多维标度线性回归技术应用于人体血清临床指标的FTIR光谱定量分析

人体血清临床指标是衡量人体健康和亚健康水平的重要因素之一,采用傅里叶红外(FTIR)光谱技术实现人体血清临床指标的多成分快速同时检测。提出利用多维标度法(MDS)对光谱变量进行降维,结合多元线性回归(MLR)技术,建立多维标度线性回归(MDS-MLR)模型,为血清四种临床生化指标(葡萄糖、低密度脂蛋白胆固醇、甘油三酯、尿素)的定量分析优选光谱信息波长点,优化定标预测模型,结合移动平均法(MA)进行光谱预处理,得到良好的建模效果。通过检验集样品进行验证,检验相关系数均在0.9以上。结果表明,MDS-MLR方法具有人体血清临床指标FTIR光谱分析的应用潜力。FTIR技术结合MDS-MLR定量分析方法可以实现对人体健康和亚健康水平的快速评定。     

人血清白蛋白和牛血清白蛋白荧光量子产率的测量

以L-色氨酸荧光量子产率0．14为标准,测量了人血清白蛋白和牛血清白蛋白水溶液在不同激发波长下的荧光量子产率。在pH6．4和25℃条件下,人血清白蛋白和牛血清白蛋白在最大激发波长280nm的荧光量子产率分别为0．132和0．130。实验发现,pH对蛋白质荧光强度有明显影响,溶解氧对荧光量子产率基本没有影响。     

某煤矿地区人发中微量元素含量与疾病关系的分析与研究

用电感耦合等离子发射光谱法(ICP-AES)测定并统计了甘肃兰州窑街煤矿地区228例人发样中微量元素(Zn,Fe,Cu,Ca,Mn)的分布情况,测定的平均值(μg·g~(-1))为:Zn,116.1;Fe,43.3;Cu,14.6;Mn,2.08;Ca,1314。对年龄、性别、疾病对人体中这些元素的分布影响进行分析研究。根据所测人发中微量元素含量数据运用主成分分析法对厌食儿童和健康儿童进行了聚类分析研究。     

Study of Protein–Probe Interaction and Protective Action of Surfactant Sodium Dodecyl Sulphate in Urea-Denatured HSA using Charge Transfer Fluorescence Probe Methyl Ester of N,N-Dimethylamino Naphthyl Acrylic Acid

We have demonstrated that the intramolecular charge transfer (ICT) probe Methyl ester of N,N-dimethylamino naphthyl acrylic acid (MDMANA) serves as an efficient reporter of the proteinous microenvironment of Human Serum Albumin (HSA). This work reports the binding phenomenon of MDMANA with HSA and spectral modulation thereupon. The extent of binding and free energy change for complexation reaction along with efficient fluorescence resonance energy transfer from Trp-214 of HSA to MDMANA indicates strong binding between probe and protein. Fluorescence anisotropy, red edge excitation shift, acrylamide quenching and time resolved measurements corroborate the binding nature of the probe with protein and predicts that the probe molecule is located at the hydrophobic site of the protein HSA. Due to the strong binding ability of MDMANA with HSA, it is successfully utilized for the study of stabilizing action of anionic surfactant Sodium Dodecyl Sulphate to the unfolding and folding of protein with denaturant urea in concentration range 1M to 9M.     

Measurement of glutathione in human brain at 3T using an improved double quantum filter in vivo

A single voxel proton NMR double quantum filter (DQF) for measurement of glutathione (GSH) in human brain at 3T is reported. Yield enhancement for the CH₂ resonances of the cysteine moiety at 2.95 ppm has been achieved by means of dual encoding. After the preparation of double quantum and zero quantum coherences (DQC and ZQC) at equal magnitude, the first DQC encoding was followed by interchange of DQC and ZQC, and another DQC encoding. The multi-quantum coherences were fully utilized to generate a GSH target signal at 2.95 ppm. The optimal echo time and the editing efficiency were obtained with numerical analysis of the filtering performance and phantom measurements. The dual-DQC encoding method provided GSH yield greater by a factor of 2.1 than single-DQC encoding for identical slice-selective RF pulses in phantom tests. Using the phantom relaxation times and the ratio of edited GSH to N-acetylaspartate (NAA) 2.0-ppm peak areas, the concentration of GSH in the medial parietal cortex of the healthy human brain in vivo was estimated to be 1.0 ± 0.3 mM (mean ± SD, n = 7), with reference to NAA at 10 mM.     

Toxicity of nano- and micro-sized ZnO particles in human lung epithelial cells

This is the first comprehensive study to evaluate the cytotoxicity, biochemical mechanisms of toxicity, and oxidative DNA damage caused by exposing human bronchoalveolar carcinoma-derived cells (A549) to 70 and 420 nm ZnO particles. Particles of either size significantly reduced cell viability in a dose- and time-dependent manner within a rather narrow dosage range. Particle mass-based dosimetry and particle-specific surface area-based dosimetry yielded two distinct patterns of cytotoxicity in both 70 and 420 nm ZnO particles. Elevated levels of reactive oxygen species (ROS) resulted in intracellular oxidative stress, lipid peroxidation, cell membrane leakage, and oxidative DNA damage. The protective effect of N-acetylcysteine on ZnO-induced cytotoxicity further implicated oxidative stress in the cytotoxicity. Free Zn²⁺ and metal impurities were not major contributors of ROS induction as indicated by limited free Zn²⁺ cytotoxicity, extent of Zn²⁺ dissociation in the cell culture medium, and inductively-coupled plasma-mass spectrometry metal analysis. We conclude that (1) exposure to both sizes of ZnO particles leads to dose- and time-dependent cytotoxicity reflected in oxidative stress, lipid peroxidation, cell membrane damage, and oxidative DNA damage, (2) ZnO particles exhibit a much steeper dose–response pattern unseen in other metal oxides, and (3) neither free Zn²⁺ nor metal impurity in the ZnO particle samples is the cause of cytotoxicity.     

Synthesis of nano hydroxyapatite powder that simulate teeth particle morphology and composition

A simple sol–gel precipitation technique to synthesize nano hydroxyapatite (HA) particles (30 nm) that show similar morphology, size and crystallinity to HA crystals of human teeth is reported. Calcium nitrate tetrahydrate and potassium dihydrogenphosphate were used as calcium and phosphorus precursors, respectively. Double distilled water was used as a diluting media for HA sol preparation and ammonia was used to adjust the pH to 11. After aging, the HA gel was dried at 40 °C and calcined to different temperatures ranging from 200 to 600 °C. The dried and calcined powders were characterized for phase composition using X-ray diffractrometry, and Fourier transform infra-red spectroscopy. The particle size and morphology was studied using Transmission electron microscopy. The particle size distribution analysis of HA powders showed skewed distribution plot. The phase and particle characterization studied above showed that HA calcined at 600 °C simulate HA crystals of teeth.     

光谱法测定伊曲康唑与牛血清和人血清白蛋白相互作用

用荧光光谱和紫外吸收光谱法, 在pH=7.4±0.1的0.1 mol·L-1磷酸缓冲溶液中, 研究了伊曲康唑与牛血清白蛋白(BSA)和人血清白蛋白(HSA)的相互作用. 实验结果表明, 伊曲康唑与牛血清白蛋白和人血清白蛋白作用的猝灭常数均随着温度的升高而降低, 伊曲康唑可以有规律地使血清白蛋白内源荧光猝灭, 其猝灭机理可认为是伊曲康唑与白蛋白形成复合物的静态猝灭. 获得了在不同温度下, 伊曲康唑与血清白蛋白作用的结合常数以及△G、△H和△S等热力学参数. 根据所得结果可推断伊曲康唑与白蛋白的作用力主要为疏水作用力, 同时, 利用荧光共振能量转移理论(FRET)计算得出了伊曲康唑与白蛋白结合位置的距离d. 而且, 利用同步荧光光谱和紫外光谱揭示了该反应中蛋白的结构和其微环境的变化.     

人类免疫缺陷病毒整合酶二酮酸类抑制剂的三维药效团构建

应用遗传算法相似性程序(GASP), 以作用于I型人类免疫缺陷病毒(human immun-odeficiency virus type 1, HIV-1)整合酶(IN)的二酮酸类(diketoacids, DKAs)抑制剂构建药效团模型. 所选训练集分子均具有可靠的类药性特征及DKAs药效团特征. 尝试将抑制剂与药效团叠合后的构象和抑制剂与IN的对接构象进行叠合, 得到药效团模型与分子对接构象中IN残基的相对位置, 并基于抑制剂的药效团模型特征与周围IN氨基酸残基位置的匹配情况进行药效团特征的修改. 所得最优药效团由1个疏水特征、3对氢键特征和1个氢键供体特征组成. 该药效团的命中物质量(goodness of hit, GH)为0.56, 产出率(Y)达63.6%, 假阳性率(FP)为0.41%. 该药效团具有较好的置信度, 产出率较高而假阳性率较低, 可用于数据库搜索发现新的具有DKAs药效团特征的活性化合物, 也可为先导化合物的改造提供帮助.     

Surface modified capillary electrophoresis combined with in solution isoelectric focusing and MALDI-TOF/TOF MS: A gel-free multidimensional electrophoresis approach for proteomic profiling—Exemplified on human follicular fluid

Development of miniaturized analytical tools continues to be of great interest to face the challenges in proteomic analysis of complex biological samples such as human body fluids. In the light of these challenges, special emphasis is put on the speed and simplicity of newly designed technological approaches as well as the need for cost efficiency and low sample consumption. In this study, we present an alternative multidimensional bottom-up approach for proteomic profiling for fast, efficient and sensitive protein analysis in complex biological matrices. The presented setup was based on sample pre-fractionation using microscale in solution isoelectric focusing (IEF) followed by tryptic digestion and subsequent capillary electrophoresis (CE) coupled off-line to matrix assisted laser desorption/ionization time of flight tandem mass spectrometry (MALDI TOF MS/MS). For high performance CE-separation, PolyE-323 modified capillaries were applied to minimize analyte–wall interactions. The potential of the analytical setup was demonstrated on human follicular fluid (hFF) representing a typical complex human body fluid with clinical implication. The obtained results show significant identification of 73 unique proteins (identified at 95% significance level), including mostly acute phase proteins but also protein identities that are well known to be extensively involved in follicular development.