Difference between revisions of "Part:BBa K5301014"

(Characterization)
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==Characterization==
 
==Characterization==
  
We performed an in vitro mixing and incubation of sGFP1-10 with sGFP11 to achieve their binding(in the form of sGFP1-10/11 tether <partinfo>BBa_K5301017</partinfo><partinfo>BBa_K5301018</partinfo>). The images captured under a fluorescence microscope are shown in the figure below.
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We performed an in vitro mixing and incubation of sGFP1-10 with sGFP11 to achieve their binding(in the form of sGFP1-10 tether <partinfo>BBa_K5301017</partinfo>and sGFP11 tether<partinfo>BBa_K5301018</partinfo>). The images captured under a fluorescence microscope are shown in the figure below.
  
  
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==Sequence and Features==
 
==Sequence and Features==
 
<partinfo>BBa_K5301014 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K5301014 SequenceAndFeatures</partinfo>

Revision as of 08:40, 2 October 2024


sGFP11 is an engineered version of the final strand of the GFP beta-barrel.


sGFP11 is the smaller fragment of the Split-GFP system, encompassing the final β-strand domain of green fluorescent protein (GFP).The isolated GFP11 fragment does not fluoresce on its own and is typically fused to the C-terminus of the target protein. Upon binding with the GFP1-10 fragment(BBa_K5301012), it facilitates the restoration of GFP's fluorescent activity.


Usage and Biology

In our team's experiments, sGFP1-10 and sGFP11 are individually fused and expressed with the target proteins.We use the self-assembly of GFP1-10 and GFP11 to construct membrane protein dimers.


Characterization

We performed an in vitro mixing and incubation of sGFP1-10 with sGFP11 to achieve their binding(in the form of sGFP1-10 tether BBa_K5301017and sGFP11 tetherBBa_K5301018). The images captured under a fluorescence microscope are shown in the figure below.


sgfp-fluorescent.png

Figure 1.Fluorescence images following the reassembly of sGFP(4×10).Figure A and Figure C represent the background fluorescence, while Figures B and D show the observations after the addition of the samples at corresponding positions. By comparing these results, the corresponding fluorescence signals are obtained to eliminate false positives.


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]