Fritzsche W, Vesenka J, Henderson E
Department of Zoology and Genetics, Iowa State University, Ames 50011, USA.
Scanning Microsc. 1995 Sep;9(3):729-37; discussion 738-9.
Scanning force microscopy (SFM) is a new method to obtain the topography of surfaces with nanometer-resolution. The ability to image under liquids makes the technique attractive for biological applications, especially for the determination of the ultrastructure of biomolecules under native conditions. One growing field of interest is the investigation of chromatin and chromatin-related structures. Different levels of chromatin condensation were the subject of several previous SFM investigations, from the nucleosomal chain, to the 30-nm fiber, ending with the metaphase chromosome. The SFM yielded new information on such fundamental problems as the core spacing of the nucleosomal chain, the internal structure of the 30-nm fiber and the banding mechanism of metaphase chromosomes. Other investigations dealt with the SFM characterization of polytene chromosomes. This paper reviews the state-of-the-art in SFM chromatin research and discusses future developments in this field.
扫描力显微镜(SFM)是一种用于获取具有纳米分辨率的表面形貌的新方法。在液体环境下成像的能力使该技术在生物学应用中颇具吸引力,特别是对于在天然条件下测定生物分子的超微结构。一个日益受到关注的领域是对染色质及染色质相关结构的研究。先前的几项SFM研究以不同程度的染色质凝聚为主题,从核小体链到30纳米纤维,直至中期染色体。SFM在诸如核小体链的核心间距、30纳米纤维的内部结构以及中期染色体的带型机制等基本问题上提供了新信息。其他研究则涉及多线染色体的SFM表征。本文综述了SFM染色质研究的现状,并讨论了该领域的未来发展。