Introduction

Why?

Hockberger et al (1999) suggest that blue light up to 470 nm can have some phototoxic effect on mammalian cells, from 2 to 6 J/cm². In our experiments, we have observed a much higher cell death rate in the cultures exposed for 24h to blue light than in the control. 24h at 20 mW/m² is actually more than 1700 J/cm². To stay on the safe side, and give the cells 6 J/cm² during 4 hours would mean an average of 0.4 mW/cm².

• How much activation can we get with this rate?
• Will we have to push it up?
• What lighting pattern will give best results?

What?

To optimize the number of experiments to perform, we have built a simple model to predict the proportion of photoproduct to be expected at every time point when a sample with LovTAP-VP16 when it's illuminated with a time varying light input.

How?

Photoactication

When light with the appropriate wavelength goes through a solution with photoactive molecules, a number of photons will be absorbed and transfer their energy to these molecules. In the case of LovTAP-VP16, this energy will favor the conformational change into the “active” state. To simplify the model, we will suppose that the protein will be active once it has received enough energy.

The molar absorptivity, also know as extinction coefficient, ε, is directly related to the absorption cross section, σ, through the formula:

If ε is in L mol⁻¹cm⁻¹ we get σ in m². From it we can calculate the number of photons absorbed by a material per unit of distance traveled by the light, using the expression:

where N is the number of photons, m is the number of absorbing molecules per unit volume and x is distance. We can write m in terms of the amount of molecules in the differential volume dV:

Dagradation

Since the ground state, or dark state, is more stable, active LovTAP-VP16 proteins will spontaneously release a photon and go back to the dark state. This rate is parametrized with the half life of the photoproduct.