Difference between revisions of "Chassis/Cell-Free Systems"
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==Introduction== | ==Introduction== | ||
+ | '''Cell-Free Systems (CFS)''' involve the in-vitro expression of genes into proteins. These systems can serve as a compatible chassis for the various parts and devices from the Registry of Standard Biological Parts. | ||
− | + | Coupled transcription-translation systems usually combine a bacteriophage RNA polymerase and promoter with eukaryotic or prokaryotic extracts. In addition, the PURE system has been developed as a reconstituted CFS for synthesizing proteins using recombinant elements. | |
− | + | <br> | |
− | + | <br> | |
− | + | '''Advantages and disadvantages of CFS''' | |
+ | {| border="1" | ||
+ | |- | ||
+ | |width=50%|<center>'''Advantages'''</center> | ||
+ | |width=50%|<center>'''Disadvantages'''</center> | ||
+ | |- | ||
+ | |style="background:#eeffee"|Non-infectious because of non-proliferative nature | ||
+ | |style="background:#ffeeee"|Short expression lifespan since system cannot replicate | ||
+ | |- | ||
+ | |style="background:#eeffee"|Process is quick and simple requiring only preparation of cell extract and feeding solution and subsequent addition of DNA template | ||
+ | |style="background:#ffeeee"|Expensive because of the constant need for nutrient and energy supply | ||
+ | |- | ||
+ | |style="background:#eeffee"|Quality control can be achieved easily using modified reaction conditions such as addition of accessory elements or inhibitory factors | ||
+ | |style="background:#ffeeee"|Less characterization and experience of use in the laboratories compared to ''E. coli'' | ||
+ | |} | ||
+ | <br> | ||
+ | '''Specifications for CFS characterization'''<br> | ||
+ | The following are several parameters that will help us understand the advantages and disadvantages associated with a particular chassis housing the gene expression machinery. | ||
+ | {| border="1" | ||
+ | |- | ||
+ | |style="background:#ffffcc"|'''Properties''' | ||
+ | ||<center>'''Definitions'''</center> | ||
+ | |- | ||
+ | |style="background:#ffffcc"|Rise time | ||
+ | ||Measure of time from start of reaction to the point when expression rate first reaches the steady state value. | ||
+ | |- | ||
+ | |style="background:#ffffcc"|Peak time | ||
+ | ||Measure of time from start of reaction to the point when expression rate reaches the maximum value. | ||
+ | |- | ||
+ | |style="background:#ffffcc"|Settling time | ||
+ | ||Measure of time from start of reaction to the point when expression rate reaches the steady state and does not escape from it for a prolonged period of time. | ||
+ | |- | ||
+ | |style="background:#ffffcc"|Stability of synthesized protein | ||
+ | ||Measure of the half-life of a given protein (e.g. GFP) in the chassis. | ||
+ | |- | ||
+ | |style="background:#ffffcc"|Total expression capacity | ||
+ | ||Measure of the total expression of a chassis for a given DNA construct template. This should take into account the degradation of synthesized protein. | ||
+ | |- | ||
+ | |style="background:#ffffcc"|Expression lifespan | ||
+ | ||Measure of time that expression occurs for a given DNA construct template until protein degradation overrides protein synthesis. | ||
+ | |- | ||
+ | |} | ||
==Cell-Free Systems investigated== | ==Cell-Free Systems investigated== |
Revision as of 22:32, 20 October 2007
Cell-Free Systems
Introduction
Cell-Free Systems (CFS) involve the in-vitro expression of genes into proteins. These systems can serve as a compatible chassis for the various parts and devices from the Registry of Standard Biological Parts.
Coupled transcription-translation systems usually combine a bacteriophage RNA polymerase and promoter with eukaryotic or prokaryotic extracts. In addition, the PURE system has been developed as a reconstituted CFS for synthesizing proteins using recombinant elements.
Advantages and disadvantages of CFS
Non-infectious because of non-proliferative nature | Short expression lifespan since system cannot replicate |
Process is quick and simple requiring only preparation of cell extract and feeding solution and subsequent addition of DNA template | Expensive because of the constant need for nutrient and energy supply |
Quality control can be achieved easily using modified reaction conditions such as addition of accessory elements or inhibitory factors | Less characterization and experience of use in the laboratories compared to E. coli |
Specifications for CFS characterization
The following are several parameters that will help us understand the advantages and disadvantages associated with a particular chassis housing the gene expression machinery.
Properties | |
Rise time | Measure of time from start of reaction to the point when expression rate first reaches the steady state value. |
Peak time | Measure of time from start of reaction to the point when expression rate reaches the maximum value. |
Settling time | Measure of time from start of reaction to the point when expression rate reaches the steady state and does not escape from it for a prolonged period of time. |
Stability of synthesized protein | Measure of the half-life of a given protein (e.g. GFP) in the chassis. |
Total expression capacity | Measure of the total expression of a chassis for a given DNA construct template. This should take into account the degradation of synthesized protein. |
Expression lifespan | Measure of time that expression occurs for a given DNA construct template until protein degradation overrides protein synthesis. |
Cell-Free Systems investigated
- Home-made E.Coli T7 S30 Extract
- Home made E.Coli S30 Extract
- Commercial E.Coli S30 Extract
- Vesicles ...
References
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