Difference between revisions of "Part:BBa K2933252"
Line 19: Line 19:
  
 
===Usage and Biology===
 
===Usage and Biology===
−
This composite part is made up with three basic parts, the GST tag, the cutting site of Prescission Protease and our target protein MUS-2. It encodes a protein which is MUS-2 fused with GST tag. The fusion protein is about 54.3 kD. In order to gain the highly purified target protein, we add GST tag in N-terminal of MUS-2 and combine the two parts with the cutting site of Prescission Protease. The fusion protein can be cut off at the cutting site by Prescission Protease. It is convenient for us to purify our target protein.<br>
+
This composite part is made up with eight basic parts, T7 Ribosome binding sites, the His-Sumo tag, three cutting sites of Prescission Protease, our target protein MUS-2 and T7 terminator. It encodes a protein which is MUS-2 fused with His-Sumo tag. The fusion protein is about 40.3 kD. The fusion protein can be cut off at the cutting sites by Prescission Protease. It is convenient for us to purify our target protein.<br>
  
 
===Molecular cloning===
 
===Molecular cloning===
−
We used the vector pGEX-6p-1 to construct our expression plasmid.  
+
We used the vector PET-28bs to construct our expression plasmid.  
 
<p style="text-align: center;">
 
<p style="text-align: center;">
 
   [[File:TJUSLS China--MUS-2-PCR.png|500px]]<br>
 
   [[File:TJUSLS China--MUS-2-PCR.png|500px]]<br>

Revision as of 13:14, 22 September 2019


RBS b+Linker h+His+Linker a+Sumo+Linker b+MUS-2+T7 terminator

This part consists of RBS, protein coding sequence(His+Linker a+Sumo+Linker b+MUS-2) and T7 terminator,and the biological module can be build into E.coli for protein expression. This part can be prefaced with promoters of different strengths and types to regulate expression function.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 298
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 298
    Illegal NheI site found at 75
    Illegal NheI site found at 1146
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 298
    Illegal BglII site found at 187
    Illegal BamHI site found at 386
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 298
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 298
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

This composite part is made up with eight basic parts, T7 Ribosome binding sites, the His-Sumo tag, three cutting sites of Prescission Protease, our target protein MUS-2 and T7 terminator. It encodes a protein which is MUS-2 fused with His-Sumo tag. The fusion protein is about 40.3 kD. The fusion protein can be cut off at the cutting sites by Prescission Protease. It is convenient for us to purify our target protein.

Molecular cloning

We used the vector PET-28bs to construct our expression plasmid.

TJUSLS China--MUS-2-PCR.png
Figure 1. Left: The PCR result of MUS-2. Right: The verification results by enzyme digestion.

After verification, it was determined that the construction is successful.