Team:SJTU-BioX-Shanghai/Modeling

From 2014.igem.org

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<p>We designed fifteen sequences derived from raw sequence. These mutated sequences contain different mutations, ranging from one to five. Through a series of calculations, we obtained scores to represent the binding of TAL effectors and DNA.</p>
<p>We designed fifteen sequences derived from raw sequence. These mutated sequences contain different mutations, ranging from one to five. Through a series of calculations, we obtained scores to represent the binding of TAL effectors and DNA.</p>
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<li><strong>mutation-1</strong><br/><img src="http://2014.igem.org/File:SJTU14_seq15.jpg"></img></li>
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Revision as of 13:43, 16 October 2014

Part I Single Cell


Our project is about the system involving various enzymes, mostly the series enzymes, combining into certain area. This area can be more efficient when it comes to synthesizing or degrading chemicals. So the first question is, whether this system can be so useful when distributing multiple similar areas in a single cell.

   Four Types of Distribution


  • Type 1: Membrane & Random
    The position of enzyme is distributed randomly in the cell membrane.
  • Type 2: Membrane & Polymerization
    The polymerization of certain enzymes, based on MembRing, is distributed randomly inside the cell.
  • Type 3: Matrix & Random
    The position of enzyme is distributed randomly inside the cell.
  • Type 4: Matrix & Random
    The polymerization of certain enzymes, based on MembRing, is distributed randomly inside the cell.

   Hypothesis of Simulation


  1. Metabolism
    [图片一]
    Enzymes: E0, E1,E2
    Substrates:S0,S1,S2,S3
  2. Initial Distribution of Substrates
    All substrates are randomly distributed OUTSIDE the cell in all four simulations.
  3. Movement of Substrates
    The motion of molecules is random, including the rate and orientation.
  4. Catalytic reaction
    The time period of reaction is neglected. When the type of chemical match the type of enzyme, distance is less than threshold, then the enzyme reaction is recognized and recorded.
  5. Other Hypothesis
    Other physical and chemical parameters are under the scaling rule. The whole modeling combined with periodic boundary condition(PBC) to show the real performance of substrates and enzyme system.

   Results:


  • All Results
  • Type 1
  • Type 2
  • Type 3
  • Type 4

Part II Docking

   Why do we need Docking?


    Biobrick designers and users want to understand the characteristics of a particular biobrick, especially the performance and accuracy. Because they need to answer a question, that is, were there to be a certain mutation, whether a huge change would happen to the protein function. We hope to introduce evaluation methods of bioinformatics, to evaluate binding of protein and DNA.

       Materials


      TAL (transcription activator-like) effectors, secreted by phytopathogenic bacteria, recognize host DNA sequences through a central domain of tandem repeats. Each repeat consists of 33 to 35 conserved amino acids and targets a specific base pair by using two hypervariable residues [known as repeat variable diresidues (RVDs)] at positions 12 and 13.

    • PDB:3V6T
    • 【图片1】
    • 【图片2】
    •    Mutations


        We designed fifteen sequences derived from raw sequence. These mutated sequences contain different mutations, ranging from one to five. Through a series of calculations, we obtained scores to represent the binding of TAL effectors and DNA.

      • mutation-1
      • 【图片2】
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      • PDB:3V6T
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      • PDB:3V6T
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      • PDB:3V6T
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      • PDB:3V6T
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      • PDB:3V6T
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      • PDB:3V6T
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      • PDB:3V6T
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