Immunocytochemical Visualization of Proteins from Cyanobacterial Cells with High Autofluorescence of Phycoerythrin and Phycourobilin

0582456 - MBÚ 2024 RIV US eng J - Journal Article
Masuda, Takako - Majerová, Dominika - Piwosz, Kasia - Tsurumaki, Tatsuhiro - Fujita, Y. - Prášil, Ondřej
Immunocytochemical Visualization of Proteins from Cyanobacterial Cells with High Autofluorescence of Phycoerythrin and Phycourobilin.
Jove-Journal of Visualized Experiments. Roč. 2023, č. 199 (2023), č. článku e65168. ISSN 1940-087X
R&D Projects: GA ČR(CZ) GA20-17627S
Grant - others:AV ČR(CZ) JPJSBP 120222502
Institutional support: RVO:61388971
Keywords : Chlorophyl * phycoerythrin * cyanobacterium * phycourobilin
OECD category: Microbiology
Impact factor: 1.2, year: 2022
Method of publishing: Limited access
https://www.jove.com/t/65168/immunocytochemical-visualization-proteins-from-cyanobacterial-cells

Presented is a protocol for visualizing and quantifying a specific protein in cells at the cellular level for the marine cyanobacterium Crocosphaera watsonii, a crucial primary producer and nitrogen fixer in oligotrophic oceans. One of the challenges for marine autotrophic N2 fixers (diazotrophs) is distinguishing probe-derived fluorescence signals from autofluorescence. C. watsonii was selected to represent chlorophyll-, phycoerythrin-and phycourobilin-containing cyanobacteria. The protocol allows for simple and semi-quantitative visualization of proteins in C. watsonii at a single-cell level, enabling investigation of protein production under different environmental conditions to evaluate the metabolic activities of the target cyanobacteria. Furthermore, the fixation and permeabilization methods are optimized to enhance the fluorescence signals from target proteins to distinguish them from autofluorescence, especially from phycoerythrin and phycourobilin. The enhanced signal can be visualized using confocal or widefield fluorescence microscopy. Additionally, fluorescence intensity was semi-quantified using Fiji software. This single-cell analysis workflow allows the evaluation of cell-to-cell variations of specific protein content. The protocol can be performed in any life science laboratory as it requires only standard equipment and can also be easily adapted to other phycoerythrin-containing cyanobacterial cells. © 2023 JoVE Journal of Visualized Experiments.
Permanent Link: https://hdl.handle.net/11104/0350526