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冯喜增, 刘涛, 陈龙, 侯森, 薛永来, 冯喜增*
科学通报,2006,51(4):399~403,-0001,():
-1年11月30日
设计并制备了一种新的具有分子探针功能的主体分子型非病毒载体-邻菲啰啉-β-环糊精衍生物主体分子(DZY-1),应用凝胶电泳法研究探讨了DZY-1与DNA相互作用及客体分子对该主体分子诱导DNA凝聚的影响;并进一步研究探讨了单一主体分子、主/客体分子配合物诱导DNA分子凝聚和聚合所形成的超分子聚合物抗限制性内切酶(HindⅢ)酶解的特性. 应用扫描电子显微镜(SEM)观测到该主体分子、主/客体分子配合物与DNA分子相互作用形成超分子聚合物的微观结构形态。阐述了其作为非病毒基因载体可能的传递机制,为设计、制备新的非病毒基因载体提供了一种新途径。
邻菲啰啉-β-环糊精衍生物, λ-非病毒基因载体, 凝胶电泳, 扫描电子显微镜
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冯喜增, 王立凯冯喜增*
化学进展,2005,12(3):482~498,-0001,():
-1年11月30日
微流控芯片最初起源于分析化学领域,是一种采用精细加工技术,在数平方厘米的基片,制作出微通道网络结构及其它功能单元,以实现集微量样品制备、进样、反应、分离及检测于一体的快速、高效、低耗的微型分析实验装置。随着微电子及微机械制作技术的不断进步,近年来微流控芯片技术发展迅猛,并开始在化学、生命科学及医学器件等领域发挥重要作用。本文首先简单介绍了微流控芯片制作材料和工艺,然后主要阐述了其在蛋白质分离、免疫分析、NDA分析和测序、细胞培养及检测等方面的应用进展。
微流控芯片免疫分析, DNA分析, 细胞培养
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冯喜增, Xizeng Feng, Clive J. Roberts, * David A. Armitage, Martyn C. Davies, Saul J. B. Tendler, Stephanie Allen and Philip M. Williams
Analyst, 2001, 126, 1100-1104,-0001,():
-1年11月30日
Selective plasma treatment of the recessed regions of the elastomer stamps is shown to alter the resultant protein patterns. Fluorescence microscopy is demonstrated to be an excellent tool to discriminate between regions of microcontact printed fluorescent dye-labelled albumin in polystyrene. Atomic force microscopy and shear force microscopy are used to provide high-resolution images of the patterned protein layers. The formation and characteristics of the patterns formed by these alternative strategies is discussed.
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冯喜增, Haijun Zhou, Yang Zhang, Zhong-can Ou-Yang, Stuart M. Lindsay, Xi-Z. Feng, , Pichumani Balagurumoorthy and Rodney E. Harrington*
J. Mol. Biol.(2001)306, 227-238,-0001,():
-1年11月30日
The tumor-suppressor activity of p53 is closely related to its DNA-binding properties. It binds a number of DNA response-elements and it is likely that these share a common structural feature. Here, we present a new, general method to determine the absolute twist of exible DNA promoter sequences based on direct imaging of the topology of microcircles containing the sequences. We have used magnetically driven dynamic force microscopy ("MacMode" AFM) to observe, in solution, the conformation of 168 base-pair DNA microcircles, each containing four equally spaced copies of the waf1/cip1/p21 p53 response-element. Analysis of the images showed that the microcircles are markedly puckered with a small excess of negatively writhed molecules. The average measured values of writhe are 0.109 0.013 (for 60 positively writhed molecules) and 0.098 0.011 (for 65 negatively writhed molecules). These values lead directly to a difference in linking number for the positively and negatively writhed molecules prior to ligation, from which we derive a twist mismatch of 178 (overtwist). This is 44.5 for each 42-mer precursor containing a single waf1/cip1/p21 p53 response-element, in good agreement with the range of values deduced by indirect biochemical techniques. The two values of writhe may also be used to determine the ratio of the bending (B) to twisting (C) rigidity, yielding B/C 0.23. This is about one-third of the value for long, random-sequence DNA, suggesting that the waf1/cip1/p21 p53 response-element is extremely exible, a result that is also consistent with indirect biochemical experiments. These results support the idea, proposed by us earlier, that torsional stress may play a role in the regulation of p53 binding through modulation of twist at the binding site.
p53, waf1DNAresponse-element, DNAmicrocircle, MacModeatomicforcemicroscopy, *, Correspondingauthorwrithe
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