交叉视差及观看时间对自由立体显示视觉舒适度的影响

针对自由立体显示器视疲劳的问题,对交叉视差及观看时间影响视觉舒适度的问题进行了分析和研究。实验选取具有交叉视差的图片和视频,观察者采用主观评价和客观评价相结合的方法,对其观看舒适度进行评价。结果表明具有交叉视差的图片和视频,其观看舒适度都随时间的增加而减弱,图片的观看时间应在23min以内,视频的观看时间应在17min以内,此时观看较为舒适。持续观看具有交叉视差的图片和视频会引起视疲劳,应控制其观看时间。     

基于鱼眼投影的头戴显示器全景显示系统

设计了一套结合鱼眼摄像头和头戴显示器的新型全景显示系统。采用鱼眼正交投影法建立合适的数学模型,基于该数学模型合理展开虚拟半球的UV,将鱼眼图像映射到虚拟半球上,同时使用双目虚拟摄像头采集已经矫正畸变的图像,并将其显示在头戴显示器中,达到头戴显示器全景显示的效果。通过实际测试验证了该方案的可行性。     

基于虚拟仪器技术和网络的综合实验控制系统设计

为实现大型物理实验现场复杂多样的仪器控制,分析了物理实验的特点、过程、环境及仪器控制功能需求,利用虚拟仪器技术、计算机网络技术和数据库技术,建立了一套集成硬件和软件的综合控制管理信息系统,实现记录系统中示波器状态远程批量设置及波形数据自动采集、控制探测系统的高压电源并发加压或退压、保障各测试项目间测试仪器之间时间关联、监控UPS电量和远端现场图片或视频状态。给出了系统的关键的设计思路,列举了某型示波器控制的通用控制代码。结果表明,系统达到了一人总控或多人分权控制实验过程中多种多台仪器的目标,方便快捷地实现不同品牌不同类型示波器的相同功能。     

Large-scale differential display analysis of T helper cell differentiation

We have developed a novel large-scale multicapillary fluorescent differential display (FDD) platform amenable to further automation. The power of the method is demonstrated by the analysis of T helper cell differentiation. Eight RNA samples from wild type, Stat4 knockout and Stat6 knockout mice were analyzed with 16 anchoring primers and 24 arbitrary primers, resulting in 285 294 sample peaks. Visually selected patterns of differential expression suggest two major regulatory mechanisms: activation and Stat4 genotype. A subset of the findings is reproduced in the confirmatory differential display (DD) that included technical and biological replicates. In a small fragment identification pilot study, we identify Ifi27 and Cct8 to be up-regulated by T cell activation. We present a method for the analysis of electropherogram similarity across large datasets, based on correlation of low-resolution representations of electrophoretic data. We show how it can be applied to analyze experimental and technical variables. Using this method, we demonstrate the effect of activation and genotype. In addition, agreement of our real experimental data to the theoretical basis of DD, as well as issues in anchoring primer selectivity, are studied.     

Differential display identifies genes in chinese hamster ovary cells sensitive to elevated ammonium

Ammonium is a toxic waste product that has been reported to negatively inhibit cell growth and recombinant glycosylation in Chinese hamster ovary (CHO) cells; however, the effect of this toxicity on intracellular gene expression has received only limited investigation. We used a differential display method to identify genes in CHO cells that were affected by ammonium stress. Eight genes whose mRNA levels significantly changed in response to elevated ammonium were isolated and identified. Five of the genes were identified as having lower expression under the ammonium stress, whereas three genes were identified as having higher expression. Sequence homology with other mammalian organisms was used to attribute function to these newly identified genes. The identified ammonium-sensitive genes were grouped into three broad functional groups: cellular processes, energy metabolism, and genetic-information processing. The three cellular process-related genes had lower expression (anaphase-promoting complex subunit 5, eukaryotic initiation factor 5A II, KIAA1091 protein). The two energy-related genes had higher expression under ammonium stress (adenosine triphosphate synthase subunit C and mitofusin 1). Both of the genetic information-processing genes (endoplasmic reticulum [ER]-resident protein ERdj5 and structure-specific recognition protein 1) had lower expression under the ammonium stress, whereas the 26S proteasome subunit adenosine triphosphatase 3 gene had higher expression. These preliminary results indicate that ammonium stress lowers expression of genes controlling cell cycle, protein folding, and quality and raises genes that control energy metabolism and degradation. Our findings demonstrate the usefulness of mRNA differential-display techniques for the detection of CHO cell genes affected by ammonium stress.     

Influence of electronic and steric effects on stability constants and electrochemical reversibility of divalent ion complexes with glycine and sarcosine. A glass electrode potentiometric, sampled direct current polarographic, virtual potentiometric, and molecular modelling study

Cd^II complexes with glycine (gly) and sarcosine (sar) were studied by glass electrode potentiometry, direct current polarography, virtual potentiometry, and molecular modelling. The electrochemically reversible Cd^II–glycine–OH labile system was best described by a model consisting of M(HL), ML, ML₂, ML₃, ML(OH) and ML₂(OH) (M = Cd^II, L = gly) with the overall stability constants, as log β, determined to be 10.30 ± 0.05, 4.21 ± 0.03, 7.30 ± 0.05, 9.84 ± 0.04, 8.9 ± 0.1, and 10.75 ± 0.10, respectively. In case of the electrochemically quasi-reversible Cd^II–sarcosine–OH labile system, only ML, ML₂ and ML₃ (M = Cd^II, L = sar) were found and their stability constants, as log β, were determined to be 3.80 ± 0.03, 6.91 ± 0.07, and 8.9 ± 0.4, respectively. Stability constants for the ML complexes, the prime focus of this work, were thus established with an uncertainty smaller than 0.05 log units. The observed departure from electrochemical reversibility for the Cd–sarcosine–OH system was attributed mainly to the decrease in the transfer coefficient . The MM2 force field, supplemented by additional parameters, reproduced the reported crystal structures of diaqua-bis(glycinato-O,N)nickel(II) and fac-tri(glycinato)-nickelate(II) very well. These parameters were used to predict structures of all possible isomers of (i) [Ni(H₂O)₄(gly)]⁺ and [Ni(H₂O)₄(sar)]⁺; and (ii) [Ni(H₂O)₃(IDA)] and [Ni(H₂O)₃(MIDA)] (IDA = iminodiacetic acid, MIDA = N-methyl iminodiacetic acid) by molecular mechanics/simulated annealing methods. The change in strain energy, ΔU_str, that accompanies the substitution of one ligand by another (ML + L′ → ML′ + L), was computed and a strain energy ΔU_str = +0.28 kcal mol⁻¹ for the reaction [Ni(H₂O)₄(gly)]⁺ + sar → [Ni(H₂O)₄(sar)]⁺ + gly was found. This predicts the monoglycine complex to be marginally more stable. By contrast, for the reaction [Ni(H₂O)₃IDA] + MIDA → [Ni(H₂O)₃MIDA] + IDA, ΔU_str = −0.64 kcal mol⁻¹, and the monoMIDA complex is predicted to be more stable. This correlates well with (i) stability constants for Cd–gly and Cd–sar reported here; and (ii) known stability constants of ML complex for glycine, sarcosine, IDA, and MIDA.     

用于增强现实的头盔显示器的设计

穿透式双通道头盔显示器 (HMD)是增强现实系统中的关键部件。本文给出了一种新颖的穿透式双通道头盔显示器的设计方案 ,使得当在用于增强现实系统中时 ,能够获得更大的透过率 ,以获得清晰的外部世界与内部产生的场景信息。同时通过成功的光学设计 ,获得了大视场、高分辨率的光学系统     

电路参数对外电极气体放电过程影响的计算机分析

本文通过对外电极气体放电物理过程的计算机模拟,研究了一些主要电学参量(包括电源电压、外电路阻抗、介质层电容和介质层上的壁电荷等)对放电过程的影响.文中给出了关于放电电流、辐射亮度和电功损耗等项放电特性随外电路阻抗变化的一维数值分析实例.     

悬浮法生产可发性聚苯乙烯(EPS)虚拟仿真实验平台的设计与开发

为实现我校高分子材料与工程专业人才培养目标,即培养高素质工程应用型人才,弥补教学过程中实际操作的缺陷与不足,我们开发了基于实际工业生产的悬浮法生产可发性聚苯乙烯的虚拟仿真实验平台.详述了该平台的设计开发思路与理念,平台主题结构,以及实验主控界面设计思路和主要内容.实践证明,该平台不仅包含工程应用的相关知识,而且极大的提...     

A Phage Display-Identified Short Peptide Capable of Hydrolyzing Calcium Pyrophosphate Crystals—The Etiological Factor of Chondrocalcinosis

Chondrocalcinosis is a metabolic disease caused by the presence of calcium pyrophosphate dihydrate crystals in the synovial fluid. The goal of our endeavor was to find out whether short peptides could be used as a dissolving factor for such crystals. In order to identify peptides able to dissolve crystals of calcium pyrophosphate, we screened through a random library of peptides using a phage display. The first screening was designed to select phages able to bind the acidic part of alendronic acid (pyrophosphate analog). The second was a catalytic assay in the presence of crystals. The best-performing peptides were subsequently chemically synthesized and rechecked for catalytic properties. One peptide, named R25, turned out to possess some hydrolytic activity toward crystals. Its catalysis is Mg²⁺-dependent and also works against soluble species of pyrophosphate.