期刊文献+

原子力显微镜对生理溶液中活细胞成像条件的研究 被引量:5

Study on the basic conditions affecting the atomic force microscopic observation of the living cells in physical solutions
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摘要 本文研究用原子力显微技术(AFM)在生理条件下对活细胞成像的基本方法,并对各种影响成像因素如针尖与细胞表面的非特异性相互作用、AFM悬臂弹性系数及细胞表面柔性等问题提供相应的解决方案。从而为AFM在成像的基础上对活细胞其它性质的研究提供基础。用本文方法清晰地显示了固定细胞与活细胞膜表面所具有的明显差别:活细胞膜完整平滑,固定细胞表面粗糙,边缘不整。 The basic methods to image living cells in physiological solutions with atomic force microscope (AFM) and various factors that affect the quality of the image have been studied. These factors include the non-specific interactions between the AFM tip and the surface of the cells, the elastic constant of the cantilever, the softness of the cells and so on. Several ways have been proposed to solve the problems often encountered in AFM imaging of the living cells in physiological solutions, which provided basis for the studies on the other surfacial properties of the living cells. With the method reported in this paper, the membrane surface of the living cells can be clearly distincted from that of the fixed cells. The membrane of the living cells is intact and smooth while that of the fixed cells is rough and incomplete at their margin.
出处 《电子显微学报》 CAS CSCD 2005年第1期79-84,共6页 Journal of Chinese Electron Microscopy Society
基金 国家自然科学基金资助项目(No 30271501). ~~
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参考文献8

  • 1Kim H,Arakawa H,Osada T,Ikai A. Quantification of cell adhension force with AFM:distribution of vitronectin receptors on a living MC3T3-E1 cell [J].Ultramicroscopy, 2003,97: 359-363.
  • 2Iikai A, Afrin R, Itoh A, Thogersen H C, Hayashi Y, Osada T. Force measurements for membarne protein manipulation[J]. Colloids and Surface B: Biointerfaces, 2002,23 (2 ~3) :165-171.
  • 3Kada G, Blayney L, Jeyakumar L H, Kienberger F,Pastushenko V Ph, Fleischer S, Schindler H, Lai F A,Hinterdorfer P. Recognition force microscopy/spectroscopy of ion channels: applications to the skeletal muscle Ca2+release channel[J] . Ultramicroscopy, 2001,86: 129-137.
  • 4Lehenkari P P, Horton M A. Singal integrin molecule adhension force in intact cells measured by atomic foece microscopy [J]. Biochemical and Biophysical Research Communications, 1999,259: 645-650.
  • 5Lee I, Marchant R E. Molecular interaction studies of hemostasis: fibrinogen ligand-human platelet receptor interaction [J]. Ultramicroscopy, 2003,97: 341-352.
  • 6Yuan C B,Chen A,Kolb P,Moy V T. Energy landscape of streptavidin-biotin complexes measured by atomic force microscopy [J]. Biochemistry, 2000,39: 10219-10223.
  • 7Grandbois M, Dettmann W, Benoit M, Gaub H E. Affinity imaging of red blood cells using an atomic force microscope[J]. Journal of Histochemistry and Cytochemistry, 2000,48:719-724.
  • 8韩立,韩冬,王秀凤,陈皓明.扫描探针显微镜进行细胞扫描时探针对于细胞活性的影响[J].电子显微学报,2003,22(2):92-96. 被引量:6

二级参考文献3

  • 1Colton Richard J,Baselt David R,Dufrêne Yves F,Green John-Bruce D ,Lee Gil U. Scanning probe microscopy[J]. Chemical Biology,1997,l1(3):370-3 77.
  • 2Catherine G Galbraith,Michael P Sheetz. Forces on adhesive contacts a ffect cell function[J]. Cell Biology,1998,10:566-571.
  • 3赵清亮,王景贺,李旦,董申.扫描探针显微镜的最新技术进展及应用[J].电子显微学报,2000,19(1):69-75. 被引量:13

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