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A microscope calibration protocol for single- molecule microscopy

A microscope calibration protocol for single- molecule microscopy
A microscope calibration protocol for single- molecule microscopy
Single-molecule microscopy allows for the investigation of the dynamics of individual molecules and the visualization of subcellular structures at high spatial resolution. For single-molecule imaging experiments, and particularly those that entail the acquisition of multicolor data, calibration of the microscope and its optical components therefore needs to be carried out at a high level of accuracy. We propose here a method for calibrating a microscope at the nanometer scale, in the sense of determining optical aberrations as revealed by point source localization errors on the order of nanometers. The method is based on the imaging of a standard sample to detect and evaluate the amount of geometric aberration introduced in the optical light path. To provide support for multicolor imaging, it also includes procedures for evaluating the geometric aberration caused by a dichroic filter and the axial chromatic aberration introduced by an objective lens.
1094-4087
182-207
You, Sungyong
06e1ba5a-2d3a-4267-9bfd-ac5abeff555b
Chao, Jerry
550e20b0-8365-42e3-a6fc-1048eb8c2e47
Cohen, Edward A.K.
df5112ce-f48a-4e1f-b7de-4e7d6fbc7cf8
Ward, E. Sally
b31c0877-8abe-485f-b800-244a9d3cd6cc
Ober, R.J. Ober
31f4d47f-fb49-44f5-8ff6-87fc4aff3d36
You, Sungyong
06e1ba5a-2d3a-4267-9bfd-ac5abeff555b
Chao, Jerry
550e20b0-8365-42e3-a6fc-1048eb8c2e47
Cohen, Edward A.K.
df5112ce-f48a-4e1f-b7de-4e7d6fbc7cf8
Ward, E. Sally
b31c0877-8abe-485f-b800-244a9d3cd6cc
Ober, R.J. Ober
31f4d47f-fb49-44f5-8ff6-87fc4aff3d36

You, Sungyong, Chao, Jerry, Cohen, Edward A.K., Ward, E. Sally and Ober, R.J. Ober (2020) A microscope calibration protocol for single- molecule microscopy. Optics Express, 29 (1), 182-207. (doi:10.1364/OE.408361).

Record type: Article

Abstract

Single-molecule microscopy allows for the investigation of the dynamics of individual molecules and the visualization of subcellular structures at high spatial resolution. For single-molecule imaging experiments, and particularly those that entail the acquisition of multicolor data, calibration of the microscope and its optical components therefore needs to be carried out at a high level of accuracy. We propose here a method for calibrating a microscope at the nanometer scale, in the sense of determining optical aberrations as revealed by point source localization errors on the order of nanometers. The method is based on the imaging of a standard sample to detect and evaluate the amount of geometric aberration introduced in the optical light path. To provide support for multicolor imaging, it also includes procedures for evaluating the geometric aberration caused by a dichroic filter and the axial chromatic aberration introduced by an objective lens.

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Accepted/In Press date: 20 October 2020
e-pub ahead of print date: 22 December 2020

Identifiers

Local EPrints ID: 445716
URI: http://eprints.soton.ac.uk/id/eprint/445716
ISSN: 1094-4087
PURE UUID: 04eec929-e460-4e0e-9a11-2dda3c8abe66
ORCID for E. Sally Ward: ORCID iD orcid.org/0000-0003-3232-7238
ORCID for R.J. Ober Ober: ORCID iD orcid.org/0000-0002-1290-7430

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Date deposited: 06 Jan 2021 17:41
Last modified: 17 Mar 2024 03:53

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Contributors

Author: Sungyong You
Author: Jerry Chao
Author: Edward A.K. Cohen
Author: E. Sally Ward ORCID iD
Author: R.J. Ober Ober ORCID iD

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