Measurement of GFP fluorescence is a useful tool for quantifying gene expression. When carrying out this type of work, researchers often wish to state their data as a measurement of fluorescence per cell. Currently, the fluorescence per cell measurement can be variable due to differences between:

units of measurement
data processing settings
device model

To find fluorescence per cell values, typically the measured fluorescence is divided by the OD₆₀₀ as an approximation of a cell number. This can also be imprecise and variable when measured on different devices.

The aim of the Fifth InterLab study is to make fluorescence per cell measurements more compatible among various laboratories around the world by investigating the fluorescence of eight test devices built from BioBrick parts. By standardising the protocol for the plate reader calibration with LUDOX solution, silica beads, and fluorescein, we hope to reduce variability between our results and those of other iGEM teams. OD₆₀₀ values will be associated with colony forming units (CFUs) to achieve a more accurate measurement of fluorescence per cell.

- Protocols -

All InterLab protocols were provided by iGEM

Calibration 1: OD₆₀₀ Reference point - LUDOX Protocol

LUDOX CL-X was used as a single reference point for the plate reader calibration. Using the correction factor obtained from the data, absorbance (Abs600) values from the plate reader were converted into a comparable OD600 measurement and so the variability between path lengths was avoided.

400 μl of the LUDOX solution was added into four separate wells (100 μl each) in the 96-well plate. The same was done with 400 μl of the ddH2O. OD600 measurements were taken and the correction factor of 3.190 was obtained, see the table with results below:

Calibration 2: Particle Standard Curve - Microsphere Protocol

Silica beads - Microsphere suspension was used to construct a standard curve of a particle concentration that was instrumental in estimating the amount of particles/cells from the OD₆₀₀ measurement.

To prepare a Silica beads stock solution, microsphere suspension was vigorously vortexed for 30 seconds and 96 μl was quickly transferred into 1.5 ml eppendorf tube and diluted up to 1 ml with ddH₂O. A set of ten 2-fold serial dilutions in ddH₂O was performed.

The OD₆₀₀ measurements were taken, see the table with results below:

Calibration 3: Fluorescence standard curve - Fluorescein Protocol

The units of fluorescence detected depend on the apparatus used and so to compare results from different teams, a standard curve should be made. To do that, all teams used the same fluorescein molecule to take measurements and construct a curve.

To prepare a 10x fluorescein solution, the tube with fluorescein powder (100 μM dried down) was centrifuged for 30 s at 775 xg and resuspended in 1 ml 1x PBS. Then, 1x fluorescein stock was made by mixing 100 μl of 10x fluorescein solution with 900 μl of 1x PBS. The set of ten 2-fold serial dilutions in 1x PBS was performed.

The fluorescence was measured, see the results below:

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Plates used (Corning Incorporated Costar 3603)

96-well plate, black with clear and flat bottom.

Plate reader (BMG LabTech Clariostar ) settings

OD₆₀₀

All OD600 measurements were taken using the same settings:

27 °C
Path length correction off
35 flashes per well
Double orbital shaking mode with the frequency of 400 rpm for 10s before reading

Fluorescence

All fluorescence measurements were taken using the same settings:

27 °C
Bottom optics
Excitation wavelength 485-15 nm
Emission wavelength 525-15 nm
Well scan with orbital averaging of 3
25 flashes per well
The gain setting 1500
Focal height 4.8
Double orbital shaking mode with the frequency of 500 rpm for 10s before reading

Team:Manchester/InterLab

InterLab Study

- The Fifth InterLab Study -