Literature DB >> 3116667

The use of a charge-coupled device for quantitative optical microscopy of biological structures.

Y Hiraoka1, J W Sedat, D A Agard.   

Abstract

The properties of a charge-coupled device (CCD) and its application to the high-resolution analysis of biological structures by optical microscopy are described. The CCD, with its high resolution, high sensitivity, wide dynamic range, photometric accuracy, and geometric stability, can provide data of such high quality that quantitative analysis on two- and three-dimensional microscopic images is possible. For example, the three-dimensional imaging properties of an epifluorescence microscope have been quantitatively determined with the CCD. This description of the imaging properties of the microscope, and the high-quality image data provided by the CCD, allow sophisticated computational image processing methods to be used that greatly improve the effective resolution obtainable for biological structures. Image processing techniques revealed fine substructures in Drosophila embryonic diploid chromosomes in two and three dimensions. The same approach can be extended to structures as small as yeast chromosomes or to other problems in structural cell biology.

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Year:  1987        PMID: 3116667     DOI: 10.1126/science.3116667

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  48 in total

1.  Actin protofilament orientation in deformation of the erythrocyte membrane skeleton.

Authors:  C Picart; P Dalhaimer; D E Discher
Journal:  Biophys J       Date:  2000-12       Impact factor: 4.033

2.  Fluorescence lifetime imaging.

Authors:  J R Lakowicz; H Szmacinski; K Nowaczyk; K W Berndt; M Johnson
Journal:  Anal Biochem       Date:  1992-05-01       Impact factor: 3.365

3.  Specific features in linear and spatial organizations of pericentromeric heterochromatin regions in polytene chromosomes of the closely related species Drosophila virilis and D. kanekoi (Diptera: Drosophilidae).

Authors:  Irina Wasserlauf; Konstantin Usov; Gleb Artemov; Tatyana Anan'ina; Vladimir Stegniy
Journal:  Genetica       Date:  2015-02-27       Impact factor: 1.082

4.  Measurement of marine picoplankton cell size by using a cooled, charge-coupled device camera with image-analyzed fluorescence microscopy.

Authors:  C L Viles; M E Sieracki
Journal:  Appl Environ Microbiol       Date:  1992-02       Impact factor: 4.792

5.  Time resolved imaging microscopy. Phosphorescence and delayed fluorescence imaging.

Authors:  G Marriott; R M Clegg; D J Arndt-Jovin; T M Jovin
Journal:  Biophys J       Date:  1991-12       Impact factor: 4.033

6.  Inhibitors of phosphoinositide 3-kinase cause defects in the postendocytic sorting of beta2-adrenergic receptors.

Authors:  Hibah O Awwad; Varsha Iyer; Jennifer L Rosenfeld; Ellen E Millman; Estrella Foster; Robert H Moore; Brian J Knoll
Journal:  Exp Cell Res       Date:  2007-05-22       Impact factor: 3.905

7.  Distribution of the rDNA and three classes of highly repetitive DNA in the chromatin of interphase nuclei of Arabidopsis thaliana.

Authors:  S Bauwens; P Van Oostveldt; G Engler; M Van Montagu
Journal:  Chromosoma       Date:  1991-10       Impact factor: 4.316

8.  Fluorescence lifetime imaging of free and protein-bound NADH.

Authors:  J R Lakowicz; H Szmacinski; K Nowaczyk; M L Johnson
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

9.  High content cell screening in a microfluidic device.

Authors:  Raymond Cheong; Chiaochun Joanne Wang; Andre Levchenko
Journal:  Mol Cell Proteomics       Date:  2008-10-24       Impact factor: 5.911

10.  Impact of New Camera Technologies on Discoveries in Cell Biology.

Authors:  Nico Stuurman; Ronald D Vale
Journal:  Biol Bull       Date:  2016-08       Impact factor: 1.818

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