荧光法研究3种黄酮化合物与牛血清白蛋白的结合作用

运用荧光光谱法研究了生理酸度条件下（pH=7.4）3种黄酮化合物白杨素、芹菜素和桑色素与牛血清白蛋白（BSA）的结合作用。结果表明,3种黄酮化合物均能与BSA形成基态复合物导致BSA内源荧光猝灭,猝灭机理为静态猝灭。结合常数K（芹菜素）〉K（白杨素）〉K（桑色素）,结合位点数近似等于1,白杨素与BSA之间以疏水作用为主,而芹菜素、桑色素与BSA之间的作用力主要是氢键和范德华力。黄酮分子结构中羟基位置及个数影响其与BSA间的结合作用,C4＇-OH对结合有促进作用,而C3-OH的取代则导致作用力减弱。由Frster非辐射能量转移理论,计算出3种黄酮化合物在蛋白质中的结合位置与212位色氨酸残基间的距离分别为2.44 nm（白杨素）、3.34 nm（芹菜素）和3.31 nm（桑色素）。     

人血清淀粉样蛋白A1原核表达及胶体金检测方法的建立

通过胶体金免疫层析技术建立一种特异、便捷、快速的SAA1定量检测新方法.利用大肠杆菌BL21(DE3)原核表达人血清淀粉样蛋白A1(SAA1),根据BL21(DE3)表达偏好性设计并合成SAA1蛋白基因片段,构建表达载体pET-28a-SAA1,采用CaCl2法制备BL21(DE3)感受态,热激转化法将pET-28a-SAA1转入到BL21(DE3).经表达条件优化,获得重组蛋白最佳诱导表达条件:温度30℃,时间6h,转速180rpm/min,培养基pH 7.0,IPTG浓度0.4mM,诱导表达后目的蛋白经SDS-PAGE电泳鉴定,Ni柱纯化、透析、浓缩从而获得浓度为8.09mg/ml,纯度为85%的SAA1.同时,结合胶体金标记技术,建立了SAA1胶体金免疫层析试纸检测方法,线性范围0.16~500μg/ml,最低检测限0.16μg/ml,该研究为临床体外诊断SAA1快速检测提供技术基础.     

A label-free amperometric immunosensor based on horseradish peroxidase functionalized carbon nanotubes and bilayer gold nanoparticles

In this work, a novel label-free amperometric immunosensor has been constructed for detecting α-1-fetoprotein (AFP) based on nanocomposite of horseradish peroxidase (HRP) labeled carbon nanotubes (CNTs). First, the gold nanoparticles (AuNPs) were electrodeposited on the surface of the glass carbon electrode by electrochemical reduction of gold chloride tetrahydrate (HAuCl₄) to immobilize horseradish peroxidase labeled carbon nanotubes (HRP-CNTs). Then HRP-CNTs bioconjugate was immobilized on the surface of the electrodeposited AuNPs layer by the combination of forces (coordination and electrostatic force). Subsequently, it was immersed into gold colloidal nanoparticles (GNPs) solution, which was used to immobilize antibody biomolecules (anti-AFP). Enhanced sensitivity was obtained by using bioconjugates featuring HRP labeled (HRP-CNTs), which had lager specific surface area and good electronic catalysis (current response signal) compared to carbon nanotubes. Under optimized conditions, the linear ranges were from 0.2 to 200 ng mL⁻¹ with a detection limit of 0.067 ng mL⁻¹ (at an S/N of 3). The proposed immunosenor showed good precision, acceptable stability and reproducibility and could be used for the detection AFP in normal human serum, which provided a potential alternative tool for the detection of protein in clinical diagnosis.     

不同品系北京鸭血清前白蛋白多态性的研究

应用聚丙烯酰胺凝胶电泳法研究了北京鸭的血清前白蛋多态性,在2个位点观察到多态,Pam位点为单态,在Pas位点发现有5种表现型,它们的频率是：Pas2-2O 26．67％,Pas1-2为12％,Pas2-1为45.33%,Pas1-1为2．67％,Pas2-0为13．33％,在Paf位点发现有4种表现型,它们的频率是：PafF为29．33％,PafS为41．33％,PafFS为10．67％,Paf0为18．67％,并计算了它们的基因频率,群体平均杂合度和遗传距离,遗传分析表明,樱桃谷鸭和奥白星鸭遗传结构相似,而与B系北京鸭遗传结构有明显差异。     

抗狂犬病血清致过敏反应及血清病的探讨

128例犬咬伤患者注射抗狂犬病血清后,过敏反应发生率为3.91％(5/128);血清病发生率为11.72％(15/128)。过敏反应的主要症状为头晕、恶心、面色苍白;血清病的主要症状为局部及周身荨麻疹、表浅淋巴结肿大、恶心、食欲不振等。血清病有明显的年龄特点,0～19岁儿童和青少年发生率为4.0％,20岁以上成年人为13.59％,二者差异显著。     

糖-蛋白质饮料对男力量运动员一次抗阻运动后部分血清指标的影响

为探讨糖-蛋白质补充对一次性抗阻运动恢复过程的影响.文中以18名男子力量项目运动员在一次抗阻运动前、运动中和运动后,分别摄入糖-高蛋白饮料(HP组=6人,糖:蛋白质=3∶1)、糖-低蛋白饮料(LP组=6人,糖∶蛋白质=6∶1)或纯糖对照饮料(C组=6人).在运动前、运动后即刻、运动后3h和运动后次日晨采集血样,测定血清肌酸激酶(CK)、天门冬氨酸转移酶(AST)、谷丙氨酸转移酶(ALT)、尿素(BU)以及睾酮(T)和皮质醇(Cor).研究结果表明:运动后3h和运动后次日晨C组CK水平显非常著高于HP组和LP组(P0.01,分别),运动后次日晨LP组CK水平显著高于HP组(P0.05);运动后3hC组ALT水平显著高于HP组和LP组(P0.05,分别);运动后即刻C组Cor水平显著低于HP组和LP组(P0.05,分别);各时间点T、AST及BU水平组间比较无差异性.摄入糖-蛋白质饮料能促进男性力量项目运动员抗阻运动后机体运动能力的恢复和提高.摄入糖-高比例蛋白质更有利于运动后疲劳的恢复和机体运动能力的提高.     

压电式传感器测定蛋白质吸附动力学参数

利用液隔电极型压电式传感器实时监测牛血清白蛋白(BSA)在石英表面吸附过程。基于所提出的吸附动力学模型,估算出BSA在石英表面的吸附速率常数为ka=1.27×103mol-1·L·s-1,脱附速率常数为kd=1.31×10-3s-1,由可逆吸附态向不可逆吸附态的转化速率常数为kf=3.46×10-4s-1。     

磁场对大鼠血清营养相关生化指标的影响

报道了旋转恒定磁场对大鼠血液生化指标的影响.在强度为0 4T,旋转速率为8Hz的磁场条件下,鼠龄3周的大鼠,磁场每天处理2h,共持续10周,导致血清葡萄糖水平显著下降;鼠龄为10周的大鼠,每天磁场处理2h,共持续4周,则引起血清甘油三酯水平的显著降低,血清高密度脂蛋白水平则显著上升.     

Electroseparation of an antibacterial peptide fraction from snow crab by-products hydrolysate by electrodialysis with ultrafiltration membranes

Recently, a snow crab by-products hydrolysate has demonstrated antibacterial properties due to a peptide with a molecular weight of about 800 Da, but only at high concentration. Consequently, peptide hydrolysate has been fractionated to obtain peptides in a more purified form. The aim of this work was to separate a snow crab by-products hydrolysate by electrodialysis with ultrafiltration membranes (EDUF). EDUF, which allows separation of molecules according to their charges and molecular weights, was used to recover and concentrate the active antibacterial fraction. Two different ultrafiltration membranes (20 and 50 kDa) and two electrical field strengths (2 and 14 V/cm) were used as separation parameters. After EDUF separation, the 300-600 Da peptide molecular weight range was the most recovered with an abundance of 94%. Moreover, fractionation at 14 V/cm with ultrafiltration membranes of 50 kDa allowed the recovery of an anionic fraction which showed antibacterial properties on Escherichia coli ATCC 25922 and Listeria innocua HPB 13.     

Proteomics in the Diagnosis of Endometriosis: Opportunities and Challenges

The non‐surgical diagnosis of endometriosis is still challenging for the clinician. Ultrasonography and magnetic resonance imaging can be used to diagnose ovarian endometriotic cysts and deep infiltrating endometriosis; but their performance is poor in the diagnosis of initial stages of endometriosis. CA‐125 and other serum markers (such as CA 19‐9, serum protein PP14, interleukins, and angiogenetic factors) have been measured in women with endometriosis but they are not reliable for the diagnosis of the disease. Although several studies used proteomics technologies to identify plasmatic markers of endometriosis, the non‐invasive diagnosis of endometriosis is far from being achieved. In this issue, Manousopoulou et al. compare the integrated quantitative proteomic profile of eutopic endometrium and serum of women with endometriosis and controls. 1214 proteins are differentially expressed in the eutopic endometrium and 404 proteins in the serum of the two study groups. 21 proteins are aberrantly expressed in both eutopic endometrium and serum of women with endometriosis. More work is needed to assess if the differentially expressed proteins identified in this study can be used as clinical markers of endometriosis.