ETH Zurich 2006
From 2006.igem.org
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that the "thing" project sounds much more appropriate for this kind of competition. This would be | that the "thing" project sounds much more appropriate for this kind of competition. This would be | ||
in the end the criteria that would push my vote into this project (after a deeper analysis of the | in the end the criteria that would push my vote into this project (after a deeper analysis of the | ||
- | feasibility and availability of the needed activators and repressors). If we decide to | + | feasibility and availability of the needed activators and repressors).If we decide to go for this |
- | go for this project we can of course reduce the risk factor by taking | + | project we can of course reduce the risk factor by taking different activator - repressor candidates |
- | + | and maybe trying 2 or 3 combinations that have passed through the modelization test. | |
- | that have passed through the modelization test. | + | |
'''Christophe:''' | '''Christophe:''' |
Revision as of 17:30, 14 August 2005
Contents |
Introduction
People
Students
Simon Barkow | Christophe Dessimoz | Zlatko Franjcic |
Dominic Frutiger | Robin Künzler | Urs A. Müller |
Jonas Nart | Kristian Nolde | Alexander Roth |
Tamara Ulrich | Giorgia Valsesia | Herve Vanderschuren |
Supervisors
Jörg Stelling | Sven Panke | Eckart Zitzler |
Advisors
Uwe Sauer | Martin Fussenegger | Andreas Hierlemann |
Kay-Uwe Kirstein | Ruedi Aebersold |
Events & Timeline
Project Ideas
This is the brainstorming section. In this section you will find random ideas and comments without too much consideration of feasability etc. Crazy ideas and wild dreams are welcome!
Individual Phenomena
Designing and tweaking so that the individual behaves in a desired way.
Oscillator-based Phenomena
Some clocking behaviors, such as counters and integrators etc.
Collaborative Phenomena
Some of us have a great interest in some form of emergent phenomena and group dynamics based on simple local rules and external stimulae. Examples would be behaviors like sorting, pattern detections, flocking etc.
Development Groups
We decided to cluster related projects and to form groups which will dedicate their time to this cluster. The goal is to converge to some single preferred solution based on these project ideas while keeping an eye on feasability, coolness, usefulness, and modular architecture on the way.
If you are in no group yet, please choose one.
Quorum Sensing based (Dominic, Giorgia, Herve)
Oscillator based (Urs, Christophe, Jonas)
Generation based (-)
Other projects (Jonas, Simon, Dominic)
Merged Projects
The two projects below are the outcome of the work of our two remaining development groups. They both have their pros and cons and the discussion continues until at least Monday evening.
- Project X aka "SO-Constructor" by the development group for the Quorum_Sensing_based projects.
- Counter aka "The Thing" by the corresponding development group for Oscillator_based projects.
Ballot
Please everybody make your vote (1 means "forget it" and 10 means "definitely a Nature paper") on the four criteria.
Constructor (aka Project X)
CONSTRUCTOR | Urs | Tamara | Jonas | Zlatko | Giorgia | Simon | Kristian | Herve | Dominic | Alexander | Christophe | Robin |
Usefulness | 6 | 4 | - | 7 | - | 6 | - | - | - | - | - | 7 |
Feasability | 4 | 8 | - | 6? | - | 5 | - | - | - | - | - | 6 |
Modularity | 10 | 8 | - | 10 | - | 9 | - | - | - | - | - | 7 |
Coolness | 9 | 7 | - | 10 | - | 9 | - | - | - | - | - | 8 |
Additional Comments:
Tamara: As an engineer, I think the counter is completely useful and totally cool as well. I'm really excited at the prospect that it might actually work (which I frankly still doubt a little bit at the moment). The SO-Constructor definitely is cool as well, but I don't see it's usefulness yet, but as I'm no bilogist, it is not mine to judge. Talking about modularity, I see that the SO-Constructor has a lot of modules, but they are not 'parallel' modules, but 'serial' modules, i.e. if one module fails, the overlaying modules won't work as well. They strongly depend on each other. I also see the problem of tuning, because there is a real lot of tuning to do and nearly everything needs to be tuned. For me, some questions arise like: Can you simply change the threshold for a certain protein in quorum sensing? Anyway, the probability that we have some results to present in the end is still relatively high. I don't think the counter is really modular, altough it is a combination of one basic part (the 'thing'). The point is, if that basic part works, the whole counter probably works as well. If it doesn't, then we don't have anything at all. But shouldn't we just take the risk and try it? No risk, no fun :-) Conclusion: The SO-Constructor is in my opinion the 'safer' option, meaning that we are much more probable to get something that actually works. Whereas the Counter is much more useful and revolutionary, at least when we get to work it somehow.
Dominic: As I already have said during the meeting, I am a little bit concerned about the effects of the different presentation styles and levels of detail: it is hard to judge the feasability of one or the other, since for the SO-Constructor I can see a clear stepwise approach with controllable biological units to implement, but I am doubtful about the tuning and proper interplay of all these components - although I am confident that to some degree this can be achieved. As for the Counter I am also not sure about the basic biological assumptions, e.g. whether the toggle switch units are available and will work as well as the symmetric repression/activation that is necessary, although the modeling part suggests everything is straightforward - but this might be deceiving. It is hard for me to judge the biological unpredictabilites and risks, but from an engineering point of view the Counter building block is of the more useful thing to do, since it has a broad application range thanks to the clear interfaces. Last but not least such a technical unit seems more suitable in the context of Synthetic Biology.
Urs: I think if the whole thing works this project is astonishing. But I'm in doubt about it. The fact that you could model each step seperatly is of course a big advantage of this project. The probability that at least a few of the steps work is quite high and so you will see some results at the end. I'm not so sure about the usefulness. To encapsulate some bacterias which produce a certain substance could be usefull but I'm not an expert in this stuff.
Zlatko: I like the general idea and concept of the SO-Constructor project very much, even if many team members expressed their doubts about the practical benefits (as Urs mentioned above it could be used for substance (e.g. drug) encapsulation. I'm not sure, but I think that one may also use the whole thing for detection and localization purposes (e.g. of toxic substances)). As others pointed out already, overall feasibility, especially the expected difficulties in connecting the different modules, could be a drawback here. Dominic, Giorgia and Herve have really elaborated an excellent model, but to me it seems to be very complex and I don't know if we could manage to set the whole thing up in time (on the other hand this does not seem to be a general concern because of the "intermediate results"). But since my knowledge of (applied) molecular biology is very limited and I don't know how (non-)volatile the counter circuit is, my personal feasibility estimation stands on thin soil.
Hervé: The presentations made on Thursday had a different profile in terms of details and analysis. It is obvious that the constructor group had focused its energy on the feasibility and the options available to circumvent the problems that will arise during the development of this project. It is also clear that we refused to present the details about all these options because we wanted to discuss about the concept only. I would recommend people having some doubts about the feasibility to check the detailed information available on the wiki. Concerning the usefulness, I do think that both projects are extremely useful and I have some problems to understand that people are questioning the usefulness of the constructor bacteria project (sorting and purification is a key issue for biotech companies for example).In order to make the appropriate choice, I would still need more information about the availability of the modules involved in the "thing" project. Do we really have the repressors and activators required for this project? Which ones are we gonna use? Considering that it is dificult to have activators and repressors with the same "strenght", how could this affect the model and the feasibility of the "thing" project? It is really interesting to notice that people have better feeling about the feasibility of this project (compared to the constructor bacteria) even though the biology part (which is, in the end, the core and working part of the project)has been more or less skipped during the "thing" presentation.Regarding the concept of the synthetic biology, I have to agree that the "thing" project sounds much more appropriate for this kind of competition. This would be in the end the criteria that would push my vote into this project (after a deeper analysis of the feasibility and availability of the needed activators and repressors).If we decide to go for this project we can of course reduce the risk factor by taking different activator - repressor candidates and maybe trying 2 or 3 combinations that have passed through the modelization test.
Christophe: Herve, we have not looked for actual repressors/activators because we believe that we should first concentrate on the design, at the "functionality" level so to say. Now that that part is more or less clear, well yes, you are right, we should start looking at the implementation. And when I say "we", that's everybody, and in particulary you and those who have more experience in the lab. I just had a quick look at pubmed, and i found a paper that mentions a protein ("TyrR") that acts as repressor and activator (see ref below). Another potential protein is "Cra", that can activate or repress depending where it binds to the DNA. Maybe we can work with a fusion protein from an activator and a repressor. Maybe we can solve the duality by using an activator that is required for the expression of genes 1/3 but represses genes 2/4, that are otherwise expressed constitutively, by placing its binding site at a position that overlaps with the polymerase binding sites, etc... What are *your* suggestions? Can you look into that issue? Don't you think we can solve that problem?
Refs: [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1943694&dopt=Citation TyrR protein of Escherichia coli and its role as repressor and activator.]
[http://jb.asm.org/cgi/reprint/178/12/3411?view=reprint&pmid=8655535 The catabolite repressor/activator (Cra) protein of enteric bacteria]
Counter (aka The Thing)
COUNTER | Urs | Tamara | Jonas | Zlatko | Giorgia | Simon | Kristian | Herve | Dominic | Alexander | Christophe | Robin |
Usefulness | 10 | 10 | - | 9 | - | 8 | - | - | - | - | - | 10 |
Feasability | 6 | 7 | - | 7? | - | 7 | - | - | - | - | - | 7 |
Modularity | 7 | 5 | - | 5 | - | 8 | - | - | - | - | - | 9 |
Coolness | 8 | 10 | - | 9 | - | 9 | - | - | - | - | - | 9 |
Additional Comments:
Urs: From the engineer's point of few a counter like this is of course a crucial brick. As you can take the concentration of any substance you like (by transforming it to our input S) and also add for every single counter step a specific gene needed for an application this counter can be used whereever you want. The big disadvantage is of course that if the counter doesn't work there will be no result you can see.
Christophe: About feasibility: i don't agree with much of what has been said here. The counter is made of two toggle switches. These switches exist in the nature (lambda repressor) and have also been synthetized (Gardner et al., partly also on MIT registry). Now, the only things we need to come up with are A) a way of having 4 different types of road blocks, which is, as Sven said, possible using zinc-fingers that target different dna seqs, and B) a way to have S working as an inducer and as a repressor, in a roughly symmetrical manner. And that's all. I am not saying that it is trivial, but seriously, it is really doable. And even if we don't manage it to do it for the jamboree, finishing it later could still be academically very rewarding. Bottom line: The difference between the two projects, i guess, is that most of the work in the QS project would be at the assembling/tuning of existing parts for a very cool final effect, while in the the counter, we would focus the energy of the whole group into realizing a little module that is reliable and reusable. Both projects are cool, both teams have done an increadible amount of preparatory work until now and so at this point, i would be very excited working on either projects.
Zlatko: A stable counter would be a very nice thing to have. In my eyes this project seems to be a bit more feasible, but maybe that's a misjudgement. The model as elaborated by the group is detailed and the simulation seems to be quite promising. On the other hand the "all-or-nothing" scenario makes it a bit risky. PS: even though I didn't give a 10 for coolness, I do believe that it's a Nature candidate.
External Information
Links
Papers
bulter04, atkinson03, bates05, keiler01, suetsugu03, sudesh00, römling02, ross91, sutherland01, Lai04, zogaj01, miller01, basu05, goryachev05,
you04,