1 / 20

TinkerCell Tutorial: The Bacterial Photography System

TinkerCell Tutorial: The Bacterial Photography System. Thanks and appreciation to Deepak Chandra from U of W, who developed TinkerCell and modified it to teach the bacterial photography system. The system itself was made by the 2006 Univ. Texas iGEM team.

daphne-todd
Download Presentation

TinkerCell Tutorial: The Bacterial Photography System

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. TinkerCell Tutorial: The Bacterial Photography System Thanks and appreciation to Deepak Chandra from U of W, who developed TinkerCell and modified it to teach the bacterial photography system. The system itself was made by the 2006 Univ. Texas iGEM team.

  2. Select “New canvas” from the File menu or use the “New” icon at the left of the top toolbar Start a new canvas

  3. From the “Parts” tab, select and place an “Inducible Promoter”, “RBS”, and “Coding” icon on the canvas. Assemble Reporter

  4. Drag items on the canvas next to one another to align them. Rename the promoter “PompC” and the coding sequence “LacZ”. Align and Name

  5. From the “Molecules” tab, add a transcription factor to the canvas and rename it OmpRp Add a transcription factor

  6. Select OmpRp, then from the “Edit” menu, choose “Add Decorator”. From the “Decorator” tab, select “phosphorylation”. Visual appeal: add a 'P'

  7. From the “Regulation” tab, choose “Regulation”, then click OmpRp and PompC. Choose “Transcriptional Activation” from the pop-up. Regulate transcription

  8. From the “Molecules” tab, place a “Receptor” on the canvas and rename it Cph8. Add light receptor

  9. From the “Regulation” tab, choose “Regulation, then click on Cph8 and OmpRp, then select “Allosteric Inhibition” from the popup menu. Regulate OmpRp with Cph8

  10. From the “Molecules” tab, place an “Enzyme” on the canvas. Name it “BetaGal”. Add the BetaGal protein

  11. From the “Reactions” tab, choose “1 to 1” then click on the lacZ orf and the beta-gal protein, and choose “Protein Production” from the popup menu. Produce BetaGal protein

  12. From the “Molecules” tab, place two “small molecules” on the canvas. Name the first “SGal” and the second “COLOR”. Add the colorful molecule

  13. Double-click on SGal, select the “Initial Values” tab, and change its initial concentration from 1 uM to 15. Supply SGal

  14. From the “Reaction” tab, choose “2 to 1”, then click on BetaGal, SGal, and COLOR. Add the color reaction

  15. From the “Compartments” tab, choose “Cell”. Place and resize it on the canvas to include all components (but leave Cph8 in the membrane). Add a chassis

  16. From the “Molecules” tab, place a small molecule outside the cell and rename it “Light”. Add light

  17. From the “Regulation” tab, choose “Regulation” and click on Light and Cph8 and choose “Activation” from the popup menu. Regulate Cph8 with light

  18. From the “Inputs” tab, choose “Step input” and click on the Light molecule. Turn on the light

  19. Double click on the “step” that’s on the canvas then click the numerical icon. Change “Step_time” to 50. Change the timing

  20. Your circuit should be complete. Now you can start modeling the outputs. Use the “play” arrow to run simulations with different inputs for each element. Start Simulating!

More Related