Team:UiOslo Norway/Discussion
Discussion
We experienced that the yeast samples we got did not emit enough light to examine it on a CCD-camera. Our pure sfGFP sample made considerably more light as it had more concentrated solvent of sfGFP to prove lasing. We used this sample to try to make the most ideal setup for the yeast, which we later would try.
Mirrors
One possible reason why the proof of concept did not work was the mirrors. Due to lack of proper equipment with the correct specs at UiO, we improvised by using filters and concave mirrors to achieve the "shortpass dichroic mirrors"-effect. Thanks to Thorlabs that were so kind to sponsor us, we got the mirrors we thought we needed. We made a change in our setup and tried to align the mirrors correctly, but as we were unsuccessful we believe that the alignment was not as perfect as it should have been.Intensity
Another possible reason why the proof of concept did not work might be that our light source did not have high enough intensity. We tried with both adding more diodes and to concentrate the light beam, but neither one of these made us see any trace of lasing with the CCD-camera. We did see some light in our spectrometer, but since it did not show up on the camera, it is difficult to say what kind of properties the light had.sfGFP
Our last possible reason why we were not able to prove the concept of a biolaser is the sample of sfGFP. As we used the same sample for testing for over a moth, we suspected that it began to get old. When we finally felt confident in our setup, we noticed that the sample emitted some red light it had not emitted before. Since this was only a couple of days before the wiki freeze, we did not have time to make a new sample.Notes
It was unfortunate that we were able to see the light from our sample in the spectrometer, but not in the CCD-camera. Even though we aligned everything as it should be and were confident that the setup would be able to send the light into the detector on the camera, we could not see anything. Also, the fact that our sample emitted red light was peculiar, but neither our team mates or our supervisors could come up with a proper reason for why it suddenly changed color, only guesses. Some tips for projects in the future is therefore to study how a proper setup should be and calculate distances and proper alignment in advance. Lastly, we believe it is wise to change the sample used for testing frequently, to avoid weird results.Biological system
The extracted sfGFP had impurities as we can see in the results of SDS-PAGE for the first experiment. Therefore, not all 35.35 mg is sfGFP, but for our purposes, it was good enough. The main goal is to use yeast cells that are expressing sfGFP as a gain medium, and in that case as well there are impurities in the form of subcellular components of yeast cells. Therefore, that should not be a problem for our purposes.We were able to properly clone and submit the composite part, as well as the NMT1-promoter we made, but due to time constraint we were unable to test our system in yeast cells. Because of this, we used an existing expressions system to grow GFP-expressing yeast cells and use that to test our laser. This, combined with the sfGFP-solutions, gave us the material we needed to be able to conduct proper experiments with our setup.
