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AC LiWang JJ Cao H Zheng Z Lu SC Peiper PJ LiWang 《Canadian Metallurgical Quarterly》1999,38(1):442-453
Encoded by Kaposi's sarcoma-associated herpesvirus, viral macrophage-inflammatory protein-II (VMIP-II) is unique among CC chemokines in that it has been shown to bind to the CXC chemokine receptor CXCR4 as well as to a variety of CC chemokine receptors. This unique binding ability allows vMIP-II to block infection by a wide range of human immunodeficiency virus type I (HIV-1) strains, but the structural and dynamic basis for this broad range of binding is not known. 15N T1, T2 and 15N[-HN] nuclear Overhauser effect (NOE) values of vMIP-II, determined through a series of heteronuclear multidimensional nuclear magnetic resonance (NMR) experiments, were used to obtain information about the backbone dynamics of the protein. Whereas almost all chemokine structures reveal a dimer or multimer, vMIP-II has a rotational correlation time (tauc) of 4.7 +/- 0.3 ns, which is consistent with a monomeric chemokine. The rotational diffusion anisotropy, D parallel/D perpendicular, is approximately 1.5 +/- 0.1. The conformation of vMIP-II is quite similar to other known chemokines, containing an unstructured N-terminus followed by an ordered turn, three beta-strands arranged in an antiparallel fashion, and one C-terminal alpha-helix that lies across the beta-strands. Most of the protein is well-ordered on a picosecond time scale, with an average order parameter S2 (excluding the N-terminal 13 amino acids) of 0.83 +/- 0. 09, and with even greater order in regions of secondary structure. The NMR data reveal that the N-terminus, which in other chemokines has been implicated in receptor binding, extends like a flexible tail in solution and possesses no secondary structure. The region of the ordered turn, including residues 25-28, experiences conformational exchange dynamics. The implications of these NMR data to the broad receptor binding capability of vMIP-II are discussed. 相似文献
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渣油悬浮床加氢裂化水溶性催化剂的研究 总被引:14,自引:2,他引:12
采用悬浮床加氢技术和水溶性分散催化剂对辽河坨子里稠油的常压渣油进行了轻质化和改质研究。对催化剂金属组成、催化剂应用条件和过程生焦及转化率的关系进行了系统考察,试验结果经数学处理后得到各关系曲线。研究结果表明,在催化剂加入量250μg/g、反应温度435℃、反应空速1.0h-1和10MPa条件下单程通过反应处理坨子里常压渣油得到轻柴油和减压馏分油的质量收率分别为31.2%及40.7%。 相似文献
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This paper investigated the glow discharge plasma electrolysis (GDPE) of methanol solutions for hydrogen generation. It is known that H2 and HCHO are the dominant products of methanol decomposition during GDPE. The experimental results indicate that high-energy electrons are the most important species to initiate methanol decomposition. Likewise, it was shown that discharged polarity, discharged voltage, and methanol concentration have important influences on hydrogen yield, energy consumption, hydrogen concentration, and hydrogen and formaldehyde output. The hydrogen yield (G(H2)) of cathodic GDPE (CGDPE) was found to be higher than that of anodic GDPE (AGDPE). In addition, the hydrogen concentration in liberated gas from CGDPE remains above 88% after the separation of HCHO when the applied voltage is higher than 750 V. The energy consumption (Wr) of CGDPE is significantly less than AGDPE. Furthermore, Wr decreased with the increase in discharged voltage, while G(H2) increased with methanol concentration. The experimental results show that the GDPE of methanol solutions is a promising technique for the simultaneous production of hydrogen and formaldehyde. 相似文献
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工作质量控制被认为是很有用的一种质量方法,是保证符合质量要求的一种有价值的途径。它是一种有计划的工作过程检查以及对产品或服务缺陷的投诉,以确定是否符合工作过程的某些程序。本文描述了如何建立一个积极的改进的工作质量控制体系,以确保质量体系持续的适应性和有效性。 相似文献
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Chemokines (chemotactic cytokines) are a family of immune system proteins, several of which have been shown to block human immunodeficiency virus (HIV) infection in various cell types. While the solved structures of most chemokines reveal protein dimers, evidence has accumulated for the biological activity of individual chemokine monomers, and a debate has arisen regarding the biological role of the chemokine dimer. Concurrent with this debate, several N-terminal truncations and modifications in the CC subfamily of chemokines have been shown to have functional significance, in many cases antagonizing their respective receptors and in some cases retaining the ability to block HIV entry to the cell. As the dimer interface of CC chemokines is located at their N-terminus, a structural study of N-terminally truncated chemokines will address the effect that this type of mutation has on the dimer-monomer equilibrium. We have studied the structural consequences of N-terminal truncation in macrophage inflammatory protein 1 beta (MIP-1 beta), a CC chemokine that has been shown to block HIV infection. Examination of nuclear magnetic resonance (NMR) spectra of a series of N-terminally truncated MIP-1 beta variants reveals that these proteins possess a range of ability to dimerize. A mutant beginning at amino acid Asp6 [termed MIP(6)] has near wild-type dimer properties, while further truncation results in weakened dimer affinity. The mutant MIP(9) (beginning with amino acid Thr9) has been found to exist solely as a folded monomer. Relaxation measurements yield a rotational correlation time of 8.6 +/- 0.1 ns for wild-type MIP-1 beta and 4.5 +/- 0.1 ns for the MIP(9) mutant, consistent with a wild-type dimer and a fully monomeric MIP(9) variant. The presence of physiological salt concentration drastically changes the monomer-dimer equilibrium for both wild-type and most mutant proteins, heavily favoring the dimeric form of the protein. These results have implications for structure-function analysis of existing chemokine mutants as well as for the larger debate regarding the biological existence and activity of the chemokine dimer. 相似文献
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