Phagocytosis

Phagocytosis

 

 

Fluorescent labeling of yeast

Resuspend 5 grams of yeast in 50 ml PBS in 100 ml flask

 

 

Put flask for 30 minutes in boiling water bath while stirring.

 

 

Wash 5 x with PBS and 2 x in PB.

 

 

Adjust the concentration to of particles to 10⁹ particles/ml. Can now be frozen at -20 ° C.

 

 

For labeling, resuspend the pellet of 2 x 10¹⁰ particles in 20 ml Na₂ HPO₄ (50 mM, pH 9.2)

 

 

Add 2 mg TRITC, incubate 30 minutes at 37 ° C on a rotary shaker.

 

 

 Wash 2 x in Na₂ HPO₄ (50 mM, pH 9.2) and 4 x in PB.

 

 

Freeze aliquots of 10⁹ particles/ml at -20 ° C.

 

Phagocytosis assay

 

 

Grow cells for at least 5 generation times in HL5, the density not exceeding 5 x 10⁶ cells/ml

 

 

 Harvest 2 x 10⁷ cells, wash 1 x in PB and resuspend in 1 ml PB.

 

 

 Mix 100 m l cells (2 x 10⁶ with 12 m l labelled yeast 1.2 x 10⁷ ) in glass tubes.

 

 

 Incubate for 0, 5, 10, 20, 30 minutes.

 

 

 Stop with 1 ml cold PB.

 

 

 Add 100 m l  Trypan blue (2 mg/ml in 20 mM citrate, 150 mM NaCl, pH 4.5).

 

 

 Mix and shake for 5 minutes.

 

 

 Spin 3 minutes 500 x g.

 

 

 Remove supernatant. Resuspend in 1 ml PB.

 

 

 Read in fluorescence spectrofotometer at 544 nm excitation, 574 nm emission.

 

 

 Include the following blanks:

 

 

 For autofluorescence: 100 m l cells and 12 μl unlabeled yeast in 1 ml PB + Trypan blue.

 

 

 For background, unquenched fluorescence, 12 μ l labeled yeast in 1 ml PB + Trypan blue.

 

 

 Standard curve:

 

 

 0,2,5,10 μ l labeled yeast in 1 ml PB.