Resolution enhancement techniques in microscopy

被引:0
作者
Christoph Cremer
Barry R. Masters
机构
[1] Superresolution Microscopy,
[2] Institute of Molecular Biology (IMB),undefined
[3] Kirchhoff Institute of Physics (KIP),undefined
[4] University Heidelberg,undefined
[5] Department of the History of Science,undefined
[6] Harvard University,undefined
[7] Department of Biological Engineering,undefined
[8] Massachusetts Institute of Technology,undefined
来源
The European Physical Journal H | 2013年 / 38卷
关键词
Point Spread Function; Optical Resolution; Resolution Enhancement; Localization Microscopy; Optical Transfer Function;
D O I
暂无
中图分类号
学科分类号
摘要
We survey the history of resolution enhancement techniques in microscopy and their impact on current research in biomedicine. Often these techniques are labeled superresolution, or enhanced resolution microscopy, or light-optical nanoscopy. First, we introduce the development of diffraction theory in its relation to enhanced resolution; then we explore the foundations of resolution as expounded by the astronomers and the physicists and describe the conditions for which they apply. Then we elucidate Ernst Abbe’s theory of optical formation in the microscope, and its experimental verification and dissemination to the world wide microscope communities. Second, we describe and compare the early techniques that can enhance the resolution of the microscope. Third, we present the historical development of various techniques that substantially enhance the optical resolution of the light microscope. These enhanced resolution techniques in their modern form constitute an active area of research with seminal applications in biology and medicine. Our historical survey of the field of resolution enhancement uncovers many examples of reinvention, rediscovery, and independent invention and development of similar proposals, concepts, techniques, and instruments. Attribution of credit is therefore confounded by the fact that for understandable reasons authors stress the achievements from their own research groups and sometimes obfuscate their contributions and the prior art of others. In some cases, attribution of credit is also made more complex by the fact that long term developments are difficult to allocate to a specific individual because of the many mutual connections often existing between sometimes fiercely competing, sometimes strongly collaborating groups. Since applications in biology and medicine have been a major driving force in the development of resolution enhancing approaches, we focus on the contribution of enhanced resolution to these fields.
引用
收藏
页码:281 / 344
页数:63
相关论文
共 875 条
  • [1] Abbe E.(1873)Beiträge zur Theorie des Mikroskops und der mikroskopischen Wahrnehmung. M Schultze’s Archive für Mikroskopische Anatomie IX 413-468
  • [2] Agard D.A.(1983)Three-dimensional architecture of a polytene nucleus Nature 302 676-681
  • [3] Sedat J.(1835)On the Diffraction of an Object-glass with Circular Aperture Trans. Cambridge Philos. Soc. 5 283-291
  • [4] Airy G.B.(2001)Spatially modulated illumination microscopy: online visualization of intensity distribution and prediction of nanometer precision of axial distance measurements by computer simulations Journal of Biomedical Optics 6 292-292
  • [5] Albrecht B.A.(2002)Spatially modulated illumination microscopy allows axial distance resolution in the nanometer range Appl. Opt. 41 80-87
  • [6] Failla V.(2008)Photoswitchable fluorescent proteins enable monochromatic multilabel imaging and dual color fluorescence nanoscopy Nature Biotechnology 26 1035-1040
  • [7] Heintzmann R.(1972)Super-resolution aperture scanning microscope Nature 237 510-512
  • [8] Cremer C.(2006)4Pi microscopy deconvolution with a variable point-spread function Appl. Optics 45 7056-7064
  • [9] Albrecht B.A.(2007)Nanostructure analysis using spatially modulated illumination microscopy Nature Protocols 2 2640-2646
  • [10] Failla A.(2009)Light-induced dark states of organic fluorochromes enable 30 nm resolution imaging in standard media Biophys. J. 96 L22-L24