Difference between revisions of "Part:BBa K771007"

 
(Constitutive Aggregation)
 
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K771007 short</partinfo>
 
<partinfo>BBa_K771007 short</partinfo>
  
Membrane anchor 1, which consists of interacting domain and membrane protein Lgt
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Membrane anchor 2 (without MS2) consists of SH3 domain([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771107 BBa_K771107]) and membrane protein Lgt([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771102 BBa_K771102]).
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==Overview: Membrane Scaffold System (without signal induction)==
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[[Image:12SJTU-MA2-MA5.png|500px|center]]
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Demonstration of the ''Membrane Scaffold'' device (without signal induction). Membrane Anchor 2 (without MS2), 3, 4, 5(without VVD) consitutively aggregate together.
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==Backgroud==
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===Constitutive Aggregation===
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Membrane Anchor 2 without MS2 and Membrane Anchor 3 constitutively aggregate through SH3 domain([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771107 BBa_K771107]) and SH3 ligand ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771108 BBa_K771108]).
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[[Image:12SJTU_CA11wm.png|250px|center]]
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==Design==
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[[Image:12SJTU_MA2wm.png|200px|center]]
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Membrane protein Lgt ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771102 BBa_K771102]) and SH3 domain([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771107 BBa_K771107]). It is expected to constitutively aggregate with Membrane Anchor 3.
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==Characterization==
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To testify the constitutive aggregation of Membrane Anchor 2 without MS2 and Membrane Anchor 4, we conducted Fluorescence Complementation Assay.
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In fluorescence complementation assay, proteins that are postulated to interact are fused to unfolded complementary fragments of EGFP and expressed in ''E.coli''. Interaction of these proteins will bring the fluorescent fragments within proximity, allowing the reporter protein to reform in its native three-dimensional structure and emit its fluorescent signal. EGFP was split into two halves, named split EGFP1 ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771113 BBa_K771113]) and split EGFP 2([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771114 BBa_K771114]) respectively. If there is interaction between two proteins which were fused with 1EGFP and 2EGFP, it is expected that fluorescence should be observed. Otherwise, no fluorescence could be observed.
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===Membrane Anchor 2 without MS2 and Membrane Anchor 3===
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[[Image:12SJTU-MA23.png|center|500px]]
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[[Image:12SJTU Anchor GFP.jpg|450px|center]]
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We fused split EGFP 1 and 2 to Membrane Anchor 2 without MS2 and Membrane Anchor 3 to test whether Membrane Anchor 2 without MS2 and Membrane Anchor 3 could constitutively aggregate. Proteins in control group are not expected to aggregate like in experimental group.We coexpressed proteins in experimental group and control group respectively in ''E.coli''. After induction for 6 hours, bacteria samples were taken for fluorescence observation.
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The result shows that Membrane Anchor 2 without MS2 and Membrane Anchor 3 could constitutively aggregate through SH3 domain and ligand.
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==Application==
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We recruired fatty acid biosynthetic pathway involving TesA([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771301 BBa_K771301]), FabG([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771302 BBa_K771302)]) , FabI([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771303  BBa_K771303]), FabZ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771304 BBa_K771304]) to put our membrane scaffold system into practice. Fatty Acid productivity is enhanced by 24 fold.
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We constructed TesA with Membrane Anchor 2 (without MS2) ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771305 BBa_K771305]),FabG with Membrane Anchor 3,([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771306 BBa_K771306]), FabZ with Membrane Anchor 4 ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771307 BBa_K771307]), FabI with Membrane Anchor 4(without VVD )([https://parts.igem.org/wiki/index.php?title=Part:BBa_K771308 BBa_K771308]). Click into each part for more infomation.
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[[Image:12SJTU-FATTYACID.png|400px|center]]
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==Related Biobrick==
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<br\>Membrabe Anchor 3([[https://parts.igem.org/wiki/index.php?title=Part:BBa_K771003 BBa_K771003]])
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<br\>Membrabe Anchor 4([[https://parts.igem.org/wiki/index.php?title=Part:BBa_K771004 BBa_K771004]])
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<br\>Membrabe Anchor 5 without VVD([[https://parts.igem.org/wiki/index.php?title=Part:BBa_K771008 BBa_K771008]])
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==Reference==
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Dueber, J. E., G. C. Wu, et al. (2009). "Synthetic protein scaffolds provide modular control over metabolic flux." Nature biotechnology 27(8): 753-759.
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 05:16, 2 October 2012

Membrane Anchor 2 without MS2:ssDsbA-LGT-SH3 Domain


Membrane anchor 2 (without MS2) consists of SH3 domain(BBa_K771107) and membrane protein Lgt(BBa_K771102).

Overview: Membrane Scaffold System (without signal induction)

12SJTU-MA2-MA5.png

Demonstration of the Membrane Scaffold device (without signal induction). Membrane Anchor 2 (without MS2), 3, 4, 5(without VVD) consitutively aggregate together.

Backgroud

Constitutive Aggregation

Membrane Anchor 2 without MS2 and Membrane Anchor 3 constitutively aggregate through SH3 domain(BBa_K771107) and SH3 ligand (BBa_K771108).

12SJTU CA11wm.png

Design

12SJTU MA2wm.png

Membrane protein Lgt (BBa_K771102) and SH3 domain(BBa_K771107). It is expected to constitutively aggregate with Membrane Anchor 3.

Characterization

To testify the constitutive aggregation of Membrane Anchor 2 without MS2 and Membrane Anchor 4, we conducted Fluorescence Complementation Assay.

In fluorescence complementation assay, proteins that are postulated to interact are fused to unfolded complementary fragments of EGFP and expressed in E.coli. Interaction of these proteins will bring the fluorescent fragments within proximity, allowing the reporter protein to reform in its native three-dimensional structure and emit its fluorescent signal. EGFP was split into two halves, named split EGFP1 (BBa_K771113) and split EGFP 2(BBa_K771114) respectively. If there is interaction between two proteins which were fused with 1EGFP and 2EGFP, it is expected that fluorescence should be observed. Otherwise, no fluorescence could be observed.

Membrane Anchor 2 without MS2 and Membrane Anchor 3

12SJTU-MA23.png
12SJTU Anchor GFP.jpg

We fused split EGFP 1 and 2 to Membrane Anchor 2 without MS2 and Membrane Anchor 3 to test whether Membrane Anchor 2 without MS2 and Membrane Anchor 3 could constitutively aggregate. Proteins in control group are not expected to aggregate like in experimental group.We coexpressed proteins in experimental group and control group respectively in E.coli. After induction for 6 hours, bacteria samples were taken for fluorescence observation. The result shows that Membrane Anchor 2 without MS2 and Membrane Anchor 3 could constitutively aggregate through SH3 domain and ligand.

Application

We recruired fatty acid biosynthetic pathway involving TesA(BBa_K771301), FabG(BBa_K771302)) , FabI(BBa_K771303), FabZ(BBa_K771304) to put our membrane scaffold system into practice. Fatty Acid productivity is enhanced by 24 fold.

We constructed TesA with Membrane Anchor 2 (without MS2) (BBa_K771305),FabG with Membrane Anchor 3,(BBa_K771306), FabZ with Membrane Anchor 4 (BBa_K771307), FabI with Membrane Anchor 4(without VVD )(BBa_K771308). Click into each part for more infomation.

12SJTU-FATTYACID.png



Related Biobrick

<br\>Membrabe Anchor 3([BBa_K771003]) <br\>Membrabe Anchor 4([BBa_K771004]) <br\>Membrabe Anchor 5 without VVD([BBa_K771008])

Reference

Dueber, J. E., G. C. Wu, et al. (2009). "Synthetic protein scaffolds provide modular control over metabolic flux." Nature biotechnology 27(8): 753-759.


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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 883
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 504
    Illegal SapI.rc site found at 1150