» Articles » PMID: 35340614

Recent Advances in the Standardization of Fluorescence Microscopy for Quantitative Image Analysis

Overview
Journal Biophys Rev
Publisher Springer
Specialty Biophysics
Date 2022 Mar 28
PMID 35340614
Authors
Affiliations
Soon will be listed here.
Abstract

Fluorescence microscopy is a broadly used technique within a variety of different fields, including life sciences and medical research, and its quantitative aspects are becoming emphasized. The challenge now lies in improving the accuracy and precision of the measurements obtained from fluorescence microscopy. Improving these will facilitate the comparison of results between different instruments/institutions and therefore ensure the reproducibility of results. In this review, recent standardization procedures, including the benchmarking of the instrument performance and the standardization of the image itself, as well as the reference materials for calibration are summarized, and an overview of the advances in fluorescence microscopy standardization and the current limitations are presented. A procedure for the comparison of the image data obtained using different instruments, by different analysts and/or at different times, should be developed to improve the standardization of this data. The standardization of image data would lead to the development of new applications of fluorescence microscopy not only in academic research but also in regulatory science.

Citing Articles

Fluorescence super-resolution microscopy via fluctuation-based multi-route synergy.

Zeng Z, Xu B, Qiu J, Chen X, Huang Y, Xu C Biomed Opt Express. 2024; 15(10):5886-5900.

PMID: 39421781 PMC: 11482186. DOI: 10.1364/BOE.534067.


A NIR-Fluorochrome for Live Cell Dual Emission and Lifetime Tracking from the First Plasma Membrane Interaction to Subcellular and Extracellular Locales.

Booth E, Garre M, Wu D, Daly H, OShea D Molecules. 2024; 29(11).

PMID: 38893352 PMC: 11174088. DOI: 10.3390/molecules29112474.


More than double the fun with two-photon excitation microscopy.

Luu P, Fraser S, Schneider F Commun Biol. 2024; 7(1):364.

PMID: 38531976 PMC: 10966063. DOI: 10.1038/s42003-024-06057-0.


An Image Processing Algorithm for Facile and Reproducible Quantification of Vomocytosis.

Senthil N, Pacifici N, Cruz-Acuna M, Diener A, Han H, Lewis J Chem Biomed Imaging. 2023; 1(9):831-842.

PMID: 38155727 PMC: 10751783. DOI: 10.1021/cbmi.3c00102.


Comparing and Correcting Spectral Sensitivities between Multispectral Microscopes: A Prerequisite to Clinical Implementation.

Eminizer M, Nagy M, Engle E, Soto-Diaz S, Jorquera A, Roskes J Cancers (Basel). 2023; 15(12).

PMID: 37370719 PMC: 10296646. DOI: 10.3390/cancers15123109.


References
1.
Murray J, Appleton P, Swedlow J, Waters J . Evaluating performance in three-dimensional fluorescence microscopy. J Microsc. 2007; 228(Pt 3):390-405. PMC: 2438600. DOI: 10.1111/j.1365-2818.2007.01861.x. View

2.
Leonard A, Cameron R, Speiser J, Wolf B, Peterson Y, Schnellmann R . Quantitative analysis of mitochondrial morphology and membrane potential in living cells using high-content imaging, machine learning, and morphological binning. Biochim Biophys Acta. 2014; 1853(2):348-60. PMC: 4289477. DOI: 10.1016/j.bbamcr.2014.11.002. View

3.
Montero Llopis P, Senft R, Ross-Elliott T, Stephansky R, Keeley D, Koshar P . Best practices and tools for reporting reproducible fluorescence microscopy methods. Nat Methods. 2021; 18(12):1463-1476. DOI: 10.1038/s41592-021-01156-w. View

4.
Petersen N, Hoddelius P, Wiseman P, Seger O, Magnusson K . Quantitation of membrane receptor distributions by image correlation spectroscopy: concept and application. Biophys J. 1993; 65(3):1135-46. PMC: 1225831. DOI: 10.1016/S0006-3495(93)81173-1. View

5.
Wang K, Wu C, Shimajiri S, Enomoto T, Kubota H, Akiyama H . Quantitative immunohistochemistry using an antibody-fused bioluminescent protein. Biotechniques. 2020; 69(4):302-306. DOI: 10.2144/btn-2020-0006. View