Difference between revisions of "Part:BBa K1442040"
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+ | The MS2 protein binding box is a highly specific RNA hairpin loop structure in viral RNA that binds the MS2 coat protein of the bacteriophage in order to allow encapsidation of the genome and represses the translational of replicase synthase [1]. Exploiting the MS2 box-protein binding relationship is known as MS2 tagging <p> </p> | ||
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+ | Isaacs et al [2] noted that the MS2 protein binding box is of use for engineering RNA transcriptional activators via the DNA-protein binding interactions and the hairpin has thus been shown that the MS2 box can be used to drive expression of proteins when localised to a promoter (e.g. the MS2 protein is fused to a DNA-binding protein and the MS2 box is localised to its target promoter, driving expression). <p></p> | ||
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+ | Furthermore, Auslander et al [3] also showed that the MS2 protein-box relationship can be designed for use in synthetic biology to create programmable single-cell mammalian biocomputers with simple expression logic, increasing the complexity of a informational processing system without researcher input. | ||
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Revision as of 19:20, 16 October 2014
MS2 bacteriophage coat protein
Isaacs et al [2] noted that the MS2 protein binding box is of use for engineering RNA transcriptional activators via the DNA-protein binding interactions and the hairpin has thus been shown that the MS2 box can be used to drive expression of proteins when localised to a promoter (e.g. the MS2 protein is fused to a DNA-binding protein and the MS2 box is localised to its target promoter, driving expression).
Furthermore, Auslander et al [3] also showed that the MS2 protein-box relationship can be designed for use in synthetic biology to create programmable single-cell mammalian biocomputers with simple expression logic, increasing the complexity of a informational processing system without researcher input.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 255
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 255
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 255
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 255
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 255
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 292