Literature DB >> 12932771

Saturated patterned excitation microscopy with two-dimensional excitation patterns.

Rainer Heintzmann1.   

Abstract

The techniques of patterned excitation microscopy (PEM, also referred to in the literature as structured illumination, harmonic excitation light microscopy, or laterally modulated excitation microscopy), has recently been extended to the non-linear regime, permitting a further increase in resolution breaking the Abbe diffraction limit (saturated PEM, saturated patterned excitation microscopy (SPEM)). Fluorescence saturation was suggested as the non-linear effect employed to achieve this aim. Here a two-dimensional extension of the linear and the non-linear patterned excitation technique is introduced and simulations of the expected resolution improvement are presented. The simulations account for photon statistics, a sub-optimal degree of modulation and a high amount of background fluorescence in the sample. The resulting point-spread-functions achieve a full width at half maximum of 215 nm (widefield), 118 nm (linear PEM), and 57 nm (saturated PEM, 9x9 orders). For higher resolution, an increased number of detected photons and of raw data images are required. A potential method for substantially decreasing the required number of raw images in PEM and SPEM is discussed.

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Mesh:

Year:  2003        PMID: 12932771     DOI: 10.1016/s0968-4328(03)00053-2

Source DB:  PubMed          Journal:  Micron        ISSN: 0968-4328            Impact factor:   2.251


  21 in total

1.  The limitations of nonlinear fluorescence effect in super resolution saturated structured illumination microscopy system.

Authors:  Aviram Gur; Zeev Zalevsky; Vicente Micó; Javier García; Dror Fixler
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2.  Trends in fluorescence imaging and related techniques to unravel biological information.

Authors:  Elke Haustein; Petra Schwille
Journal:  HFSP J       Date:  2007-09-17

3.  Enhancement of lateral resolution and optical sectioning capability of two-photon fluorescence microscopy by combining temporal-focusing with structured illumination.

Authors:  Keisuke Isobe; Takanori Takeda; Kyohei Mochizuki; Qiyuan Song; Akira Suda; Fumihiko Kannari; Hiroyuki Kawano; Akiko Kumagai; Atsushi Miyawaki; Katsumi Midorikawa
Journal:  Biomed Opt Express       Date:  2013-10-10       Impact factor: 3.732

4.  Structured illumination microscopy of a living cell.

Authors:  Liisa M Hirvonen; Kai Wicker; Ondrej Mandula; Rainer Heintzmann
Journal:  Eur Biophys J       Date:  2009-06-18       Impact factor: 1.733

Review 5.  Widefield fluorescence microscopy with extended resolution.

Authors:  Andreas Stemmer; Markus Beck; Reto Fiolka
Journal:  Histochem Cell Biol       Date:  2008-09-23       Impact factor: 4.304

6.  Nanoscopy of cell architecture: The actin-membrane interface.

Authors:  Sohail Ahmed
Journal:  Bioarchitecture       Date:  2011-01

7.  Saturated excitation of fluorescent proteins for subdiffraction-limited imaging of living cells in three dimensions.

Authors:  Masahito Yamanaka; Kenta Saito; Nicholas I Smith; Satoshi Kawata; Takeharu Nagai; Katsumasa Fujita
Journal:  Interface Focus       Date:  2013-10-06       Impact factor: 3.906

8.  Cellular imaging of deep organ using two-photon Bessel light-sheet nonlinear structured illumination microscopy.

Authors:  Ming Zhao; Han Zhang; Yu Li; Amit Ashok; Rongguang Liang; Weibin Zhou; Leilei Peng
Journal:  Biomed Opt Express       Date:  2014-03-31       Impact factor: 3.732

9.  Highly photostable, reversibly photoswitchable fluorescent protein with high contrast ratio for live-cell superresolution microscopy.

Authors:  Xi Zhang; Mingshu Zhang; Dong Li; Wenting He; Jianxin Peng; Eric Betzig; Pingyong Xu
Journal:  Proc Natl Acad Sci U S A       Date:  2016-08-25       Impact factor: 11.205

Review 10.  A guide to super-resolution fluorescence microscopy.

Authors:  Lothar Schermelleh; Rainer Heintzmann; Heinrich Leonhardt
Journal:  J Cell Biol       Date:  2010-07-19       Impact factor: 10.539

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