GuHCI) by differential scanning calorimetry (DSC). The experimental results are presented and discussed. It is shown that
the number of protons bound by the monomeric molecules of β-lg A was unchanged before and after its heat denaturation below
pH 3, and that the activation energy of the heat denaturation was depressed owing to the presence of GuHCI. In the solutions
with 2.50 and 3.06 mol/L of GuHCI, both the cold and heat denaturations of P-lg A were observed. In comparison with the heat
denaturation, the activation energy of cold denaturation was far lower and the number of GuHCl molecules bound by the unfolded
polypeptide chains after culd denaturation increased a lot. The absolute value of the enthalpy of cold denaturation was larger
than that of heat denaturation. It was found by the analysis that the contribution to the total denaturational enthalpy of
conformational change itself of the monomeric molecules of β-lg A was the lowest among the globulins, according to the average
of the number of heavy atoms.
Project supported by the National Natural Science Foundation of China, and by the fund for excellent items under Director
of the Institute of Chemistry. 相似文献
37.
E. R. Hensema M. E. R. Sena M. H. V. Mulder C. A. Smolders 《Journal of polymer science. Part A, Polymer chemistry》1994,32(3):527-537
New aromatic poly-1,2,4-triazoles and poly-1,3,4-oxadiazoles are studied as thermally stable membrane materials. Various groups were introduced onto the pendant phenyl groups of poly-1,2,4-triazoles. Glass transition temperature, degradation temperature, and cold crystallization behavior were studied as a function of these groups. Cold crystallization appeared to be highly sensitive to macromolecular regularity. The solubility of poly-1,3,4-oxadiazoles was highly improved upon incorporation of 5-t-butylisophthalic, 1,1,3-trimethyl-3-phenylindane, 4,4′-(2,2′-diphenyl) hexafluoro propane, and diphenyl ether groups into the polymeric main chain, whereas the high glass transition temperatures and degradation temperatures typical for aromatic poly-1,3,4-oxadiazoles were maintained. © 1994 John Wiley & Sons, Inc. 相似文献
38.
The plastic deformation mechanism operating in polymer glasses is analyzed. The whole process consists of two main stages: nucleation of special shear defects, called PSTs (plastic shear transformations), and their disappearance. The important feature of plastic deformation of glasses is the storage of a large amount of internal energy ΔUdef upon straining. Such energy storage is the critical issue for mechanical performance of polymeric material: if the amount of stored energy is high, the appearance of macroscopic failure is very probable while glassy materials collecting a small amount of stored deformation energy are quite ductile. It is proposed that the rate of disappearance of PSTs is a key factor in dissipation of stored deformation energy. A parameter describing the dissipation ability of material upon deformation is introduced. 相似文献
39.
Barry R. Lentz 《Journal of fluorescence》1995,5(1):29-38
An important process in the life of a cell is fusion between cellular membranes. This is the process by which two cellular compartments surrounded by different membranes join to become a single compartment surrounded by a single membrane, without significant loss of compartment contents. To demonstrate fusion, the cell biophysicist must demonstrate all three critical aspects of the process: (1) mixing of membrane components, (2) mixing of compartment contents; and (3) retention of compartment contents. Most commonly, accomplishing this involves the use of fluorescence probes. The general theme to the methods described involves some form of concentration-dependent quenching. An unique method developed in our laboratory utilizes the concentration dependence of the fluorescence lifetime of a phosphatidylcholine containing carboxyethyl diphenylhexatriene at position 2 and palmitic acid at position 1 of glycerol (DPHpPC). The fluorescence lifetime of this molecule and that of its parent fluorophore diphenylhexatriene (DPH) shorten dramatically as their two-dimensional concentrations in a membrane increase. This lifetime quenching can be described by dimer formation that reduces the symmetry of the DPH excited state. This phenomenon allows one to use the fluorescence lifetime to gain insight into the local concentration of probe in microscopic regions of a membrane. One application of this is in distinguishing lipid transfer between the outer leaflets of two contacting membrane bilayers from fusion between these membranes that leads to mixing of lipids in both the inner and outer leaflets of the membrane bilayers. This allows a single measurement to demonstrate fusion between membrane pairs.Abbreviations PEG
poly(ethylene glycol)
- Na2EDTA
ethyiene-diamine-tetraacedic acid, disodium salt
- LUV
large, unilamellar vesicles made by rapid extrusion technique
- DPH
1,6-diphenyl-trans-1,3,5-hexatriene
- DPHpPC
1-palmitoyl-2-[[[2-[4- (phenyl-trans-1,3,5-hexatrienyl)phenyl]ethyl]oxy]carbonyl]-3-sn-phosphatidylcholine
- DPPC
1,2-dipalmitoyl-3-sn-phosphatidylcholine
- PA
palmitic acid
- NBD-PE
N-(7-nitro-2,1,3-benzoxadiazol-4-yl)-PE
- Rh-PE
N-(lissamine Rhodamine B sulfoyl)-PE
- R18
octadecyl Rhodamine B chloride
- ANTS
1-aminonaphthalene-3,6,8-trisulfonic acid
- DPX
N,N-p-xylylene-bis(pyradinium bromide) 相似文献
40.
The catalase (fromAspergillus niger) has been immobilized by a chemical method on the pous SiO2 modified with γ-aminopropyltrietoxysilane, followed with glutaraldehyde and by a physical method in alginate and γ-carrageenan
gel. Optimum support:enzyme ratios and pH values were determined for modified SiO2 in a series of immobilization reactions of catalase in the presence of the crosslinking agent glutaraldehyde, and for alginate
and γ-carrageenan in the presence of hemoglobin and bovine serum albimine. pH and temperaturedependent activity variations
and the stability properties of immobilized catalase preparations were investigated. Rate constants for H2O2 decomposition and catalase deactivation were determined. The decomposition rate of H2O2 used in the cold pasteurizatioan of milk were investigated in a discontinuous batch type reactor system. Activity half-lives
of immobilized catalase were determined. 相似文献