Difference between revisions of "Chassis/Cell-Free Systems"

Revision as of 12:30, 22 October 2007

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 1.

Advantages and disadvantages of CFS

Advantages	Disadvantages
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
Several parameters are identified to help us understand the advantages and disadvantages associated with using a particular chassis.

Properties	Definitions
Optimum temperature	Temperature at which expression rate reaches a maximum value.
Peak time	Measure of time from start of reaction to the point when expression rate reaches the maximum value.
Product stability	Measure of the half-life of a given protein (e.g. GFP) synthesized in the chassis.
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

Please click on each system for its individual characterization.

Homemade E. coli S30

Commercial E. coli S30

Commercial E. coli T7 S30

Vesicle-encapsulation

Different compartmentalization strategies

Batch-mode	Transcription-translation reaction is carried out in bulk solution.
Continuous-exchange	Transcription-translation reaction is separated from feeding solution by a dialysis membrane.
Vesicle-encapsulated	The reaction is separated from feeding solution by a phospholipid bilayer. More reliable exchange of materials is established by inserting a non-specific pore protein into the phospholipid bilayer.2

DNA constructs selected for CFS characterization

A simple constitutive gene expression device that reguires an E. coli RNA polymerase BBa_I13522
A simple constitutive gene expression device that requires a T7 bacteriophage RNA polymerase BBa_R0085
An inducible gene expression device that is well-characterized in the registry BBa_T9002

References

1 pmid=16076456
2 pmid=16224117
3 pmid=14559971
4 pmid=15183761

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@@ Line 74: / Line 74: @@
 '''DNA constructs selected for CFS characterization'''
 *A simple constitutive gene expression device that reguires an ''E. coli'' RNA polymerase [https://parts.igem.org/wiki/index.php/Part:BBa_I13522 BBa_I13522]
-*A simple constitutive gene expression device that requires a T7 bacteriophage RNA polymerase [https://parts.igem.org/wiki/index.php/Part:BBa_E7104 BBa_E7104]
+*A simple constitutive gene expression device that requires a T7 bacteriophage RNA polymerase [https://parts.igem.org/wiki/index.php/Part:BBa_R0085 BBa_R0085]
 *An inducible gene expression device that is well-characterized in the registry [https://parts.igem.org/wiki/index.php/Part:BBa_T9002 BBa_T9002]
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