期刊文献+
共找到8篇文章
< 1 >
每页显示 20 50 100
高性能胰蛋白酶分子表面印迹材料的制备及其大分子识别特性研究
1
作者 陈涛 门吉英 高保娇 《化学研究与应用》 CAS CSCD 北大核心 2016年第5期636-643,共8页
以交联聚乙烯醇(CPVA)微球为基质,以甲基丙烯酸(MAA)为功能单体,在中性水介质中制备了高性能胰蛋白酶(TRY)大分子表面印迹材料。首先通过CPVA微球表面的羟基与甲基丙烯酰氯之间的酯化反应,将大量可聚合双键甲基丙烯酰基(MAO)引入微球表... 以交联聚乙烯醇(CPVA)微球为基质,以甲基丙烯酸(MAA)为功能单体,在中性水介质中制备了高性能胰蛋白酶(TRY)大分子表面印迹材料。首先通过CPVA微球表面的羟基与甲基丙烯酰氯之间的酯化反应,将大量可聚合双键甲基丙烯酰基(MAO)引入微球表面,获得改性微球MAO-CPVA。在中性水溶液中,单体MAA的羧基几乎发生完全电离,凭借强烈的静电相互作用,MAA自动结合在碱性蛋白TRY大分子周围,形成单体-模板复合体。水溶液中过硫酸铵/亚硫酸氢钠引发体系所产生的自由剂,使包围在TRY周围的单体MAA与交联剂N,N'-亚甲基双丙烯酰胺(MBA)在微球MAO-CPVA表面发生接枝交联聚合,而模板TRY则被包裹在交联网络之中,除去模板后便得到了TRY表面印迹微球MIP-PMAA/CPVA。深入考察了该表面印迹微球的大分子识别性能。研究结果表明,表面印迹微球MIP-PMAA/CPVA对TRY具有优良的结合亲和性,结合容量高达84mg·g^(-1)(3.6μmol·g^(-1));对模板蛋白TRY具有特异的识别选择性,相对于另一种碱性蛋白木瓜蛋白酶,印迹微球对TRY的选择性系数高达21.62。 展开更多
关键词 胰蛋白酶 甲基丙烯酸 表面印迹 碱性蛋白质 大分子识别
下载PDF
牛血清白蛋白分子表面印迹材料的制备及其大分子识别特性研究 被引量:3
2
作者 史楠 高保娇 陈涛 《高分子学报》 SCIE CAS CSCD 北大核心 2014年第12期1678-1686,共9页
通过分子设计和过程策划,制备了高性能的牛血清白蛋白(BSA)分子表面印迹材料.首先以甲基丙烯酰氯为试剂,使交联聚乙烯醇(CPVA)微球表面的羟基发生酯化反应,将大量可聚合双键引入到CPVA微球表面.然后以含有可聚合双键的CPVA微球为载体,... 通过分子设计和过程策划,制备了高性能的牛血清白蛋白(BSA)分子表面印迹材料.首先以甲基丙烯酰氯为试剂,使交联聚乙烯醇(CPVA)微球表面的羟基发生酯化反应,将大量可聚合双键引入到CPVA微球表面.然后以含有可聚合双键的CPVA微球为载体,阳离子单体丙烯酰氧乙基三甲基氯化铵(DAC)为功能单体,N,N'-亚甲基双丙烯酰胺(MBA)为交联剂,牛血清白蛋白(BSA)为模板分子,在水溶液体系中,基于主-客体之间的强静电相互作用,采用接枝聚合与印迹过程同步进行的方式,制备了高性能BSA分子表面印迹微球MIP-PDAC/CPVA.采用红外光谱(IR)和扫描电子显微镜(SEM)对产物微球进行了表征.研究了印迹聚合物微球MIP-PDAC/CPVA对BSA的大分子识别特性.研究结果表明,微球MIP-PDAC/CPVA对BSA具有优良的结合亲和性和特异的识别选择性,结合容量高达108 mg/g,对牛血红蛋白(BHb)却基本不结合;相对于BHb,MIP-PDAC/CPVA对BSA的选择性系数高达60.2. 展开更多
关键词 牛血清白蛋白 丙烯酰氧乙基三甲基氯化铵 表面印迹 接枝聚合 大分子识别
原文传递
胰蛋白酶分子表面印迹材料的制备及其大分子识别特性
3
作者 陈涛 史楠 +1 位作者 门吉英 高保娇 《过程工程学报》 CAS CSCD 北大核心 2016年第2期272-278,共7页
以交联聚乙烯醇(CPVA)微球为基质,采用接枝聚合和表面印迹同步技术制备碱性蛋白胰蛋白酶(TRY)分子表面印迹材料,甲基丙烯酰氯与CPVA微球表面的羟基发生快速酯化反应,得到表面含大量可聚合双键甲基丙烯酰基(MAO)的改性微球MAO-CPVA.按一... 以交联聚乙烯醇(CPVA)微球为基质,采用接枝聚合和表面印迹同步技术制备碱性蛋白胰蛋白酶(TRY)分子表面印迹材料,甲基丙烯酰氯与CPVA微球表面的羟基发生快速酯化反应,得到表面含大量可聚合双键甲基丙烯酰基(MAO)的改性微球MAO-CPVA.按一定摩尔比将TRY和单体阴离子单体对苯乙烯磺酸钠(SSS)溶解在水溶液中,加入交联剂N,N'-亚甲基双丙烯酰胺(MBA),MAO-CPVA分散于水介质中,过硫酸铵/亚硫酸氢钠引发体系产生自由基,使包围在TRY周围的单体SSS与MBA在MAO-CPVA表面发生接枝交联聚合,制得TRY表面印迹微球MIP-PSSS/CPVA,对其进行表征,考察了其大分子识别性能.结果表明,MIP-PSSS/CPVA对TRY有优良的亲和性和特异识别选择性,吸附容量达85.9 mg/g,对TRY的选择性系数相对于蛋白溶菌酶LZM达17.52. 展开更多
关键词 胰蛋白酶 印迹聚合物 微球 对苯乙烯磺酸钠 吸附 大分子识别
原文传递
生物大分子纳米孔分析技术研究进展 被引量:7
4
作者 丁克俭 张海燕 +3 位作者 胡红刚 赵红敏 关伟军 马月辉 《分析化学》 SCIE EI CAS CSCD 北大核心 2010年第2期280-285,共6页
脱氧核糖核酸穿越纳米孔动力学研究以及利用纳米孔开展新型DNA测序技术研究是后人类基因组计划的热点之一。本文对生物纳米孔、固态纳米孔以及纳米孔生物大分子识别技术的研究现状进行了归纳和总结,并对该领域的发展趋势进行展望。
关键词 纳米孔 溶血素蛋白 生物大分子识别 综述
下载PDF
Factor analysis identifies subgroups of constipation 被引量:3
5
作者 Philip G Dinning Mike Jones +6 位作者 Linda Hunt Sergio E Fuentealba Jamshid Kalanter Denis W King David Z Lubowski Nicholas J Talley Ian J Cook 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第11期1468-1474,共7页
AIM:To determine whether distinct symptom groupings exist in a constipated population and whether such grouping might correlate with quantifiable pathophysiological measures of colonic dysfunction.METHODS:One hundred ... AIM:To determine whether distinct symptom groupings exist in a constipated population and whether such grouping might correlate with quantifiable pathophysiological measures of colonic dysfunction.METHODS:One hundred and ninety-one patients presenting to a Gastroenterology clinic with constipation and 32 constipated patients responding to a newspaper advertisement completed a 53-item,wide-ranging selfreport questionnaire.One hundred of these patients had colonic transit measured scintigraphically.Factor analysis determined whether constipation-related symptoms grouped into distinct aspects of symptomatology.Cluster analysis was used to determine whether indi-vidual patients naturally group into distinct subtypes.RESULTS:Cluster analysis yielded a 4 cluster solution with the presence or absence of pain and laxative unresponsiveness providing the main descriptors.Amongst all clusters there was a considerable proportion of patients with demonstrable delayed colon transit,irritable bowel syndrome positive criteria and regular stool frequency.The majority of patients with these characteristics also reported regular laxative use.CONCLUSION:Factor analysis identified four constipation subgroups,based on severity and laxative unresponsiveness,in a constipated population.However,clear stratification into clinically identifiable groups remains imprecise. 展开更多
关键词 Factor analysis CONSTIPATION SYMPTOMS CLUSTERS LAXATIVES
下载PDF
Bio-inspired enantioseparation for chiral compounds
6
作者 Yan Fu Jinjin Yang +1 位作者 Jinli Zhang Wei Li 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2016年第1期31-38,共8页
Biomacromolecules including protein and nucleic acids are considered as promising chiral selectors in the fields of enantioselective separation, owing to their inherent chirality, polymorphous structures, stable physi... Biomacromolecules including protein and nucleic acids are considered as promising chiral selectors in the fields of enantioselective separation, owing to their inherent chirality, polymorphous structures, stable physicochemical properties, good biocompatibility as well as susceptible modification and regulation. In this review, firstly,enantioselective recognition mechanism of proteins and nucleic acids toward different enantiomers is discussed,as well as their potential applications on the chiral separation of racemic compounds. Secondly, preparative enantioseparation adopting biomolecule-modified hybrid materials including porous microspheres, magnetic nanoparticles and affinity membranes, are introduced respectively. Finally, novel chiroptical materials constructed on the basis of chiral induction, transfer, amplification and transcription, are recognized as promising candidates in future applications. 展开更多
关键词 Chirality Enantioseparation Protein DNA
下载PDF
Applications of pillarenes, an emerging class of synthetic macrocycles 被引量:1
7
作者 SONG Nan YANG Ying-Wei 《Science China Chemistry》 SCIE EI CAS 2014年第9期1185-1198,共14页
Synthetic macrocycles, a typical type of building block for molecular recognition and self-assembly, are crucial to supramolecular chemistry and materials science. Since 2008, a new generation of synthetic macrocyclic... Synthetic macrocycles, a typical type of building block for molecular recognition and self-assembly, are crucial to supramolecular chemistry and materials science. Since 2008, a new generation of synthetic macrocyclic hosts, pillarenes and their abundant derivatives, which consist of hydroquinone units linked by methylene bridges at 2,5-positions, have been the focus of much research. Numerous studies on their host-guest properties and the fabrication of supramolecular assemblies have demon- strated that pillarenes and their derivatives possess many advantages that facilitate their applications in many research fields. Herein we summarize and classitfy the applications of pillarenes in terms of artificial transmembrane channels, controlled delivery systems, dispersion of carbon hybrid materials, extraction and absorption, liquid crystals, metal-organic frameworks, sensing and detection, stabilization of nanoparticles (Au/Ag/CdTe), and other typical biological applications. We also provide an overview of future developments in pillarene chemistry. 展开更多
关键词 drug delivery host-guest interactions macrocycles pillarenes supramolecular materials
原文传递
Recent advances in target identification by natural product based chemical probes
8
作者 Benke Hong Ting Dong Xiaoguang Lei 《Science China Chemistry》 SCIE EI CAS CSCD 2016年第9期1088-1092,共5页
Natural products have been extensively used to treat diseases throughout human history. These are mainly because natural products normally target biological macromolecules selectively. Target identification could help... Natural products have been extensively used to treat diseases throughout human history. These are mainly because natural products normally target biological macromolecules selectively. Target identification could help us to develop new therapeutic agents and discover new biological pathways underlying human diseases. Herein, we highlight some recent examples of using natural products and their derivatives as chemical probes to identify the molecular targets and elucidate mode of action. 展开更多
关键词 natural product chemical probe chemical biology target ID
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部