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 Na₂HPO₄ (50 mM, pH 9.2)

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

Wash 2 x in Na₂HPO₄ (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 ml cells (2 x 10⁶ with 12 ml 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 ml 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 ml cells and 12 μl unlabeled yeast in 1 ml PB + Trypan blue.

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

Standard curve:

0,2,5,10 μl labeled yeast in 1 ml PB.