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Dual objective fluorescence microscopy for single molecule imaging applications

Dual objective fluorescence microscopy for single molecule imaging applications
Dual objective fluorescence microscopy for single molecule imaging applications

Fluorescence microscopy is an invaluable tool for studying biological processes in cells. In the recent past there has been significant interest in imaging cellular processes at the single molecule level. Single molecule experiments remove ensemble averaging effects and provide information that is typically not accessible through bulk experiments. One of the major requirements in single molecule imaging applications is that a sufficient number of photons be detected from the single molecule. This is not only important for the visual identification of single molecules, but also plays a crucial role in the quantitative analysis of the acquired data. Here, we demonstrate the use of a dual objective imaging configuration for single molecule studies. The configuration uses two opposing objective lenses, where one of the objectives is in an inverted position and the other objective is in an upright position. The use of opposing objective lenses has been previously demonstrated in 4pi confocal microscopy and I5M to achieve high axial resolution when compared to confocal/widefield microscopes. Here we emonstrate that the dual objective imaging configuration provides higher photon collection efficiency when compared to a regular microscope for a given illumination condition. As a result, single molecules can be localized with better accuracy when imaged through opposing objective lenses than when imaged through a regular optical microscope. Analytical tools are introduced to estimate the 2D location of single molecules and to characterize the accuracy with which they can be determined.

Fisher information matrix, Localization accuracy, Multifocal plane microscopy, Single molecule tracking
SPIE
Ram, Sripad
559bd560-3817-4e53-8c7a-2f08e4518412
Prabhat, Prashant
e79cffdb-4de8-42cc-b0f7-6d28f6d3c82e
Ward, E. Sally
b31c0877-8abe-485f-b800-244a9d3cd6cc
Ober, Raimund J.
31f4d47f-fb49-44f5-8ff6-87fc4aff3d36
Ram, Sripad
559bd560-3817-4e53-8c7a-2f08e4518412
Prabhat, Prashant
e79cffdb-4de8-42cc-b0f7-6d28f6d3c82e
Ward, E. Sally
b31c0877-8abe-485f-b800-244a9d3cd6cc
Ober, Raimund J.
31f4d47f-fb49-44f5-8ff6-87fc4aff3d36

Ram, Sripad, Prabhat, Prashant, Ward, E. Sally and Ober, Raimund J. (2009) Dual objective fluorescence microscopy for single molecule imaging applications. In Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XVI. vol. 7184, SPIE.. (doi:10.1117/12.808259).

Record type: Conference or Workshop Item (Paper)

Abstract

Fluorescence microscopy is an invaluable tool for studying biological processes in cells. In the recent past there has been significant interest in imaging cellular processes at the single molecule level. Single molecule experiments remove ensemble averaging effects and provide information that is typically not accessible through bulk experiments. One of the major requirements in single molecule imaging applications is that a sufficient number of photons be detected from the single molecule. This is not only important for the visual identification of single molecules, but also plays a crucial role in the quantitative analysis of the acquired data. Here, we demonstrate the use of a dual objective imaging configuration for single molecule studies. The configuration uses two opposing objective lenses, where one of the objectives is in an inverted position and the other objective is in an upright position. The use of opposing objective lenses has been previously demonstrated in 4pi confocal microscopy and I5M to achieve high axial resolution when compared to confocal/widefield microscopes. Here we emonstrate that the dual objective imaging configuration provides higher photon collection efficiency when compared to a regular microscope for a given illumination condition. As a result, single molecules can be localized with better accuracy when imaged through opposing objective lenses than when imaged through a regular optical microscope. Analytical tools are introduced to estimate the 2D location of single molecules and to characterize the accuracy with which they can be determined.

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More information

Published date: 2009
Venue - Dates: Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XVI, , San Jose, CA, United States, 2009-01-26 - 2009-01-29
Keywords: Fisher information matrix, Localization accuracy, Multifocal plane microscopy, Single molecule tracking

Identifiers

Local EPrints ID: 423608
URI: http://eprints.soton.ac.uk/id/eprint/423608
PURE UUID: b1908ce5-8a35-4311-b773-f96d82ae545a
ORCID for E. Sally Ward: ORCID iD orcid.org/0000-0003-3232-7238
ORCID for Raimund J. Ober: ORCID iD orcid.org/0000-0002-1290-7430

Catalogue record

Date deposited: 27 Sep 2018 16:30
Last modified: 16 Mar 2024 04:37

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Contributors

Author: Sripad Ram
Author: Prashant Prabhat
Author: E. Sally Ward ORCID iD
Author: Raimund J. Ober ORCID iD

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