Difference between revisions of "Part:BBa K3016100"
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<partinfo>BBa_K3016100 short</partinfo> | <partinfo>BBa_K3016100 short</partinfo> | ||
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This part contains <i>Vibrio natriegens'</i> TorA Tat signal peptide. It is a twin-arginine (RR) motif containing signal peptide for periplasmic transport of proteins via the twin-arginine translocation (Tat) pathway. Derived from Vibrio natriegens’ <i>torA gene</i>. | This part contains <i>Vibrio natriegens'</i> TorA Tat signal peptide. It is a twin-arginine (RR) motif containing signal peptide for periplasmic transport of proteins via the twin-arginine translocation (Tat) pathway. Derived from Vibrio natriegens’ <i>torA gene</i>. | ||
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This part can be N-terminally fused with your protein of choice to facilitate its periplasmic transport via the twin-arginine translocation (Tat) pathway. | This part can be N-terminally fused with your protein of choice to facilitate its periplasmic transport via the twin-arginine translocation (Tat) pathway. | ||
− | Aalto-Helsinki 2019 used this part by combining it with YGFP, a slow-bleaching GFP variant, creating a composite TorA-YGFP part ([ ]) to test protein translocation into <i>Vibrio natriegens'</i> and <i>Escherichia coli's</i> periplasm. | + | Aalto-Helsinki 2019 used this part by combining it with YGFP ([https://parts.igem.org/Part:BBa_K3016600 BBa_K3016600]), a slow-bleaching GFP variant, creating a composite TorA-YGFP part ([https://parts.igem.org/Part:BBa_K3016200 BBa_K3016200]) to test protein translocation into <i>Vibrio natriegens'</i> and <i>Escherichia coli's</i> periplasm. |
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Revision as of 20:45, 20 October 2019
Vibrio natriegens' TorA signal peptide
This part contains Vibrio natriegens' TorA Tat signal peptide. It is a twin-arginine (RR) motif containing signal peptide for periplasmic transport of proteins via the twin-arginine translocation (Tat) pathway. Derived from Vibrio natriegens’ torA gene.
Biology
The twin-arginine translocation (Tat) pathway is capable of translocating fully folded proteins up to 150 kDa. It also contains a quality control feature of rejecting misfolded proteins. In some cases, disulfide bridge formation is not required for successful translocation. (Alanen et al., 2015)
Translocation using the tat-pathway requires the protein to contain a N-terminal signal peptide with a twin-arginine (RR) motif. The signal peptide is cleaved during the translocation process. A pair of V. natriegens’ native twin-arginine signal peptides identified by Aalto-Helsinki can be found here (TorAand Aminotransferase)
Use
This part can be N-terminally fused with your protein of choice to facilitate its periplasmic transport via the twin-arginine translocation (Tat) pathway.
Aalto-Helsinki 2019 used this part by combining it with YGFP (BBa_K3016600), a slow-bleaching GFP variant, creating a composite TorA-YGFP part (BBa_K3016200) to test protein translocation into Vibrio natriegens' and Escherichia coli's periplasm.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]