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基于免疫共沉淀-液质联用技术的新型孕烷X受体配体检测方法的建立
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作者 赵爽 姜棋予 +5 位作者 孙慧伟 柴燕涛 李晓娟 王志杰 侯俊 赵敏 《生物技术通讯》 CAS 2018年第3期397-403,共7页
目的:建立基于免疫共沉淀-液质联用技术的新型孕烷X受体(PXR)配体检测方法。方法:在HEK293细胞中转染带有Flag标签的PXR表达载体,裂解细胞后用偶联Flag抗体的微珠(beads)结合并分离细胞中表达的FlagPXR蛋白;以PXR的已知最为公认的配体/... 目的:建立基于免疫共沉淀-液质联用技术的新型孕烷X受体(PXR)配体检测方法。方法:在HEK293细胞中转染带有Flag标签的PXR表达载体,裂解细胞后用偶联Flag抗体的微珠(beads)结合并分离细胞中表达的FlagPXR蛋白;以PXR的已知最为公认的配体/激动剂利福平为模型药物,配制1μmol/L利福平溶液,与结合有Flag-PXR蛋白的微珠孵育形成微珠-蛋白-利福平复合物;将微珠从体系中分离出来,用蛋白印迹实验检测复合物中的蛋白质,用液相色谱-质谱联用技术(液质联用技术)检测复合物中的利福平。在此基础上对利福平的作用进行验证,在肝细胞癌细胞Hep G2中检测系列浓度梯度的利福平对PXR转录因子活性的影响。结果:用免疫共沉淀技术从HEK293细胞中分离鉴定得到Flag-PXR蛋白;用液质联用技术检测到蛋白与小分子复合物中的利福平;利福平能够剂量依赖地诱导PXR的转录因子活性。结论:建立了基于免疫共沉淀-液质联用技术的新型PXR配体检测方法。 展开更多
关键词 孕烷X受体 免疫共沉淀 蛋白-分子复合物 液质联用
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Electrochemical Tuning by Polarized UV Light Induced Molecular Orientation of Chiral Salen-type Mn(II) and Co(II) Complexes in an Albumin Matrix
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作者 Eirika Tsuda Yuya Mitsumoto +4 位作者 Kazuya Takakura Nobumitsu Sunaga Takashiro Akitsu Taro Konomi Masahiro Katoh 《Journal of Chemistry and Chemical Engineering》 2016年第2期53-59,共7页
The authors have prepared supramolecular systems as artificial metalloproteins composed of several chiral salen-type Mn(II) and Co(II) complexes in a HSA (human serum albumin) matrix. The docking was discussed b... The authors have prepared supramolecular systems as artificial metalloproteins composed of several chiral salen-type Mn(II) and Co(II) complexes in a HSA (human serum albumin) matrix. The docking was discussed by UV-vis spectral changes and a ligand-protein docking simulation program. After linearly polarized UV light irradiation, that anisotropy of molecular orientation of the complexes increased was confirmed by polarized IR spectra. The authors have observed that the electrochemical behavior of the aligned complexes incorporating diphenyl groups in HSA can be tuned without UV radiation damage of HSA higher structures. 展开更多
关键词 Redox potential Schiff base Mn(II) complex Co(II) complex albumin.
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The Biology of Chilo Iridescent Virus
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作者 Remziye Nalac1oglu Ikbal Agah Ince Zihni Demirbag 《Virologica Sinica》 SCIE CAS CSCD 2009年第4期285-294,共10页
Chilo iridescent virus (CIV) is the type species for genus Iridovirus, and belongs to the family Iridoviridae. Since the discovery of CIV in 1966, many attempts were made to elucidate the viral genome structure. The v... Chilo iridescent virus (CIV) is the type species for genus Iridovirus, and belongs to the family Iridoviridae. Since the discovery of CIV in 1966, many attempts were made to elucidate the viral genome structure. The virions contain a single linear ds DNA molecule that is circularly permuted and terminally redundant. The genome of CIV has been entirely sequenced. The CIV virion consists of an unusual three-layer structure containing an outer proteinaceous capsid, an intermediate lipid membrane, and a core DNA-protein complex containing the genome. CIV has a broad host spectrum and has, in general, a limited mortality effect on its hosts. Up to now there have been several studies about CIV describing its structure, ecology, and molecular biology. In this review study we present all these studies together to describe the CIV. 展开更多
关键词 Chilo iridescent virus IRIDOVIRUS Host range Virus replication Molecular biology
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热休克蛋白90抑制剂的研究进展 被引量:9
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作者 罗浩铭 孙薇 +1 位作者 尹建元 杨晓虹 《药学学报》 CAS CSCD 北大核心 2010年第7期813-820,共8页
热休克蛋白90(Hsp90)是抗肿瘤药物作用的新靶点,其抑制剂通过破坏体内蛋白的结构和降解过程起到抗肿瘤的作用。近年来,Hsp90抑制剂的研究不仅拘泥于对天然产物的结构改造,更多的是通过高通量筛选和计算机辅助药物设计方法进行先导化合... 热休克蛋白90(Hsp90)是抗肿瘤药物作用的新靶点,其抑制剂通过破坏体内蛋白的结构和降解过程起到抗肿瘤的作用。近年来,Hsp90抑制剂的研究不仅拘泥于对天然产物的结构改造,更多的是通过高通量筛选和计算机辅助药物设计方法进行先导化合物的发现以及合成新型结构的Hsp90抑制剂。Hsp90作为一类重要的生物学靶点在抗肿瘤药物的研制过程中越来越受到重视。本文对近年来以Hsp90为靶点的小分子抑制剂的研究进展进行综述。 展开更多
关键词 热休克蛋白90抑制剂 高通量筛选 构效关系 分子-蛋白复合物 进展
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Combination of NMR spectroscopy and X-ray crystallography offers unique advantages for elucidation of the structural basis of protein complex assembly 被引量:3
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作者 FENG Wei PAN LiFeng ZHANG MingJie 《Science China(Life Sciences)》 SCIE CAS 2011年第2期101-111,共11页
NMR spectroscopy and X-ray crystallography are two premium methods for determining the atomic structures of macro-biomolecular complexes.Each method has unique strengths and weaknesses.While the two techniques are hig... NMR spectroscopy and X-ray crystallography are two premium methods for determining the atomic structures of macro-biomolecular complexes.Each method has unique strengths and weaknesses.While the two techniques are highly complementary,they have generally been used separately to address the structure and functions of biomolecular complexes.In this review,we emphasize that the combination of NMR spectroscopy and X-ray crystallography offers unique power for elucidating the structures of complicated protein assemblies.We demonstrate,using several recent examples from our own laboratory,that the exquisite sensitivity of NMR spectroscopy in detecting the conformational properties of individual atoms in proteins and their complexes,without any prior knowledge of conformation,is highly valuable for obtaining the high quality crystals necessary for structure determination by X-ray crystallography.Thus NMR spectroscopy,in addition to answering many unique structural biology questions that can be addressed specifically by that technique,can be exceedingly powerful in modern structural biology when combined with other techniques including X-ray crystallography and cryo-electron microscopy. 展开更多
关键词 NMR spectroscopy X-ray crystallography structural biology protein complex assembly
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