整合素-ICAM-1相互作用的二维反应动力学研究

<正>_2整合素(LFA-1和Mac-1)与其配体细胞间粘附分子-1(ICAM-1)的相互作用在诸如肿瘤转移、炎症反应等许多病理生理过程中起着重要的作用。研究表明,中性粒细胞(PMN)在特定环境下可通过_2整合素与ICAM-1的相互作用而增强黑色素瘤细胞的转移能力,但是其动力学调控机制还不清楚。受体-配体键结合和解离的二维反应动力学定量描述了分子结合的快慢和强弱,是回答_2整合素与ICAM-1相互作用如何调

千烟洲人工林主要树种地上生物量的估算

利用不同参数和函数,模拟了千烟洲人工林主要树种马尾松、湿地松和杉木的枝条、叶生物量和总生物量及单株各器官生物量,选择最佳函数计算生物量在各树种不同器官中的分配,估算不同林型的地上生物量.结果表明,不同树种的枝条基径(d)和枝条生物量(BW)、叶生物量(LW)之间,当d3为自变量时,相关系数最高,湿地松利用线性函数、马尾松和杉木利用幂函数模拟效果最佳;单木总生物量以利用D2H(胸径2×树高)为自变量的幂函数模拟相关系数最高;3个树种叶和枝生物量各有不同的最佳自变量和函数类型,但同一树种的叶、枝生物量最佳拟合方程的自变量和函数类型一致.马尾松林、湿地松林和杉木林的地上生物量分别为83·6、72·1和59t·hm-2,其中树干生物量所占比重最大,叶生物量最小.根据前人的研究结果推算3种林分地下生物量分别为10·44、9·42和11·48t·hm-2,其固碳量分别为47·94、45·14和37·52t·hm-2.

Histone modifications within the human X centromere region.

Human centromeres are multi-megabase regions of highly ordered arrays of alpha satellite DNA that are separated from chromosome arms by unordered alpha satellite monomers and other repetitive elements. Complexities in assembling such large repetitive regions have limited detailed studies of centromeric chromatin organization. However, a genomic map of the human X centromere has provided new opportunities to explore genomic architecture of a complex locus. We used ChIP to examine the distribution of modified histones within centromere regions of multiple X chromosomes. Methylation of H3 at lysine 4 coincided with DXZ1 higher order alpha satellite, the site of CENP-A localization. Heterochromatic histone modifications were distributed across the 400-500 kb pericentromeric regions. The large arrays of alpha satellite and gamma satellite DNA were enriched for both euchromatic and heterochromatic modifications, implying that some pericentromeric repeats have multiple chromatin characteristics. Partial truncation of the X centromere resulted in reduction in the size of the CENP-A/Cenp-A domain and increased heterochromatic modifications in the flanking pericentromere. Although the deletion removed approximately 1/3 of centromeric DNA, the ratio of CENP-A to alpha satellite array size was maintained in the same proportion, suggesting that a limited, but defined linear region of the centromeric DNA is necessary for kinetochore assembly. Our results indicate that the human X centromere contains multiple types of chromatin, is organized similarly to smaller eukaryotic centromeres, and responds to structural changes by expanding or contracting domains.

A planar inductively coupled radio-frequency magnetic neutral loop discharge

A planar inductively coupled radio-frequency (rf) magnetic neutral loop discharge has been designed. It provides diagnostic access to both the main plasma production region as well as a remote plane for applications. Three coaxial coils are arranged to generate a specially designed inhomogeneous magnetic field structure with vanishing field along a ring in the discharge-the so-called neutral loop (NL). The plasma is generated by applying an oscillating rf electric field along the NL, induced through a four-turn, planar antenna operated at 13.56 MHz. Electron density and temperature measurements are performed under various parameter variations. Collisionless electron heating in the NL region allows plasma operation at comparatively low pressures, down to 10(-2) Pa, with a degree of ionization in the order of several per cent. Conventional plasma operation in inductive mode without applying the magnetic field is less efficient, in particular in the low pressure regime where the plasma cannot be sustained without magnetic fields.

PURIFICATION AND PARTIAL CHARACTERIZATION OF AN ENDO-POLYGALACTURONASE FROM ASPERGILLUS NIGER

A pectinase was identified and isolated from a commercial Aspergillus niger pectinase preparation. The crude enzyme preparation, which was prepared by precipitation of the water extract of the culture of A. niger with ammonium sulfate, was further fractionated by three steps of chromatography, i. e., cation exchange, hydrophobic interaction and onion exchange, to obtain an electrophoretically homogeneous pectinase. The molecular weight of the purified enzyme was estimated by SDS-PAGE to be about 40.4 kDa under both nonreducing and reducing conditions, with the optimum pH at 5.0 and the optimum temperature at 36C. The enzyme was stable at temperatures below 35C. The partial N-terminal ammo acid sequence data analysis of the first 19 amina acids of the obtained pectinase revealed 94.7% and 89.5% homology with two reported pectinases from A. niger.