University of Arizona 2006

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The current name of our project is "Water Color." It is a system that selectively expresses one of three florescence proteins. Each of the three florescence proteins will be expressed in the presence of a unique inducer. Each florescent protein will be controlled by a unique repressed promoter. Thus we will have the expression of three flourescent proteins activated by the presence of there respective inducers.
The current name of our project is "Water Color." It is a system that selectively expresses one of three florescence proteins. Each of the three florescence proteins will be expressed in the presence of a unique inducer. Each florescent protein will be controlled by a unique repressed promoter. Thus we will have the expression of three flourescent proteins activated by the presence of there respective inducers.
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The idea of our project is to have a media with these cells on it so that each cell will be individually activated to shown a certain "color" (in actuallity, express one florescent protein, which may or may not look unique). Thus the media is able to dispaly an image. A further idea, to be implemented later, is to have the ability to "erase" the image. This would be accomplished by repressing all three promoters.
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The idea of our project is to have a media with these cells on it so that each cell will be individually activated to shown a certain "color" (in actuallity, express one florescent protein, which may or may not look unique). Thus the media is able to dispaly an image. The spacial resolution with determine how much it will look like an image. A further idea, to be implemented later (time permitting), is to have the ability to "erase" the image. This would be accomplished by repressing all three promoters. Currently, there are no plans to implement this.
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All the requisite parts have been identified from the registry, and will be built together. (More detail on the specific part numbers and a diagram will be added later)
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All the requisite parts have been identified from the registry, and will have constructed them. Specific part numbers and diagram are shown in the parts construction schedule. A flowchart of the parts construction is located at [[University of Arizona 2006/Parts Schedule|Parts Schedule]]
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A flowchart of the parts construction is completed at [[University of Arizona 2006/Parts Schedule|Parts Schedule]]
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We have completed Phase V of the construction (much to our plesant surprise). This means that we have made the final construct. We are currently in the process of sequencing the plasmid, and visualizing the cells with the plasmid.
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We are currently in Phase III of the construction (much to our plesant surprise). This has not taken too long to reach this far, therefore, we will have time to add improvements to the design.
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==Visualization==
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One hurdle to overcome is how should we visualize the image. We know that two of the flourescent proteins look very similar by the naked eye, even though they produce light of different wavelengths. Ideas that we have to better visualize the image include:
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*Making three plates (each one color) for each image and digitally adding color
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*Use light filters to distinguish the proteins
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*View under a microscope
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==Placing the inducer(s)==
==Placing the inducer(s)==
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Similar to the above idea, a PDMS mold with microfluidic channels is made so that a liquid (a solution of inducer) is able to be selectively placed on the plate of cells.
Similar to the above idea, a PDMS mold with microfluidic channels is made so that a liquid (a solution of inducer) is able to be selectively placed on the plate of cells.
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==Visualization==
 +
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One hurdle to overcome is how should we visualize the image. We know that two of the flourescent proteins look very similar by the naked eye, even though they produce light of different wavelengths. Ideas that we have to better visualize the image include:
 +
 +
*Making three plates (each one color) for each image and digitally adding color
 +
 +
*Use light filters to distinguish the proteins
 +
 +
*View under a microscope with filters
==Characterization==
==Characterization==

Revision as of 21:48, 4 October 2006

University of Arizona 2006

UA06 cellraiserslogo.jpg

Contents

Team

The Cell Raisers

"Splice Guys Finish First"

Member Contact Role
Joan Curry curry@ag.arizona.edu Faculty Advisor
Mark Riley riley@ag.arizona.edu Faculty Advisor
Patrick Hollinger dogmod@email.arizona.edu Lab Lead / Design
Josh Kittleson jkittles@email.arizona.edu Lab work, Design
Tim Spriggs tims@u.arizona.edu Project Manager / Documentation
Tyler Brown tylerb@email.arizona.edu Documentation
Dan Reavis danman1@email.arizona.edu
Kevin MacDow macdow@email.arizona.edu
Brian Heinze heinze@email.arizona.edu

Meetings

Lab Work: As needed, various times, various places

Next Meeting: Mon 7/10 in Shantz 440 at 5:00 pm

Resources

Local Resources

  • [http://igem.engr.arizona.edu/phpBB2/ Team Forum]

Articles and References

Related Projects and Links


Projects

Our project ideas that we considered are located at Project Ideas.

We also maintain a forum for internal team communication. This is available at our [http://igem.engr.arizona.edu/phpBB2/ Team Forum].

The "Water Color" system is the project that we are building. As of now, we will be focusing our attention on building this design. We want to start with a system that is not as complex and that is somewhat straightforward to build. So that way, we can learn while we build. We wish to add complexity later, time and resources permitting, after we have made what is already designed.

Project Details

The current name of our project is "Water Color." It is a system that selectively expresses one of three florescence proteins. Each of the three florescence proteins will be expressed in the presence of a unique inducer. Each florescent protein will be controlled by a unique repressed promoter. Thus we will have the expression of three flourescent proteins activated by the presence of there respective inducers.

The idea of our project is to have a media with these cells on it so that each cell will be individually activated to shown a certain "color" (in actuallity, express one florescent protein, which may or may not look unique). Thus the media is able to dispaly an image. The spacial resolution with determine how much it will look like an image. A further idea, to be implemented later (time permitting), is to have the ability to "erase" the image. This would be accomplished by repressing all three promoters. Currently, there are no plans to implement this.

All the requisite parts have been identified from the registry, and will have constructed them. Specific part numbers and diagram are shown in the parts construction schedule. A flowchart of the parts construction is located at Parts Schedule

We have completed Phase V of the construction (much to our plesant surprise). This means that we have made the final construct. We are currently in the process of sequencing the plasmid, and visualizing the cells with the plasmid.

Placing the inducer(s)

After the challenges of the first aspect of the project are overcome, more mechanical challenges still exist. For example: How to place the inducers?, or What scale should the image be?, or Are any optical techniques needed to fully visualize the image?

Inkjet Printer

The first idea to place the inducers on the media is to use an injet printer. The printer could print solutions of inducers on a thin sheet which can be placed onto the media to put the inducers in contact with the cells. Issues that arrise are:

  • The size of molecules and the aperature of the jet
  • The fluid properties of the solution (e.g. viscosity) should match ink
  • The sheet needs to effectively transfer the solutions to the media without mixing of regions

Rapid Prototyping Mold

Digital images could be parsed into its three separate colors. The area were there is color is then cut into a block (not in actuality, it is RP'ed in one step). The block is then used to cast a PDMS mold that will be used as a stamp to place the inducers on the plate of cells.

PDMS Mold

Similar to the above idea, a PDMS mold with microfluidic channels is made so that a liquid (a solution of inducer) is able to be selectively placed on the plate of cells.

Visualization

One hurdle to overcome is how should we visualize the image. We know that two of the flourescent proteins look very similar by the naked eye, even though they produce light of different wavelengths. Ideas that we have to better visualize the image include:

  • Making three plates (each one color) for each image and digitally adding color
  • Use light filters to distinguish the proteins
  • View under a microscope with filters

Characterization

Sequencing

Selection

Imaging

Last Steps

Issues

Currently we are having issues distinguishing the flourescence. Cells with the plasmid alone show up brighter under a flourescent scope than wild type cells. However, once the cells with our plasmid are grown with the inducer, they are only marginally brighter than the cells that were not grown up in inducer. This poses a problem because it is difficult to distinguish between the "on" and "off" states for a certain flourescence.



Photos

Team Photo:

UA iGEM 2006.JPG

Photo page

Personal tools
Past/present/future years