Gérald Grégori, Ph.D Purdue University Cytometry Laboratories

Hansen Life Sciences Research Building, B050201 S. University Street,

West Lafayette, IN 47907-2064,USAPh: +1(765) 494-0757Fax: +1(765) 494-0517

e-mail: gregori@flowcyt.cyto.purdue.edu

Quality Controls: Quality Controls:

Get your instruments Get your instruments under control! under control!

In flow cytometry scatter and fluorescence scales are in arbitrary units

Scatter and Fluorescence values = function of set up (Voltage and gain of PMT)

- +FS-PMT Voltage or gain

Example : beads 10 m

Gre

en F

luor

esce

nce

(au)

Forward Scatter (au)Forward Scatter (au)

Arbitrary units?

Confidence in the instrument performance&

Confidence in the results

Use of a Standard

Quality Control Tests

Daily basis

In theory : • A standard = a reference (defined by a user, a laboratory, or any aknowledged authority)

• Properties accurately known (i.e., provided by the manufacturer)

In practice : • A manufactured particle (fluorescent beads: several sizes and excitation or emission wavelengths)

• A biological particle (i.e., chicken and trout erythrocytes DNA measurements)

• Used as an absolute reference for qualitative and quantitative comparisons

What’s a Standard?

• Check the alignment of the optical pathway

• Check the stability of the machine (Quality Control)

• Test the capacities of the cytometer (flow rate)

• Set up the Sorting (define the delay)

Quality Control of Instruments

0 200 400 600 800 1000FL1 Lin

020

040

060

080

010

00N

umbe

r

1.931.93

0 200 400 600 800 1000FL2 Lin

020

040

060

080

010

0012

0014

00N

umbe

r

1.991.99

0 200 400 600 800 1000FS Lin

020

040

060

080

010

0012

00N

umbe

r 1.371.37CVs < 2% expected for

beads (1-10 μm)

If CVs > 2% check the alignment (flow cell or laser position,

dichroic mirrors)

Very useful on sorters

Beads

Parameter intensity (au)

Num

ber

of e

vent

sTo check the alignment

of the cytometer

Intensity is constant with

time

Example of bad alignment

CV=4.5

0 200 400 600 800 1000FL3 Lin

02

00

40

06

00

80

01

00

01

20

0N

um

be

r 1.62

R4

0 200 400 600 800 1000FL1 Lin

02

00

40

06

00

80

01

00

0N

um

be

r

1.93R2

0 200 400 600 800 1000FL2 Lin

02

00

40

06

00

80

01

00

01

20

01

40

0N

um

be

r

1.99

R3

0 200 400 600 800 1000FS Lin

02

00

40

06

00

80

01

00

01

20

0N

um

be

r 1.37R1

Once a protocol is defined for a particular standard bead solution

Beads must always be plotted in the same regions

Daily quality control

Parameter intensity (au)

Num

ber

of e

vent

s

Internal quality control

Check the stability of the cytometer over time

Many possible problems :

• Leak in the fluidics modified flow rates; instability

• Check for bubbles

• Dirty flow cell

• Laser dying beam intensity decreases

• Bead solution too old or damaged photobleaching

Problem of stability of the cytometer?

For example : Determination of the “dead time” of a Cytoron Absolute (Ortho Diagnostic Systems) Value furnished by the manufacturer = 2000 events s-1

Dilution factor

1

10

100

1000

10000

1 10 100 1000

Measured concentration(beads mm-3)

Sample flow rate = 1mm3 s-1

Test the capacities of the cytometer

Analysis of 1 μm fluorescent bead solutions (dilutions in cascade)

laser

Interrogation point

Flowcell

Last attached undulation

Delay(s)

Piezoelectric Transducer Input

Break-off pointFirst droplet

Electric pulse

++

++

+

++

++

+

Delay determined using

fluorescent beads

Droplet formation and timing

Sort 50 beads on a slide with different delays (ex : from 29 to 35)

•If you achieve 50 out of 50 beads, set the delay to that setting (ex: 31).•If beads are split between 2 drops, adjust the flow cell vertically

3332313029

SlideDrop

Sorting process on the Altra (Coulter, USA)

Green Fluorescence (au)

For

war

d S

catt

er (

au)

beads

Beads (10 m)

Delay value

Count beads(epifluorescent

Microscope)

Set up the delay with fluorescent beads

The necessary step to convert arbitrary units into absolute physical values

Calibration

Calibration = adjustment of an instrument in order to express the results in some accurate physical measure.

Calibrator = a material known to have accurate measured values for one or several characteristics

Example :Quantitation of antibody binding

capacity of cell populations by flow cytometry

Quantum Simply Cellular (QSC)

Identical microbeads with various calibrated binding capacities of goat-anti-mouse IgG on their surface :

Eve

nts

Mean fluorescence intensity (au)

1 2

3 4

Blank

QSC, Cat. No. 815Bangs Laboratories, Inc.www.bangslabs.com

Antibody binding capacity (ABC) provided by the manufacturer :

Blank. 0 MESF

1. 6851 MESF

2. 23379 MESF

3. 58333 MESF

4. 213369 MESF

bead

Ab site

MESF=Molecules of equivalent soluble fluorochrome

QSC Beads (Quantum Simply Cellular)

y = 32790x - 3926.1

R2 = 0.9981

0

50000

100000

150000

200000

250000

0 1 2 3 4 5 6 7

mean fluorescence- HLA-DR-FITC (au)

Mol

ecu

les

of e

qu

ival

ent

solu

ble

fl

uor

och

rom

e (M

ES

F)

Courtesy of K. Rhageb

measure by FCM

corresponding MESF

Binding capacity of cells in your sample

Quantum Simply Cellular Beads Calibration Curve

Absolute Counts Determination of cell concentration

by flow cytometry

Get the control of the volume analyzed

Four different methods

Sample

Cell concentration(# of events / volume)

CYTORON ABSOLUTE(Ortho Diagnostic Systems)

I. Direct Absolute Count

To analyze a bead solution of known concentration Control of the fluidic

Sample

Weigh the sample before analysis

(Weight W0)

Weigh the sample afteranalysis (Weight W1)

Analysis(Flow Cytometer)

Volume analyzed V = (W0 – W1)/

Cell concentration = N/V

cell number (N)

density

DisadvantagesDisadvantages• Time consuming• Less accurate (back flow of sheath fluid in the sample)• Analysis in one run

II. Weigh a Sample

Bead solution (known concentration)•count by microscopy•TruCountTM beads (BD)

Sample

Add a very accurate volume

calculate the bead concentration in the sample (1-10% of the

expected density of the target cells)

Flow Cytometer

cell number (N)

bead numberVolume

analyzed (V)

Cell concentration = N/V

Stewart & Steinkamp, 1982, Cytometry 2 : 238-243

III. Add Beads in the Sample

Hypothesis: flow rate (µl/s) through a flow cytometer = constantBergeron et al, 2003, Cytometry 52B:37-39

Conclusion: volume (V) analyzed in a fixed time = constantNo need to add beads in the samples.

If N events are analyzed by the cytometer in the fixed time

then cell concentration = N/V (cells/µl)

Hint!• Analyzes must be done with the same flow rate

• Volume accurately determined (microscopy, TruCountTM beads) and controlled

• Beads not necessary in the sample, but can be used as internal standard

IV. Determination of the Flow Rate

Quality Control Tests are mandatory … To assess the alignment To assess and control instrument performance

for quantitative and reproducible applications on any flow cytometer.

ReferencesReferencesR.A. Hoffman, Current Protocols in Cytometry, 1997 : 1.3.1-1.3.19J.C.S. Wood, Current Protocols in Cytometry, 1997 : 1.4.1-1.4.12Cytometry, Volume 33, Number 2, 1998 :

Conclusion