Difference between revisions of "Part:BBa K192000"
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The 2018 EPFL iGEM team has improved upon this part by using a different sequence derived from a plasmid used in David Savage's lab (Cassidy-Armstutz et al., 2016). Additionally the team introduced a HexaHistidine loop (GGGGGGHHHHHHGGGGG) into the protein's sequence to improve the heat resistance and to provide better hydrodynamic properties (Moon et al., 2014). | The 2018 EPFL iGEM team has improved upon this part by using a different sequence derived from a plasmid used in David Savage's lab (Cassidy-Armstutz et al., 2016). Additionally the team introduced a HexaHistidine loop (GGGGGGHHHHHHGGGGG) into the protein's sequence to improve the heat resistance and to provide better hydrodynamic properties (Moon et al., 2014). | ||
The composite part [[parts.igem.org/Parts:BBa_K2686005|BBa_K2686005]] encodes this modified Encapsulin sequence and presents an upgrade due to BsaI cut sites and sfGFP under a native promoter which allow for the rapid introduction of antigen encoding sequences to the Encapsulin monomer's C terminus. | The composite part [[parts.igem.org/Parts:BBa_K2686005|BBa_K2686005]] encodes this modified Encapsulin sequence and presents an upgrade due to BsaI cut sites and sfGFP under a native promoter which allow for the rapid introduction of antigen encoding sequences to the Encapsulin monomer's C terminus. | ||
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| + | [[File:IGEM Encap.png|thumb|center|upright=3|bleep]] | ||
Revision as of 07:24, 17 October 2018
Encapsulin
Toronto 2009
BBa_K192000 is a shell-forming protein known as "encapsulin", which we derived from the TM0785 plasmid in T. maritima. The protein is a monomer which assembles into a thin icosahedral shell with a diameter of 240 angstroms resulting in a nanocompartment lined with conserved binding sites for short polypeptide tags present as C-terminal extensions of enzymes. In T. maritima, these enzymes are involved in oxidative-stress response. We have isolated the encapsulin gene in E. coli, in which we plan to characterize as an expression system for the application of channeling candidate enzyme pairs identified in silico.
Improvement from iGEM EPFL 2018
The 2018 EPFL iGEM team has improved upon this part by using a different sequence derived from a plasmid used in David Savage's lab (Cassidy-Armstutz et al., 2016). Additionally the team introduced a HexaHistidine loop (GGGGGGHHHHHHGGGGG) into the protein's sequence to improve the heat resistance and to provide better hydrodynamic properties (Moon et al., 2014). The composite part BBa_K2686005 encodes this modified Encapsulin sequence and presents an upgrade due to BsaI cut sites and sfGFP under a native promoter which allow for the rapid introduction of antigen encoding sequences to the Encapsulin monomer's C terminus.
