Difference between revisions of "Part:BBa K2065002:Experience"

Revision as of 00:01, 19 October 2016

Applications of BBa_K2065002

iGEM TU Eindhoven 2016

iGEM TU Eindhoven created this scaffold protein by computational design and checked its functioning and orthogonality using the NanoBiT reporter system. This system was linked to CT52 (CT52-SmallBiT"https://parts.igem.org/Part:BBa_K2065000" and CT52-LargeBiT"https://parts.igem.org/Part:BBa_K2065007") These two proteins could dimerize on our heterodimeric T-14-3-3 scaffold proteins with mutation which were designed by our team. When dimerized the functional luciferase protein was formed. This protein showed luminescence at 460 nm. Thus this system was used as a read out method for T14-3-3 heterodimers. This system is schemtically visualised in figure 1. For more detailed information about the application of CT52-SmallBiT visit our wiki.

Figure 1: Measurement system for T14-3-3 heterodimers using the NanoBiT system linked to CT52

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UNIQead1fc538677fa78-partinfo-00000000-QINU UNIQead1fc538677fa78-partinfo-00000001-QINU

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 ==iGEM TU Eindhoven 2016==
-iGEM TU Eindhoven created this scaffold protein by computational design and checked its functioning and orthogonality using the NanoBiT reporter system. This was accomplished by linking CT52, the protein which has affinity to the T14-3-3 and complementary mutant form to parts of this reporter system
+iGEM TU Eindhoven created this scaffold protein by computational design and checked its functioning and orthogonality using the NanoBiT reporter system. This system was linked to CT52 (CT52-SmallBiT"https://parts.igem.org/Part:BBa_K2065000" and CT52-LargeBiT"https://parts.igem.org/Part:BBa_K2065007") These two proteins could dimerize on our heterodimeric T-14-3-3 scaffold proteins with mutation which were designed by our team. When dimerized the functional luciferase protein was formed. This protein showed luminescence at 460 nm. Thus this system was used as a read out method for T14-3-3 heterodimers. This system is schemtically visualised in figure 1. For more detailed information about the application of CT52-SmallBiT visit our wiki.
-iGEM TU Eindhoven used this part in combination with the NanoBiT system linked to CT52(CT52-SmallBiT"https://parts.igem.org/Part:BBa_K2065000" and CT52-LargeBiT"https://parts.igem.org/Part:BBa_K2065007" These two proteins could dimerize on our heterodimeric T-14-3-3 scaffold proteins with mutation which were designed by our team. When dimerized the functional luciferase protein was formed. This protein showed luminescence at 460 nm. Thus this system was used as a read out method for T14-3-3 heterodimers. This system is schemtically visualised in figure 1. For more detailed information about the application of CT52-SmallBiT visit our wiki.
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