Literature DB >> 32121925

Contrast gain through simple illumination control for wide-field fluorescence imaging of scattering samples.

Zongyue Cheng, Shiyi Sun, Wenbiao Gan, Meng Cui.   

Abstract

Wide field fluorescence microscopy is the most commonly employed fluorescence imaging modality. However, a major drawback of wide field imaging is the very limited imaging depth in scattering samples. By experimentally varying the control of illumination, we found that the optimized illumination profile can lead to large contrast improvement for imaging at a depth beyond four scattering path lengths. At such imaging depth, we found that the achieved image signal-to-noise ratio can rival that of confocal measurement. As the employed illumination control is very simple, the method can be broadly applied to a wide variety of wide field fluorescence imaging systems.

Year:  2020        PMID: 32121925      PMCID: PMC7053499          DOI: 10.1364/OE.385319

Source DB:  PubMed          Journal:  Opt Express        ISSN: 1094-4087            Impact factor:   3.894


  31 in total

1.  Two-photon imaging to a depth of 1000 microm in living brains by use of a Ti:Al2O3 regenerative amplifier.

Authors:  Patrick Theer; Mazahir T Hasan; Winfried Denk
Journal:  Opt Lett       Date:  2003-06-15       Impact factor: 3.776

2.  Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution.

Authors:  Mats G L Gustafsson
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-02       Impact factor: 11.205

3.  Imaging intracellular fluorescent proteins at nanometer resolution.

Authors:  Eric Betzig; George H Patterson; Rachid Sougrat; O Wolf Lindwasser; Scott Olenych; Juan S Bonifacino; Michael W Davidson; Jennifer Lippincott-Schwartz; Harald F Hess
Journal:  Science       Date:  2006-08-10       Impact factor: 47.728

4.  Fast three-dimensional fluorescence imaging of activity in neural populations by objective-coupled planar illumination microscopy.

Authors:  Terrence F Holekamp; Diwakar Turaga; Timothy E Holy
Journal:  Neuron       Date:  2008-03-13       Impact factor: 17.173

5.  Optically sectioned imaging by oblique plane microscopy.

Authors:  C Dunsby
Journal:  Opt Express       Date:  2008-12-08       Impact factor: 3.894

6.  Reconstruction of zebrafish early embryonic development by scanned light sheet microscopy.

Authors:  Philipp J Keller; Annette D Schmidt; Joachim Wittbrodt; Ernst H K Stelzer
Journal:  Science       Date:  2008-10-09       Impact factor: 47.728

7.  Fluctuations and stimulus-induced changes in blood flow observed in individual capillaries in layers 2 through 4 of rat neocortex.

Authors:  D Kleinfeld; P P Mitra; F Helmchen; W Denk
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

8.  On/off blinking and switching behaviour of single molecules of green fluorescent protein.

Authors:  R M Dickson; A B Cubitt; R Y Tsien; W E Moerner
Journal:  Nature       Date:  1997-07-24       Impact factor: 49.962

Review 9.  Fluorescence microscopy in three dimensions.

Authors:  D A Agard; Y Hiraoka; P Shaw; J W Sedat
Journal:  Methods Cell Biol       Date:  1989       Impact factor: 1.441

10.  Lattice light-sheet microscopy: imaging molecules to embryos at high spatiotemporal resolution.

Authors:  Bi-Chang Chen; Wesley R Legant; Kai Wang; Lin Shao; Daniel E Milkie; Michael W Davidson; Chris Janetopoulos; Xufeng S Wu; John A Hammer; Zhe Liu; Brian P English; Yuko Mimori-Kiyosue; Daniel P Romero; Alex T Ritter; Jennifer Lippincott-Schwartz; Lillian Fritz-Laylin; R Dyche Mullins; Diana M Mitchell; Joshua N Bembenek; Anne-Cecile Reymann; Ralph Böhme; Stephan W Grill; Jennifer T Wang; Geraldine Seydoux; U Serdar Tulu; Daniel P Kiehart; Eric Betzig
Journal:  Science       Date:  2014-10-23       Impact factor: 47.728

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