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Here we give you a short manual on how to use our toolkit to design TAL poteins. We recommend reading through all of the manual first prior to toolkit use.

Step 1. The Experiment

First you need to think about your experimental setup. When working with TAL proteins it's pretty clear you want to target a DNA sequence. To choose your sequence you need to know some of the operational details of TAL proteins in order to pick it the right way.

1. Every TAL protein starts and ends with a thymine

This thymine is already inserted in front of your TAL protein when you use our toolkit but it should also be directly upstream of the first base of your target sequence.

2. Your sequence must be twelve bases long

Our Toolbox is optimized for sequences of twelve plus two (the thymine at upstream and downstream positions) this lenght guarantees a high specifity and a library size that's good to handle at the same time.

If you found a sequence that suits these characteristics you can start building your TAL protein.

Step 2. Building a TAL

Building your TAL starts with your selected sequence. In this manual, we use a fictive sequence that you can substitute with your own.

Our sequence will be as follows:

Because the two thymines are already in the cloning vector, they are of no interest for our TAL protein:

To build this sequence from our toolkit we need to split it up in pairs of two:

Now we need to give our pairs position numbers inside the TAL protein:

Now we can start taking the parts out of the toolkit. A short look at the toolkit shows you that for every possible pair of bases, for example AA, we have 6 places. Every place stands for one of the six possible positions of the pair AA inside the TAL protein.

All you have to do now is pick the six direpeats consistent with the six pairs of your sequence. In our case, we would take the the first one of AA because the first pair of bases in our sequence is AA. Then we take the second one of TG the third of AG and so forth. The idea behind this is that every direpeat knows through his downstream and upstream part at which position of the final TAL protein it ought to be. You can find the exact mechanisms behind this in the "Building a toolkit" part of our project section.

Step 3. Adding a Function

Now that you have your TAL biobricks you a almost ready to start working. But targeting a sequence without doing anything is not really helpfull, you need a fusion protein that does something to your DNA. There are a couple of things you could do with your target sequence and normally you have thought of this before you choose your sequence. With our toolkit you get a transcriptionfactor to turn on or enhance the trancription of a gen, a transcriptionfactor to turn down or off the transcription and several other factors like epigeneticmodificators. Every one of these factors is already insde the final TAL vektor and designed to fit at the 3'-end of your TAL biobricks, so you just have to choose one and put it in your reaction tube to the other biobricks.

With the six TAL biobricks and the fusion enzyme in your reaction tube you now only need the typ two restriction enzyme BsmB1 and a T7 Ligase to put all the parts together.