Difference between revisions of "Part:BBa K1119000"

 
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<partinfo>BBa_K1119000 short</partinfo>
 
<partinfo>BBa_K1119000 short</partinfo>
  
Mitochondrial leader sequence (MLS) helps direct protein to the mitochondria. When this sequence is cloned in frame at the N-terminus of the protein, it can target the recombinant protein to the mitochondria in mammalian cells. MLS will be removed upon translocation into the mitochondrial matrix. However, at least four additional amino acids (Ile-His-Ser-Leu) on this sequence are known to be retained on the N-terminus of the protein.  
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Mitochondrial Leader Sequence (MLS) helps direct protein to the mitochondria when this peptide sequence is in front of the N-terminus of the protein of interest. MLS will be removed upon the peptide’s translocation into the mitochondria, but four additional amino acid residues (Ile-His-Ser-Leu) will be left at the N-terminus of the protein. (Invitrogen, Carlsbard, CA)  Under the RFC25 standard, two additional amino residue linker (Ala-Gly) will be left between the MLS remnant and N-terminus of the protein of interest.
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In our characterization, the CDS of MLS was assembled in frame with that of GFP reporter using Freiburg’s RFC25 format. The translation unit was driven by CMV promoter () and terminated by hGH polyA signal ().
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The MLS-GFP generator (BBa_K1119009) was then transfected into HEK293FT cells. Mitochondria were stained after transfection and co-localization was determined by area of signal that overlapped.
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To provide a positive control, CDS of EGFP from pEGFP-N1 (Clontech) was inserted downstream and in frame with the CDS of the MLS in the commercial plasmid pCMV/myc/mito, (Invitrogen, Carlsbard, CA). A negative control was made by GFP generator that does not contains the CDS of MLS (BBa_K1119008).
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The detailed protocol of our characterization can be found in HKUST iGEM 2013 Wiki.
  
 
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Revision as of 05:00, 26 September 2013

Mitochondrial Leader Sequence in RFC10 standard

Mitochondrial Leader Sequence (MLS) helps direct protein to the mitochondria when this peptide sequence is in front of the N-terminus of the protein of interest. MLS will be removed upon the peptide’s translocation into the mitochondria, but four additional amino acid residues (Ile-His-Ser-Leu) will be left at the N-terminus of the protein. (Invitrogen, Carlsbard, CA) Under the RFC25 standard, two additional amino residue linker (Ala-Gly) will be left between the MLS remnant and N-terminus of the protein of interest.


In our characterization, the CDS of MLS was assembled in frame with that of GFP reporter using Freiburg’s RFC25 format. The translation unit was driven by CMV promoter () and terminated by hGH polyA signal (). The MLS-GFP generator (BBa_K1119009) was then transfected into HEK293FT cells. Mitochondria were stained after transfection and co-localization was determined by area of signal that overlapped. To provide a positive control, CDS of EGFP from pEGFP-N1 (Clontech) was inserted downstream and in frame with the CDS of the MLS in the commercial plasmid pCMV/myc/mito, (Invitrogen, Carlsbard, CA). A negative control was made by GFP generator that does not contains the CDS of MLS (BBa_K1119008). The detailed protocol of our characterization can be found in HKUST iGEM 2013 Wiki.

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]