Difference between revisions of "Team:Cooper Union/DeNovoSynthesis"

Line 53: Line 53:
 
<h2> Project Description </h2>
 
<h2> Project Description </h2>
  
−
<p>Tell us about your project, describe what moves you and why this is something important for your team.</p>
+
<p>The biology component of our project focused on two main concepts crucial to the functioning of the complete device.  The first of these was to test the idea of bonding DNA to a glass microscope slide as a means of preventing it from being lost in wash steps.  We also sought to characterize different variants of Terminal deoxynucleotidyltransferase (TdT) to find one best suited for the synthesizer.  A third but less pursued topic of study was the possibility of making a heat stable TdT variant using an intein system to circularize the enzyme.</p>
 +
We considered a number of chemical means by which one can bind DNA to glass [1].  The system we chose involved bonding DNA with a five prime thiol modified group to a silanized glass slide.  This method was chosen because the silanization process could be carried out in-house and adding a modified thiol group to the five prime end of DNA is a relatively inexpensive modification.  The methodology was based on a paper by Rogers et al. at Johns Hopkins [2].  After the reaction is complete, the DNA should be bonded to the glass by a disulfide bond.  To test that our glass slides had DNA on them, we would use ethidium bromide since it is known to attach to DNA strands.</p>
 +
In parallel with the glass slides, our team designed three mutated TdT sequences based on a paper by Repasky et al.[3]  In order to characterize these forms of TdT, we would have to ligate them into a high copy expression vector and then transform them into a cell line optimized for expression.  Protein purification of these cells would then follow.  Finally, we would have to test this protein by treating oligonucleotides with the TdT and running them on a polyacrylamide gel.  This would reveal whether or not the TdT can add base pairs to the free three prime end of a DNA molecule.</p>
 +
The intein based TdT system was the lowest on our priority list.  This is because it is only useful if the synthesizer utilizes heat-labile nucleotides.  Ideally, the final system will utilize U.V.-labile nucleotides which would make this system superfluous.  Despite this, we still worked on this angle of the project since U.V.-labile nucleotides are expensive.  In order to circularize TdT, we would have to design a linker sequence between the N and C termini of the protein.  This linker would be incorporated into the TdT sequence along with the intein system.  The remaining steps would be the same as those for our other TdT mutants the only difference being a heating step to insure that the enzyme is heat stable.  </p>
 +
 
 +
<h3>References</h3>
 +
<p>1. Strategies for Attaching Oligonucleotides to Solid Supports. Integrated DNA Technologies (2014).</p>
 +
2. Rogers et al. Immobilization of Oligonucleotides onto a Glass Support via Disulfide Bonds: A Method for Preparation of DNA Microarrays. Analytical Biochemistry 266, 23–30 (1999).</p>
 +
3. Repasky et al. Mutational Analysis of Terminal Deoxynucleotidyltransferase Mediated N-Nucleotide Addition in V(D)J Recombination. Journal of Immunology 172(9):5478-88 (May 2004).</p>
 +
 
 +
 
 
<br />
 
<br />
  

Revision as of 01:52, 18 September 2015

Cooper Union 2015 iGEM



Project Description

The biology component of our project focused on two main concepts crucial to the functioning of the complete device. The first of these was to test the idea of bonding DNA to a glass microscope slide as a means of preventing it from being lost in wash steps. We also sought to characterize different variants of Terminal deoxynucleotidyltransferase (TdT) to find one best suited for the synthesizer. A third but less pursued topic of study was the possibility of making a heat stable TdT variant using an intein system to circularize the enzyme.

We considered a number of chemical means by which one can bind DNA to glass [1]. The system we chose involved bonding DNA with a five prime thiol modified group to a silanized glass slide. This method was chosen because the silanization process could be carried out in-house and adding a modified thiol group to the five prime end of DNA is a relatively inexpensive modification. The methodology was based on a paper by Rogers et al. at Johns Hopkins [2]. After the reaction is complete, the DNA should be bonded to the glass by a disulfide bond. To test that our glass slides had DNA on them, we would use ethidium bromide since it is known to attach to DNA strands.

In parallel with the glass slides, our team designed three mutated TdT sequences based on a paper by Repasky et al.[3] In order to characterize these forms of TdT, we would have to ligate them into a high copy expression vector and then transform them into a cell line optimized for expression. Protein purification of these cells would then follow. Finally, we would have to test this protein by treating oligonucleotides with the TdT and running them on a polyacrylamide gel. This would reveal whether or not the TdT can add base pairs to the free three prime end of a DNA molecule.

The intein based TdT system was the lowest on our priority list. This is because it is only useful if the synthesizer utilizes heat-labile nucleotides. Ideally, the final system will utilize U.V.-labile nucleotides which would make this system superfluous. Despite this, we still worked on this angle of the project since U.V.-labile nucleotides are expensive. In order to circularize TdT, we would have to design a linker sequence between the N and C termini of the protein. This linker would be incorporated into the TdT sequence along with the intein system. The remaining steps would be the same as those for our other TdT mutants the only difference being a heating step to insure that the enzyme is heat stable.

References

1. Strategies for Attaching Oligonucleotides to Solid Supports. Integrated DNA Technologies (2014).

2. Rogers et al. Immobilization of Oligonucleotides onto a Glass Support via Disulfide Bonds: A Method for Preparation of DNA Microarrays. Analytical Biochemistry 266, 23–30 (1999).

3. Repasky et al. Mutational Analysis of Terminal Deoxynucleotidyltransferase Mediated N-Nucleotide Addition in V(D)J Recombination. Journal of Immunology 172(9):5478-88 (May 2004).


What should this page contain?
  • A clear and concise description of your project.
  • A detailed explanation of why your team chose to work on this particular project.
  • References and sources to document your research.
  • Use illustrations and other visual resources to explain your project.

Advice on writing your Project Description

We encourage you to put up a lot of information and content on your wiki, but we also encourage you to include summaries as much as possible. If you think of the sections in your project description as the sections in a publication, you should try to be consist, accurate and unambiguous in your achievements.

Judges like to read your wiki and know exactly what you have achieved. This is how you should think about these sections; from the point of view of the judge evaluating you at the end of the year.


References

iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you though about your project and what works inspired you.

Inspiration

See how other teams have described and presented their projects: