Difference between revisions of "Part:BBa K3505025"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | This composite part constitutes the G-protein coupled bioreceptor composite of the dual TANGO-GPCR assay (the other part is the b-arrestin-2 constituent, placed under the control of the arabinosed-induced promoter. FFAR2 is a naturally found eukaryotic GPCR protein that exhibits high affinity for SCFAs (acetic, propionic and butyric acid). After background searching through the NCBI database, we have identified the gene coding sequences needed for the designing of this gene construct. More specifically, a vasopressin receptor 2 segment has been attached to the C-terminal of the receptor, as it mediates recruitment of a TEV tagged b-arrestin-2, along with a TEV cleavage site | + | This composite part constitutes the G-protein coupled bioreceptor composite of the dual TANGO-GPCR assay (the other part is the b-arrestin-2 constituent, placed under the control of the arabinosed-induced promoter. FFAR2 is a naturally found eukaryotic GPCR protein that exhibits high affinity for SCFAs (acetic, propionic and butyric acid). After background searching through the NCBI database, we have identified the gene coding sequences needed for the designing of this gene construct. More specifically, a vasopressin receptor 2 segment has been attached to the C-terminal of the receptor, as it mediates recruitment of a TEV tagged b-arrestin-2, along with a TEV cleavage site. |
Sequence and Features | Sequence and Features | ||
Revision as of 18:51, 27 October 2020
ParaBAD:RBS-FFAR2:AVPR2 tail:TCS-LacI-terminator
Usage and Biology
This composite part constitutes the G-protein coupled bioreceptor composite of the dual TANGO-GPCR assay (the other part is the b-arrestin-2 constituent, placed under the control of the arabinosed-induced promoter. FFAR2 is a naturally found eukaryotic GPCR protein that exhibits high affinity for SCFAs (acetic, propionic and butyric acid). After background searching through the NCBI database, we have identified the gene coding sequences needed for the designing of this gene construct. More specifically, a vasopressin receptor 2 segment has been attached to the C-terminal of the receptor, as it mediates recruitment of a TEV tagged b-arrestin-2, along with a TEV cleavage site. Sequence and Features
Design Notes
The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in alpha1R vector BBa_K3505008 and has overhangs compatible for Golden Braid cloning.
Verification of Cloning
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 1527
Illegal PstI site found at 2107 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 1527
Illegal PstI site found at 2107 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1148
Illegal BamHI site found at 1349 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 1527
Illegal PstI site found at 2107 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 1527
Illegal PstI site found at 2107
Illegal NgoMIV site found at 1607
Illegal AgeI site found at 983 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 965
Illegal SapI site found at 1803
Illegal SapI site found at 2058
Illegal SapI.rc site found at 1260