Test Samples for Optimizing STORM Super-Resolution Microscopy

被引:30
作者
Metcalf, Daniel J. [1 ]
Edwards, Rebecca [1 ]
Kumarswami, Neelam [1 ]
Knight, Alex E. [1 ]
机构
[1] Natl Phys Lab, Analyt Sci Div, Bethesda, MD USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2013年 / 79期
关键词
Molecular Biology; Issue; 79; Genetics; Bioengineering; Biomedical Engineering; Biophysics; Basic Protocols; HeLa Cells; Actin Cytoskeleton; Coated Vesicles; Receptor; Epidermal Growth Factor; Actins; Fluorescence; Endocytosis; Microscopy; STORM; super-resolution microscopy; nanoscopy; cell biology; fluorescence microscopy; test samples; resolution; actin filaments; fiducial markers; epidermal growth factor; cell; imaging;
D O I
10.3791/50579
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
STORM is a recently developed super-resolution microscopy technique with up to 10 times better resolution than standard fluorescence microscopy techniques. However, as the image is acquired in a very different way than normal, by building up an image molecule-by-molecule, there are some significant challenges for users in trying to optimize their image acquisition. In order to aid this process and gain more insight into how STORM works we present the preparation of 3 test samples and the methodology of acquiring and processing STORM super-resolution images with typical resolutions of between 30-50 nm. By combining the test samples with the use of the freely available rainSTORM processing software it is possible to obtain a great deal of information about image quality and resolution. Using these metrics it is then possible to optimize the imaging procedure from the optics, to sample preparation, dye choice, buffer conditions, and image acquisition settings. We also show examples of some common problems that result in poor image quality, such as lateral drift, where the sample moves during image acquisition and density related problems resulting in the 'mislocalization' phenomenon.
引用
收藏
页数:17
相关论文
共 48 条
[11]   Carbocyanine dyes as efficient reversible single-molecule optical switch [J].
Heilemann, M ;
Margeat, E ;
Kasper, R ;
Sauer, M ;
Tinnefeld, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (11) :3801-3806
[12]   Subdiffraction-resolution fluorescence imaging with conventional fluorescent probes [J].
Heilemann, Mike ;
van de Linde, Sebastian ;
Schuttpelz, Mark ;
Kasper, Robert ;
Seefeldt, Britta ;
Mukherjee, Anindita ;
Tinnefeld, Philip ;
Sauer, Markus .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (33) :6172-6176
[13]   Super-Resolution Imaging with Small Organic Fluorophores [J].
Heilemann, Mike ;
van de Linde, Sebastian ;
Mukherjee, Anindita ;
Sauer, Markits .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (37) :6903-6908
[14]   QuickPALM: 3D real-time photoactivation nanoscopy image processing in ImageJ [J].
Henriques, Ricardo ;
Lelek, Mickael ;
Fornasiero, Eugenio F. ;
Valtorta, Flavia ;
Zimmer, Christophe ;
Mhlanga, Musa M. .
NATURE METHODS, 2010, 7 (05) :339-340
[15]   Dynamic clustered distribution of hemagglutinin resolved at 40 nm in living cell membranes discriminates between raft theories [J].
Hess, Samuel T. ;
Gould, Travis J. ;
Gudheti, Manasa V. ;
Maas, Sarah A. ;
Mills, Kevin D. ;
Zimmerberg, Joshua .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (44) :17370-17375
[16]   Ultra-high resolution imaging by fluorescence photoactivation localization microscopy [J].
Hess, Samuel T. ;
Girirajan, Thanu P. K. ;
Mason, Michael D. .
BIOPHYSICAL JOURNAL, 2006, 91 (11) :4258-4272
[17]   Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins [J].
Hofmann, M ;
Eggeling, C ;
Jakobs, S ;
Hell, SW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (49) :17565-17569
[18]   DAOSTORM: an algorithm for high-density super-resolution microscopy [J].
Holden, Seamus J. ;
Uphoff, Stephan ;
Kapanidis, Achillefs N. .
NATURE METHODS, 2011, 8 (04) :279-280
[19]   Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy [J].
Huang, Bo ;
Wang, Wenqin ;
Bates, Mark ;
Zhuang, Xiaowei .
SCIENCE, 2008, 319 (5864) :810-813
[20]   Whole-cell 3D STORM reveals interactions between cellular structures with nanometer-scale resolution [J].
Huang, Bo ;
Jones, Sara A. ;
Brandenburg, Boerries ;
Zhuang, Xiaowei .
NATURE METHODS, 2008, 5 (12) :1047-1052