Literature DB >> 1738047

Experimental test of an analytical model of aberration in an oil-immersion objective lens used in three-dimensional light microscopy.

S F Gibson1, F Lanni.   

Abstract

Oil-immersion microscope objective lenses have been designed and optimized for the study of thin, two-dimensional object sections that are mounted immediately below the coverslip in a medium that is index matched to the immersion oil. It has been demonstrated both experimentally and through geometrical- and physical-optics theory that, when the microscope is not used with the correct coverslip or immersion oil, when the detector is not located at the optimal plane in image space, or when the object does not satisfy specific conditions, aberration will degrade both the contrast and the resolution of the image. In biology the most severe aberration is introduced when an oil-immersion objective lens is used to study thick specimens, such as living cells and tissues, whose refractive indices are significantly different from that of the immersion oil. We present a model of the three-dimensional imaging properties of a fluorescence light microscope subject to such aberration and compare the imaging properties predicted by the model with those measured experimentally. The model can be used to understand and compensate for aberration introduced to a microscope system under nondesign optical conditions so that both confocal laser scanning microscopy and optical serial sectioning microscopy can be optimized.

Mesh:

Year:  1992        PMID: 1738047     DOI: 10.1364/josaa.9.000154

Source DB:  PubMed          Journal:  J Opt Soc Am A        ISSN: 0740-3232            Impact factor:   2.129


  69 in total

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Journal:  Biophys J       Date:  2003-12       Impact factor: 4.033

2.  Three-dimensional tracking of single secretory granules in live PC12 cells.

Authors:  Dongdong Li; Jun Xiong; Anlian Qu; Tao Xu
Journal:  Biophys J       Date:  2004-09       Impact factor: 4.033

3.  Characterization and adaptive optical correction of aberrations during in vivo imaging in the mouse cortex.

Authors:  Na Ji; Takashi R Sato; Eric Betzig
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-21       Impact factor: 11.205

4.  Measuring and interpreting point spread functions to determine confocal microscope resolution and ensure quality control.

Authors:  Richard W Cole; Tushare Jinadasa; Claire M Brown
Journal:  Nat Protoc       Date:  2011-11-10       Impact factor: 13.491

5.  FluoroSim: A Visual Problem-Solving Environment for Fluorescence Microscopy.

Authors:  Cory W Quammen; Alvin C Richardson; Julian Haase; Benjamin D Harrison; Russell M Taylor; Kerry S Bloom
Journal:  Eurographics Workshop Vis Comput Biomed       Date:  2008-01-01

6.  How accurately can a single molecule be localized in three dimensions using a fluorescence microscope?

Authors:  Sripad Ram; E Sally Ward; Raimund J Ober
Journal:  Proc SPIE Int Soc Opt Eng       Date:  2005

7.  New results on the single molecule localization problem in two and three dimensions.

Authors:  Amir Tahmasb; E Sally Ward; Raimund J Ober
Journal:  Proc SPIE Int Soc Opt Eng       Date:  2015-08-09

8.  Image restoration for three-dimensional fluorescence microscopy using an orthonormal basis for efficient representation of depth-variant point-spread functions.

Authors:  Nurmohammed Patwary; Chrysanthe Preza
Journal:  Biomed Opt Express       Date:  2015-09-08       Impact factor: 3.732

9.  Imaging nanometre-scale structure in cells using in situ aberration correction.

Authors:  C J Fuller; A F Straight
Journal:  J Microsc       Date:  2012-08-20       Impact factor: 1.758

10.  Three-Dimensional Single-Molecule Localization Microscopy in Whole-Cell and Tissue Specimens.

Authors:  Sheng Liu; Hyun Huh; Sang-Hyuk Lee; Fang Huang
Journal:  Annu Rev Biomed Eng       Date:  2020-04-03       Impact factor: 9.590

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