Difference between revisions of "Part:BBa K174002"

 
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<partinfo>BBa_K174002 short</partinfo>
 
<partinfo>BBa_K174002 short</partinfo>
  
The purpose of this part is to control the expression of sspB, the degradation controller.  
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The purpose of this part is to selectively control the rate of degradation of proteins in ''Bacillus subtilis''.
  
Mutations on ssrA degradation tags weakens the recognition of the tagged protein by ClpX. Modified versions require sspB adaptor protein for the degradation. Hence when sspB protein is expressed, the proteins tagged with modified version of ssrA tag are targeted for degradation, otherwise they remain stable (1).
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Griffith and Grossman, 2008 [1], showed that by tagging proteins with ''ssrA'' tags they can be tagged for recruitment by ClpX and subject to proteolysis.  
  
This device is inducible by arabinose, therefore we can alter the arabinose levels to regulate the degradation of proteins tagged with the modified version of ssrA degradation tags.
+
Mutations on ''ssrA'' degradation tags weaken the recognition of the tagged protein by ClpX. Modified versions require SspB adaptor protein for transport to ClpX and subsequent degradation. Hence when SspB protein is expressed, the proteins tagged with modified version of ''ssrA'' tag are targeted for degradation, otherwise they remain stable [1].
  
 +
This device is inducible by arabinose, therefore we can alter the arabinose levels to regulate the degradation of proteins tagged with the modified version of ''ssrA'' degradation tags.
  
Wild type E. coli ssrA tag is AANDENY-ALAA (SspB recognition site – ClpX recognition site).
 
  
As an example of the tag, we constructed [[Part:BBa_K174003]] with Hin tagged with the modified version of ssrA tag below.
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The wild type ''E. coli'' ssrA tag is AANDENY-ALAA (SspB recognition site – ClpX recognition site).
  
AANDENY-SENY-ALGG (SspB recognition site – SENY +4 Linker - ClpX recognition site)
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As an example of the tag, we constructed [[Part:BBa_K174003]] with Hin protein which was tagged with the modified version of ''ssrA'' tag below.
  
However, it should also be noted that different degradation tags may have effect on the activity of different proteins (1).
+
AANDENY-SENY-ALGG (SspB recognition site – SENY +4 Linker - ClpX recognition site)  
  
For more information about this part, go to Newcastle iGEM2009 [http://2009.igem.org/Team:Newcastle/Stochasticity Stochasticity] and [http://2009.igem.org/Team:Newcastle/Modelling Modelling] pages.
+
However, it should also be noted that different degradation tags may have effect on the activity of different proteins [1]. For more information about this part, go to Newcastle iGEM 2009 [http://2009.igem.org/Team:Newcastle/Stochasticity Stochasticity] and [http://2009.igem.org/Team:Newcastle/Modelling Modelling] pages.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 23:12, 21 October 2009

Arabinose controlled protein degradation device

The purpose of this part is to selectively control the rate of degradation of proteins in Bacillus subtilis.

Griffith and Grossman, 2008 [1], showed that by tagging proteins with ssrA tags they can be tagged for recruitment by ClpX and subject to proteolysis.

Mutations on ssrA degradation tags weaken the recognition of the tagged protein by ClpX. Modified versions require SspB adaptor protein for transport to ClpX and subsequent degradation. Hence when SspB protein is expressed, the proteins tagged with modified version of ssrA tag are targeted for degradation, otherwise they remain stable [1].

This device is inducible by arabinose, therefore we can alter the arabinose levels to regulate the degradation of proteins tagged with the modified version of ssrA degradation tags.


The wild type E. coli ssrA tag is AANDENY-ALAA (SspB recognition site – ClpX recognition site).

As an example of the tag, we constructed Part:BBa_K174003 with Hin protein which was tagged with the modified version of ssrA tag below.

AANDENY-SENY-ALGG (SspB recognition site – SENY +4 Linker - ClpX recognition site)

However, it should also be noted that different degradation tags may have effect on the activity of different proteins [1]. For more information about this part, go to Newcastle iGEM 2009 [http://2009.igem.org/Team:Newcastle/Stochasticity Stochasticity] and [http://2009.igem.org/Team:Newcastle/Modelling Modelling] pages.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


References

  1. Griffith, K. L., and A. D. Grossman. 2008. Inducible protein degradation in Bacillus subtilis using heterologous peptide tags and adaptor proteins to target substrates to the protease ClpXP. Mol. Microbiol. 70:1012-1025.