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This protocol outlines the visualization and quantification of a particular protein within cells at the cellular level for the phycoerythrin-containing cyanobacterium, Crocosphaera watsonii.
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.
The physiological variation from cell to cell (commonly referred to as "heterogeneity") in metabolic activities within microorganisms, including cyanobacteria, has been documented through studies on clone cultures1,2,3,4. This heterogeneity encompasses diverse metabolic activities such as cell division5, carbon assimilation6,7,8, and nitrogen assimilation9,10.....
1. Cyanobacteria cultivation
2. Preparation of reagents<.......
The fluorescence signal was observed from extracellular substances in the negative control, where the 1st antibody was not used (Figure 1A-C). The fluorescence signal of the tyramide-boosted reagent, conjugated to the large subunit of the Rubisco protein (RbcL), was successfully detected in C. watsonii under a fluorescence microscope using a DAPI filter with UV excitation (Figure 1D-F.......
For cyanobacteria, the TSA system has found widespread use in TSA-fluorescence in situ hybridization (TSA-FISH, CARD-FISH), targeting specific rRNA. However, its application for proteins remains limited26. In this study, a TSA procedure was applied to enable whole-cell immunodetection of the N2-fixing cyanobacterium C. watsonii, incorporating modifications based on a previous reference20. Notable revisions encompassed permeabilization, acco.......
We appreciate Dr. Radek Kana and Barbora Šedivá for assistance with confocal microscopic analysis and Dr. Roman Sobotka and Dr. Kateřina Bišová for advice in immunodetection and fluorescence microscopy analysis. This research was financially supported by Czech Research Foundation GAČR (project 20-17627S to OP and TM), the Mobility plus project between JSPS and Czech Academy of Sciences (JPJSBP 120222502), and JSPS KAKENHI (project 23H02301).
....Name | Company | Catalog Number | Comments |
Achromopeptidase | FUJIFILM | 014-09661 | |
Alexa Fluor350 | Thermo Scientific | B40952 | Tyramide-350 |
Alexa Fluor405 | Thermo Scientific | B48254 | Tyramide-405 |
Alexa Fluor488 Tyramide SuperBoost Kit | Thermo Scientific | B40922 | Goat anti-rabbit IgG |
Bovine serum albumin | Sigma-Aldrich | A2153 | |
Centrifuge | Eppendorf | 5804 R | |
Centrifuge tubes (15 mL) | VWR | 525-1085 | For harvesting cells |
Confocal microscope | Zeiss | LSM880 | Equipped with Airyscan |
Fluorescence microscope | Olympus | BX51 | DAPI filter: Ex.360-370 nm, Em. 420-460 nm |
Gelatine | Merk | 4070 | |
High precision microscope cover glasses for confocal microscope | Deckgläser | No. 1.5H | |
Liquid Blocker Regular/Mini | Daido Sangyo Co., Ltd. | Part 6505 | For keeping the cells on the slide glass |
Lysozyme | ITW Reagents | A4972 | |
Methanol | Carl Roth | 67-56-1 | |
Monopotassium Phosphate | Penta | 12290 | |
Monunting medium | Sigma-Aldrich | 345789-20ML | FluorSave Reagent |
Mounting medium | Vectashild | H-1300 | |
Objective lens used in the confocal microscope | Zeiss | Plan-Apochromat 63x/1.4 Oil DIC M27 | |
Paraformaldehyde | Sigma-Aldrich | 158127 | |
Poly-lysine coated slide glass | Sigma-Aldrich | P0425-72EA | |
Potassium chloride | Lach-Ner | ||
Safe lock tube (1.5 mL) | Eppendorf | 0030 120.086 | For treating cells and storing chemicals |
Sodium chloride | Penta | 16610 | |
Sodium hydrogen phosphate | Penta | 15130 | |
Triton X-100 | Sigma-Aldrich | X100 |
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