Paris/Modeling
From 2007.igem.org
| Line 1: | Line 1: | ||
| - | + | MODELIZATION OF THE SYNTHETIC ORGANISME | |
[[Paris_Modeling_fr|French Page]] | [[Paris_Modeling_fr|French Page]] | ||
| Line 15: | Line 15: | ||
| - | == | + | ==Rythme and organise the biological constructs== |
| - | + | We need to [http://openwetware.org/wiki/Parts_characterization/Characterization_approaches caracterise] the biobricks we're about to use, BEFORE assembling them, so that we can feed the model with parameter values. The We use the model to construct, and see if it fits or not the model, and try to understand why. (It's a new way of research in biology : instead of tearing complicated system a part, you try to first build simple ones, and by observing the difference with theory, a new explanation will sharpen the model | |
| - | = | + | =Model WHAT ?= |
| - | == | + | ==Macroscopic Modelization == |
| - | + | By macroscopique, I mean the modelization at cellular cultur level, with parameter that you can measure outside the cell. | |
| - | + | We need to get the parameter input and output values of the different elements of the system, introduce them in the model, get the desired cre lox transformation rate, and modifie the cre promoteur, or it's RBS by using caracterised biobricks. | |
| - | + | Parameters to look for in the litterature then to [http://openwetware.org/wiki/Parts_characterization/Measurement_techniques measure] in vitro by ourself : | |
| - | *Absorbtion | + | *Absorbtion of the vital AA by a cell |
| - | *Production | + | *Production of the vital AA by a cell |
| - | * | + | *Diffusion zone of the AA |
| - | * | + | *Lethal width of a cell without FTSZ ( for a AA producing cell) (how do you measure it? cell cycle? 4 OR 5 says Ariel. Same cycle speed as for a normal cell (without FTSZ)? |
| - | * | + | *Lethal width of a cell without FTSZ ( for a triglyceride producing cell)? |
| - | + | *Cre lox recombination rate | |
| + | Always try to use a reference promoteur or RBS for the caracterisation | ||
| - | |||
| - | + | ==Microscopique or Genetic Modelization == | |
| - | == | + | It's the modelisation of what happens IN the cell : of the genetic network, with the quantity of the different proteins as parameter |
| - | + | How can we measure the moduls'efficiency? Thanks to [http://parts2.mit.edu/r/parts/htdocs/AbstractionHierarchy/ Pops] and Rips (Ribosome per seconde). We need reference unity measures. For the [http://partsregistry.org/partsdb/pgroup.cgi?pgroup=RBS Ribosome binding site], we should always compare the RBS used to [http://partsregistry.org/Part:BBa_B0034 this one]. Is it also possible to have a reference promotor? | |
| - | + | ||
| - | + | ||
Revision as of 17:32, 1 July 2007
MODELIZATION OF THE SYNTHETIC ORGANISME
What do we want to do ? The goal is to model the cellular growth, and to prove it is possible, to find the range of paramaters that enables it, and then to optimise the triglycerid production. Is it Possible for a cell producing the Amino Acide, to feed at the same time the mother cell, and the triglyciride factory one? For this, we need to find the good theoritical balance between the different elements of the population. This balance is determined by the firing rate of the cre/lox system, which is genetically engineered
Contents |
Why a modélisation ?
Minimise the biological steps
Make the system work by finding the possible parameters, and save time when doing wetwork, in order to directly make make the construct the most likely to work. ( For instance, immediately use the good promoters or RBS) Some might say the system is "simple enough" to build, so that it can be hand crafted. It might work so. But if we don't try to model a simple system, and try to make it stick as much as possible to reality, how can we ever hope to do it for a more complex one?
Biosynthetic spirit IGEM
If you listen toEndy,biosynthetic is not making a biological construct. It's HOW you make it, it's the process you use to build it. It's giving the possibility to first virtually create the system before carrying it out: by assembling the biobricks as judiciously as possible, by exactly knowing the link between input and ouput. It has to be reflected in the construction process.
Rythme and organise the biological constructs
We need to caracterise the biobricks we're about to use, BEFORE assembling them, so that we can feed the model with parameter values. The We use the model to construct, and see if it fits or not the model, and try to understand why. (It's a new way of research in biology : instead of tearing complicated system a part, you try to first build simple ones, and by observing the difference with theory, a new explanation will sharpen the model
Model WHAT ?
Macroscopic Modelization
By macroscopique, I mean the modelization at cellular cultur level, with parameter that you can measure outside the cell. We need to get the parameter input and output values of the different elements of the system, introduce them in the model, get the desired cre lox transformation rate, and modifie the cre promoteur, or it's RBS by using caracterised biobricks.
Parameters to look for in the litterature then to measure in vitro by ourself :
- Absorbtion of the vital AA by a cell
- Production of the vital AA by a cell
- Diffusion zone of the AA
- Lethal width of a cell without FTSZ ( for a AA producing cell) (how do you measure it? cell cycle? 4 OR 5 says Ariel. Same cycle speed as for a normal cell (without FTSZ)?
- Lethal width of a cell without FTSZ ( for a triglyceride producing cell)?
- Cre lox recombination rate
Always try to use a reference promoteur or RBS for the caracterisation
Microscopique or Genetic Modelization
It's the modelisation of what happens IN the cell : of the genetic network, with the quantity of the different proteins as parameter How can we measure the moduls'efficiency? Thanks to Pops and Rips (Ribosome per seconde). We need reference unity measures. For the Ribosome binding site, we should always compare the RBS used to this one. Is it also possible to have a reference promotor?
