Literature DB >> 8145084

Artifacts in computational optical-sectioning microscopy.

J G McNally1, C Preza, J A Conchello, L J Thomas.   

Abstract

We tested the most complete optical model available for computational optical-sectioning microscopy and obtained four main results. First, we observed good agreement between experimental and theoretical point-spread functions (PSF's) under a variety of imaging conditions. Second, using these PSF's, we found that a linear restoration method yielded reconstructed images of a well-defined phantom object (a 10-microns-diameter fluorescent bead) that closely resembled the theoretically determined, best-possible linear reconstruction of the object. Third, this best linear reconstruction suffered from a (to our knowledge) previously undescribed artifactual axial elongation whose principal cause was not increased axial blur but rather the conical shape of the null space intrinsic to nonconfocal three-dimensional (3D) microscopy. Fourth, when 10-microns phantom beads were embedded at different depths in a transparent medium, reconstructed bead images were progressively degraded with depth unless they were reconstructed with use of a PSF determined at the bead's depth. We conclude that (1) the optical model for optical sectioning is reasonably accurate; (2) if PSF shift variance cannot be avoided by adjustment of the optics, then reconstruction methods must be modified to account for this effect; and (3) alternative microscopical or nonlinear algorithmic approaches are required for overcoming artifacts imposed by the missing cone of frequencies that is intrinsic to nonconfocal 3D microscopy.

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Year:  1994        PMID: 8145084     DOI: 10.1364/josaa.11.001056

Source DB:  PubMed          Journal:  J Opt Soc Am A Opt Image Sci Vis        ISSN: 1084-7529            Impact factor:   2.129


  5 in total

1.  In vivo observations of myosin II dynamics support a role in rear retraction.

Authors:  P A Clow; J G McNally
Journal:  Mol Biol Cell       Date:  1999-05       Impact factor: 4.138

2.  Covisualization by computational optical-sectioning microscopy of integrin and associated proteins at the cell membrane of living onion protoplasts.

Authors:  J S Gens; C Reuzeau; K W Doolittle; J G McNally; B G Pickard
Journal:  Protoplasma       Date:  1996       Impact factor: 3.356

3.  High-resolution solid modeling of biological samples imaged with 3D fluorescence microscopy.

Authors:  Michael C Ferko; Brian W Patterson; Peter J Butler
Journal:  Microsc Res Tech       Date:  2006-08       Impact factor: 2.769

4.  Realistic 3D coherent transfer function inverse filtering of complex fields.

Authors:  Yann Cotte; Fatih M Toy; Cristian Arfire; Shan Shan Kou; Daniel Boss; Isabelle Bergoënd; Christian Depeursinge
Journal:  Biomed Opt Express       Date:  2011-07-08       Impact factor: 3.732

5.  Assembly and function of the actin cytoskeleton of yeast: relationships between cables and patches.

Authors:  T S Karpova; J G McNally; S L Moltz; J A Cooper
Journal:  J Cell Biol       Date:  1998-09-21       Impact factor: 10.539

  5 in total

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