Literature DB >> 19219190

Limits for reduction of effective focal volume in multiple-beam light microscopy.

Anton Arkhipov1, Klaus Schulten.   

Abstract

Employing interference patterns for illumination has been shown to reduce the focal volume in fluorescence microscopy. For example, the 4Pi technique employs two interfering laser beams and significantly decreases the focal volume, as compared to conventional microscopy. We study theoretically the effect of using multiple interfering laser beams on the focal volume. In realistic setups with three or four beams, the focal volume is about half of that from the 4Pi case. This improvement reaches a limit quickly as more beams are added, and for the idealized case of an infinite number of beams the focal volume is rather close to the three- or four-beam cases. Thus, our study suggests a limit for the possible reduction of the focal volume in a purely optical far-field setup.

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Year:  2009        PMID: 19219190      PMCID: PMC3160275          DOI: 10.1364/oe.17.002861

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


  11 in total

1.  Multiple imaging axis microscopy improves resolution for thick-sample applications.

Authors:  Jim Swoger; Jan Huisken; Ernst H K Stelzer
Journal:  Opt Lett       Date:  2003-09-15       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.  Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

Authors:  Michael J Rust; Mark Bates; Xiaowei Zhuang
Journal:  Nat Methods       Date:  2006-08-09       Impact factor: 28.547

4.  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

5.  Ultra-high resolution imaging by fluorescence photoactivation localization microscopy.

Authors:  Samuel T Hess; Thanu P K Girirajan; Michael D Mason
Journal:  Biophys J       Date:  2006-09-15       Impact factor: 4.033

6.  Multiple-objective microscopy with three-dimensional resolution near 100 nm and a long working distance.

Authors:  O Haeberlé; C Xu; A Dieterlen; S Jacquey
Journal:  Opt Lett       Date:  2001-11-01       Impact factor: 3.776

Review 7.  Far-field optical nanoscopy.

Authors:  Stefan W Hell
Journal:  Science       Date:  2007-05-25       Impact factor: 47.728

8.  Excitation strategies for optical lattice microscopy.

Authors:  Eric Betzig
Journal:  Opt Express       Date:  2005-04-18       Impact factor: 3.894

9.  Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy.

Authors:  S W Hell; J Wichmann
Journal:  Opt Lett       Date:  1994-06-01       Impact factor: 3.776

10.  VMD: visual molecular dynamics.

Authors:  W Humphrey; A Dalke; K Schulten
Journal:  J Mol Graph       Date:  1996-02
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