Difference between revisions of "Part:BBa K3504009"
Ahmed Wael (Talk | contribs) |
Ahmed Wael (Talk | contribs) (→Characterization) |
||
Line 8: | Line 8: | ||
==Usage== | ==Usage== | ||
==Characterization== | ==Characterization== | ||
+ | [[Image:MutationChar1.PNG|thumb|left|Figure 1.Method for in vitro replicon evolution: Jurkat cells were transfected with replicon RNA encoding mCherry under the SGP and grown in cell culture. The top 20% of the mCherry+ population were sorted for approximately every 10 days during serial passaging as indicated by the flow cytometry histograms, leading to an enrichment in cells expressing high levels of the reporter gene. Cells from the 5th sort were isolated for replicon sequencing.]] | ||
+ | |||
+ | [[Image:MutationChar2.PNG|thumb|right|Figure 2.Identification of mutations: Total RNA from mCherry positive cells was extracted and reverse transcribed to cDNA. Then, nsP1–4 and the subgenomic promoter were amplified by seven pairs of specific primers and amplicons from Loci 1–7 were engineered into plasmid DNA and transformed into E. coli for amplication. Six clones from each locus were randomly picked for Sanger Sequencing. Schematic at bottom left shows the approximate locations in nsP2 and nsP3 where point mutations were identified in 5 mutant alleles with c2 harboring two linked mutations.]] | ||
+ | <br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /><br /> | ||
+ | |||
==Improvements== | ==Improvements== | ||
Using information in literature we were able to increase the replicon cloning and functional ability by adding G110G, G763R Mutation to NSP2 and adding K94E, S243G,E255D,V305M Mutation to NSP3 | Using information in literature we were able to increase the replicon cloning and functional ability by adding G110G, G763R Mutation to NSP2 and adding K94E, S243G,E255D,V305M Mutation to NSP3 |
Revision as of 08:46, 13 October 2020
Alphavirus replicon NSPs- Equine Encephalitis virus
Part Description
A composite of parts (BBa_K3504000,BBa_K3504001,BBa_K3504002,BBa_K3504003) and CMV promoter which form ,as a unit, the main constituent of alphavirus replicon which as a whole can give the circuit self-replicating ability
Usage
Characterization
Improvements
Using information in literature we were able to increase the replicon cloning and functional ability by adding G110G, G763R Mutation to NSP2 and adding K94E, S243G,E255D,V305M Mutation to NSP3
References
Li, Y., Teague, B., Zhang, Y., Su, Z., Porter, E., Dobosh, B., ... & Weiss, R. (2019). In vitro evolution of enhanced RNA replicons for immunotherapy. Scientific reports, 9(1), 1-10. Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 2760
Illegal SpeI site found at 2708
Illegal PstI site found at 5089 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 2760
Illegal NheI site found at 5960
Illegal NheI site found at 7290
Illegal NheI site found at 8107
Illegal SpeI site found at 2708
Illegal PstI site found at 5089 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 2760
Illegal BglII site found at 2882
Illegal BamHI site found at 2744
Illegal BamHI site found at 3107
Illegal XhoI site found at 6124
Illegal XhoI site found at 6185
Illegal XhoI site found at 6226 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 2760
Illegal SpeI site found at 2708
Illegal PstI site found at 5089 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 2760
Illegal SpeI site found at 2708
Illegal PstI site found at 5089
Illegal NgoMIV site found at 3549
Illegal AgeI site found at 5665
Illegal AgeI site found at 6034
Illegal AgeI site found at 6361 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1635
Illegal BsaI site found at 6223
Illegal BsaI site found at 6241
Illegal BsaI.rc site found at 3012
Illegal BsaI.rc site found at 3659
Illegal BsaI.rc site found at 5750