单电极直流电弧炉电热特性理论研究

运用电磁理论与流体静压力原理,导出了电弧自身的电磁向心压缩力以及电弧对熔池冲力的解析式。又运用辐射传热原理,导出了单电极电弧对熔池与炉衬辐射传热的解析式。解析式揭示出电弧自身电磁向心压缩力、电弧对熔池冲力,单电极电弧对熔池以及对炉衬辐射传热的规律。     

Prediction of the structure of a receptor-protein complex using a binary docking method.

To validate procedures of rational drug design, it is important to develop computational methods that predict binding sites between a protein and a ligand molecule. Many small molecules have been tested using such programs, but examination of protein-protein and peptide-protein interactions has been sparse. We were able to test such applications once the structures of both the maltose-binding protein (MBP) and the ligand-binding domain of the aspartate receptor, which binds MBP, became available. Here we predict the binding site of MBP to its receptor using a 'binary docking' technique in which two MBP octapeptide sequences containing mutations that eliminate maltose chemotaxis are independently docked to the receptor. The peptides in the docked solutions superimpose on their original positions in the structure of MBP and allow the formation of an MBP-receptor complex. The consistency of the computational and biological results supports this approach for predicting protein-protein and peptide-protein interactions.     

Short alanine-based peptides may form 3(10)-helices and not alpha-helices in aqueous solution.

Short alanine peptides, containing 16 or 17 residues, appear to form alpha-helices in aqueous solution. But the main spectroscopic analyses used on helical peptides (circular dichroism and nuclear magnetic resonance) cannot distinguish between an alpha-helix (in which the ith residue is hydrogen-bonded to residue i + 4; ref. 9) and the next most common peptide helix, the 3(10)-helix10 (i-->i + 3 hydrogen-bonding). To address this problem we have designed single and doubly spin-labelled analogues of alanine-based peptides in which the nitroxide spin label forms an unbranched side chain extending from the sulphur atom of a cysteine residue. Here we report the circular dichroism, Fourier-transform infrared and electron-spin resonance spectra of these peptides under helix-forming conditions. The infrared absorbance gives an amide I' band with a frequency that is substantially different from that observed for alpha-helices. The electron-spin resonance spectra of doubly labelled helices show that the ranking of distances between side chains, around a single turn (residues 4-8), is inconsistent with an alpha-helical structure. Our experiments suggest that the more likely peptide geometry is a 3(10)-helix.     

我国跨国经营的发展构想

本文在系统阐述当代跨国经营战略调整与发展趋势的基础上，简要剖析了现阶段我国企业跨国经营的主要问题，重点探讨了我国跨国企业发展战略的基本构想。     

SDP协议的应用分析

SDP协议是在IETF MMUSIC工作组的RFC2327中定义的一个多媒体会话描述协议，本文介绍了SDP协议的功能，分析了SDP协议格式，语法结构及解释，同时给出了一些应用实例。     

均匀设计─灰色联合预测及其应用─邮发期刊价格预测

本文利用均匀设计优化参数估计，建立了较精确的图书馆工作的灰色模型；并预测了今后数年的期刊价格发展趋势。     

A calcium sensor in the sodium channel modulates cardiac excitability.

Sodium channels are principal molecular determinants responsible for myocardial conduction and maintenance of the cardiac rhythm. Calcium ions (Ca2+) have a fundamental role in the coupling of cardiac myocyte excitation and contraction, yet mechanisms whereby intracellular Ca2+ may directly modulate Na channel function have yet to be identified. Here we show that calmodulin (CaM), a ubiquitous Ca2+-sensing protein, binds to the carboxy-terminal 'IQ' domain of the human cardiac Na channel (hH1) in a Ca2+-dependent manner. This binding interaction significantly enhances slow inactivation-a channel-gating process linked to life-threatening idiopathic ventricular arrhythmias. Mutations targeted to the IQ domain disrupted CaM binding and eliminated Ca2+/CaM-dependent slow inactivation, whereas the gating effects of Ca2+/CaM were restored by intracellular application of a peptide modelled after the IQ domain. A naturally occurring mutation (A1924T) in the IQ domain altered hH1 function in a manner characteristic of the Brugada arrhythmia syndrome, but at the same time inhibited slow inactivation induced by Ca2+/CaM, yielding a clinically benign (arrhythmia free) phenotype.     

苦丁茶与常用茶中微量元素分析

苦丁茶又称苦丁、苦簦、皋卢等 ,是我国南方和东南亚地区常饮的代用茶 .几千年民间饮用和现代医学验证苦丁茶具有清热解毒、杀菌消炎、活血脉、降血脂、降胆固醇等功效 .近 10年来 ,科技人员对苦丁茶的化学成分进行了多方面的研究 ,确定其中含有化学成分达 2 0 0多种[1] ,一部分与普通茶叶相同 ,如咖啡碱、多酚类、儿茶素、氨基酸等 ,但含量比普通茶叶低[2 ] ,此外 ,苦丁茶还含有熊果酸 (Ｕｒｓｏｌｉｃ ａｃｉｄ)、β 香树脂醇 (β Ａｍｙｒｉｎ)、蛇麻脂醇 (Ｌｕｐｅｏｌ)、熊果醇 (Ｕｖａｏｌ)和 β 谷甾醇 (β Ｓｉｓｔｅｒｏｌ)等 .但…     

云南臭参的研究现状和开发构想

介绍了有关臭参挥发性臭味的化学成分 ,臭参的化学成分、药效学和急性毒性动物实验、临床实验、营养成分测定、药理学研究等研究现状 .提出了科研及产品开发构想 .     

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.

The fragile-X syndrome is the most frequent inherited form of mental retardation, with an incidence of 1 in 1,500 males. It is characterized by the presence of a fragile site at Xq27.3 induced in vitro by folate deprivation or by inhibitors of deoxynucleotide synthesis. Its mode of inheritance is unusual for an X-linked trait, with incomplete penetrance in both males and females. Some phenotypically normal males transmit the mutation to all their daughters who rarely express any symptoms, but penetrance is high in sons and daughters of these carrier women. Genetic and physical mapping of the Xq27-q28 region has confirmed that the disease locus is located at or very near the fragile site. Hypotheses proposed to account for the abnormalities in the inheritance of the disease include sequence rearrangements by meiotic recombination or a mutation that affects reactivation of an inactive X chromosome during differentiation of female germ cells. To detect such rearrangements, or methylation changes that may reflect a locally inactive X chromosome, we used pulsed-field gel analysis of DNA from fragile-X patients with probes close to the fragile-X locus. The probe Do33 (DXS465) detected abnormal patterns in fragile-X patients, but not in normal controls or in non-expressing male transmitters.