Difference between revisions of "Part:BBa K3866013"

(Verification of Cloning)
(Verification of Cloning)
 
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===Verification of Cloning===
 
===Verification of Cloning===
[[File:T--Thessaly--BLgel.png|700px|thumb|none|<i><b>Fig.2:</b>: (U=Uncut , C= Cut)Positive clone 7: omega 2 BARR-eCFP. Expected bands 2900, 2214, 1241, 832</i>]]
+
[[File:T--Thessaly--BLgel.png|700px|thumb|none|<i><b>Fig.2:</b>: (U=Uncut , C= Cut)Positive clone 8: omega 2 BARR-eCFP. Expected bands 2900, 2214, 1241, 832</i>]]
  
 
===Experimental Use and Experience===
 
===Experimental Use and Experience===

Latest revision as of 13:55, 4 October 2021


ParaBAD:RBS- β-arrestin2:TEVp:terminator---pAndersonJ23115:lacO:RBS-eCFP -terminator


Usage and Biology

This part has an inducible promoter from arabinose, leading to a regulated expression of the transcription unit. B-arrestin has the ability to normally bind to the GPCR receptor and facilitate its endocytosis, desensitization or GPCR-independent signaling effects. The second composite of our TANGO system is a fusion of the b-arrestin-2 with the TEV protease.TEV protease recognizes and cleaves the cleavage site. This low proximity allows the TEV protease that is tagged to the βarrestin-2 carrier to cleave its substrate (TCS) .

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 seva omega2 vector BBa_K3505011and has overhangs compatible for GoldenBraid cloning.


Figure 1. The level Ω module of GPCR-Tango module : B-arrestin -TEV protease- ECFP

Verification of Cloning

Fig.2:: (U=Uncut , C= Cut)Positive clone 8: omega 2 BARR-eCFP. Expected bands 2900, 2214, 1241, 832

Experimental Use and Experience

This part was used in BBa_K3866014


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 2854
    Illegal PstI site found at 1546
    Illegal PstI site found at 1633
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 3358
    Illegal NheI site found at 3381
    Illegal SpeI site found at 2854
    Illegal PstI site found at 1546
    Illegal PstI site found at 1633
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1446
    Illegal BamHI site found at 1148
    Illegal XhoI site found at 1843
    Illegal XhoI site found at 2237
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 2854
    Illegal PstI site found at 1546
    Illegal PstI site found at 1633
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal SpeI site found at 2854
    Illegal PstI site found at 1546
    Illegal PstI site found at 1633
    Illegal AgeI site found at 983
    Illegal AgeI site found at 1829
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 965
    Illegal SapI.rc site found at 2788
    Illegal SapI.rc site found at 3136