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单分子水平高分子相互作用的AFM成像与单分子力谱研究
引用本文:张文科.单分子水平高分子相互作用的AFM成像与单分子力谱研究[J].高分子学报,2011(9):913-922.
作者姓名:张文科
作者单位:吉林大学化学学院超分子结构与材料国家重点实验室 长春130012
摘    要:结合作者近期的研究工作,重点介绍了如何把原子力显微镜(AFM)成像及单分子力谱结合(包括原位结合或者离位结合)起来,研究高分子之间的相互作用.本文涉及生物高分子(主要是核酸-蛋白质体系)以及合成高分子体系(如聚氧乙烯,PEO)的相关研究工作.对于生物高分子体系,主要以长链核酸(如双螺旋DNA及RNA)为探针,首先利用A...

关 键 词:原子力显微镜  单分子力谱  核酸-蛋白质相互作用  聚合物单晶

AFM IMAGING AND SINGLE-MOLECULE FORCE SPECTROSCOPY STUDIES ON MACROMOLECULAR INTERACTIONS AT SINGLE-MOLECULE LEVEL
ZHANG Wenke.AFM IMAGING AND SINGLE-MOLECULE FORCE SPECTROSCOPY STUDIES ON MACROMOLECULAR INTERACTIONS AT SINGLE-MOLECULE LEVEL[J].Acta Polymerica Sinica,2011(9):913-922.
Authors:ZHANG Wenke
Abstract:The investigations on macromolecular interactions at the single-molecule level using atomic force microscopy(AFM) imaging and AFM-based single-molecule force spectroscopy(SMFS),with an emphasis on the combination of these two methods,have been discussed on the base of the author's recent work in related fields.First,AFM imaging(including static air phase and in situ liquid phase AFM imaging) is used to detect the effect of protein-binding on the topology of double stranded DNA(dsDNA) based on the characteristic(spaghetti-like) AFM image of dsDNA.Then,SMFS study on the nature of force-induced conformation transition of dsDNA is demonstrated.The force-fingerprint of dsDNA can then be used to study protein-DNA interactions revealing the effects of protein-binding on the dynamic conformation of dsDNA.In addition,the application of AFM-based SMFS in the investigation of RNA-protein coat interactions in an intact plant virus,tobacco mosaic virus(TMV),has been demonstrated.To realize this,a TMV particle is immobilized perpendicularly on a gold-coated substrate.The genetic RNA can then be pulled step-by-step out of the TMV particle through its 5′ opening.This study extends the force spectroscopy technique to the investigation of nucleic acid-protein interactions in more complicated biological systems(i.e.,in the virus particle).Finally,the attempt in the quantitative study of polymer interactions in a polyethylene oxide(PEO) single crystal is successfully accomplished by pulling a single PEO chain via its thiol-labelled end out of its single crystal by a good in situ combination of AFM imaging and SMFS.The generality of the established method in the investigation of crystallization of other polymers is discussed.This quantitative information on inter-and intramolecular interactions of macromolecules is useful in revealing the mechanism of many important biological processes(such as DNA replication) as well as in the design of high-performance polymer materials.
Keywords:Atomic force microscopy  Single-molecule force spectroscopy  Nucleic acid-protein interaction  Polymer single crystal
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