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[[IGEM:Hong_Kong_HKUST | <font face="trebuchet ms" style="color:#ffffff"> '''Home''' </font>]] &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
[[IGEM:Hong_Kong_HKUST | <font face="trebuchet ms" style="color:#ffffff"> '''Home''' </font>]] &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
[[IGEM:Hong_Kong_HKUST/Investigations | <font face="trebuchet ms" style="color:#ffffff"> '''Investigations''' </font>]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[[IGEM:Hong_Kong_HKUST/Parts_clipping | <font face="trebuchet ms" style="color:#ffffff"> '''Parts Clipping''' </font>]] &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
[[IGEM:Hong_Kong_HKUST/Investigations | <font face="trebuchet ms" style="color:#ffffff"> '''Investigations''' </font>]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[[IGEM:Hong_Kong_HKUST/Parts_clipping | <font face="trebuchet ms" style="color:#ffffff"> '''Parts Clipping''' </font>]] &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
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<h1>Parts Clipping</h1>


Parts Clipping
Reading through wikis, we may come across parts that we find interesting and potentially helpful in building the next iGEM project. Similar to newspaper clipping, here we write short descriptions of BioBricks and post them up here as an exercise.


Reading through wikis, we may come across parts that we find interesting and potentially helpful in building the next iGEM project. Here we write short descriptions of BioBricks and post them up here as an exercise.
<br>


Entry by *'''[[User:Trevor Y. H. Ho|Trevor Y. H. Ho]] 22:51, 29 January 2015 (EST)'''
<h1>Entries</h1>
Cohort: 2011 HKUST iGEM
<br>
Part: BBa_
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<h3>P2A peptide [http://parts.igem.org/Part:BBa_K1442039 BBa_K1442039]</h3>
*'''[[User:Trevor Y. H. Ho|Trevor Y. H. Ho]] 08:05, 17 February 2015 (EST)'''


<ul>
<li><b>Training cohort:</b> 2015 HKUST iGEM</li>
<li>
<b>Part Description:</b>
<br>
The P2A peptide sequence is a stretch of amino acid residues (A T N F S L L K Q A G D V E E N P G P) that allows monocistronic mammalian genes to be polycistronic. During mammlian translation, the ribosome running through the codons containing this peptide "skips" the formation of amide bond between the glycine and the proline residue at the C terminus but continue translation on the codons that follow afterwards. As such, it creates an invisible stop codon after the glycine residue and makes the following proline the new <i>de facto</i> start codon. Therefore the peptide is essentially split into half and thus this peptide bears a misnomer as a “self-cleaving” peptide.
</li>
<li>
<b>Comments:</b>
<br>
The P2A peptide has been known to provide a good alternative to internal ribosomal entry site (IRES), but what it interested me is: the mechanism of action essentially locks the production rates of translation in an equal molar ratio. That would be especially helpful for efficient production of heterodimers / heterocomplexes.
<br>
</li>
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[[Category:Lab]]
[[Category:Lab]]

Latest revision as of 07:16, 17 February 2015

Home        Investigations        Parts Clipping       


Parts Clipping

Reading through wikis, we may come across parts that we find interesting and potentially helpful in building the next iGEM project. Similar to newspaper clipping, here we write short descriptions of BioBricks and post them up here as an exercise.


Entries

P2A peptide BBa_K1442039

  • Training cohort: 2015 HKUST iGEM
  • Part Description:
    The P2A peptide sequence is a stretch of amino acid residues (A T N F S L L K Q A G D V E E N P G P) that allows monocistronic mammalian genes to be polycistronic. During mammlian translation, the ribosome running through the codons containing this peptide "skips" the formation of amide bond between the glycine and the proline residue at the C terminus but continue translation on the codons that follow afterwards. As such, it creates an invisible stop codon after the glycine residue and makes the following proline the new de facto start codon. Therefore the peptide is essentially split into half and thus this peptide bears a misnomer as a “self-cleaving” peptide.
  • Comments:
    The P2A peptide has been known to provide a good alternative to internal ribosomal entry site (IRES), but what it interested me is: the mechanism of action essentially locks the production rates of translation in an equal molar ratio. That would be especially helpful for efficient production of heterodimers / heterocomplexes.