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Team:KULeuven/Lab/Key/Lock/AntiKey
From 2009.igem.org
Contents |
Key/Lock/AntiKey
Goal
We want to test the affinity of the key for the lock, and measure the amount of input signals needed to activate transcription. On the other hand we want to test the effect of adding the antikey on the level of transcription.
required
- biobricks:
For the Key device
- J23066 + B0015: De Key sequence with terminator is ordered at GeneArt. - J23110: promotor, plasmid present in the lab. - Restriction enzymes EcoRI, XbaI and SpeI - K12 E. Coli strains ( No special needs)
For the Lock device - J23110: promotor, plasmid present in the lab - J23078: Lock Sequence is ordered at GeneArt - K145015 + B0015: GFP + LVA part present in the lab with terminator attached
For the AntiKey device - K145201: TetR promotor, present in the lab - K238005 + B0015: ordered at GeneArt
Steps
• First all plasmids still present in the lab need to be isolated, so they’re ready to use. Then the GeneArt sequence of the Key can be ligated in the J23110 promotor plasmid.
• Next the J23110 Promotor can be ligated to the GeneArt Lock sequence. If that’s done, the K145015+B0015 construct can be ligated to the promotor/lock sequence.
• These constructed plasmids can then be electroporated into the K12 E. coli cells and a GFP assay can be done, checking if the Key/Lock system works properly. At this time, we also need to measure the intensity or rate of fluorescence, in order to later check if the Antikey works.
• At the same time the K145201 promotor can be ligated to the AntiKey GeneArt sequence, making the Antikey device.
• In order to test the Antikey, all 3 plasmids need to be electroporated into the E.coli strains. Important is that all 3 plasmids contain a different control system (LacZ, Ampicillin or Kanamycin), so we can be sure the strains contain all three plasmids.
• By comparing the GFP results with and without Antikey, we can investigate whether our Antikey has an effect on the transcription of GFP.
Important
I. Always make sure you never cut with an illegal restriction enzyme. II. Make sure the plates you grow the bacteria on contain the right antibiotic. III. You should always be able to identify not only the transformed colonies, but more importantly the recombinant colonies.
