• Home
• Team
  • Our Team
  • Photo Gallery
  • Collaborations
  • Official team profile
• Project
  • Overview
  • Introduction
  • Golden Gate Standard
  • The TAL Vector
  • GATE Assembly Kit
  • Using the Toolkit
  • The Future of TAL
  • Experiments and Results
• Notebook
  • Labbook Toolkit
  • Labbook TAL Vector
  • Methods
• Parts
• Safety
• Modeling
  • Companel|DNA
  • Download
• Human Practices
  • Overview
  • Philosophical Analysis
  • Educational Outreach
  • Public Outreach
• Attributions
• 

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 experiment and what you want to do, when working with TAL proteins its pretty clear you want to target a dna sequence. To choose your sequence you need to know some of the limitations of TAL proteins to pick it the right way.

1. Every TAL protein starts and ends with a Thymin

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

2. Your sequence must be twelve bases long

Our Toolbox is optimized for sequences of twelve plus two (the thymin at upstream and downstrem) this lenght guarantes a high enough specifity and at the same time a librarysize that good to handle.

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

Step 2. Building a TAL

For building your TAL you start with your selected sequence, in this manual we use a fictive sequence that you can substitute with your own.

Our sequence will be:

Because the two thymins are already in the cloning vector they are not interesting 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 posible pair of bases like for example AA we have 6 places. Every place stands for one of the six possiple positions of the pair AA inside the TAL protein.

All you have to do now is pick the six direpeats consistend with the six pairs of bases 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 that every direpeat knows through his downstream and upstream part at which position of the final TAL protein it belongs. You can find the exact theory behind this in the "Building a toolkit" part in the project section of this wiki.

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.