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< Prokaryotic Expression >. trc Expression System ( pTrcHis TOPO TA Expression System ) 약학대학 2005-30580 조승주. Prokaryotic Expression Systems. -Invitrogen-. trc Expression System. trc promoter → The trc promoter, a hybrid promoter containing the -35 region from the
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< Prokaryotic Expression > trc Expression System (pTrcHis TOPO TA Expression System) 약학대학 2005-30580 조승주
Prokaryotic Expression Systems -Invitrogen-
trc Expression System trc promoter → The trc promoter, a hybrid promoter containing the -35 region from the trpB promoter and the -10 region from the lacUV5 promoter for high-level expression in E. coli. → Inducible promoter → Repressed by the lac repressor (lacI) → Chemically induced with iospropyl-β-D-thiogalactopyranoside (IPTG)
Description of the Vectors → The trc promoter → The lacO sequence for binding the Lac repressor encoded by the lacIq gene. In the absence of IPTG, Lac repressor binds to the lacO sequence, repressing transcription. Upon addition of IPTG, expression is induced. → rrnB antitermination sequence the reduces premature transcription termination. → T7 gene 10 translational enhancer sequence for more efficient translational initiation. → A minicistron containing nucleotides that are efficiently translated in prokaryotic cells for enhanced translational efficiency. → Xpress epitope is part of the bacteriophage T7 gene 10 protein
TOPO Cloning → Single 3’-thymidine (T) overhangs for TA Cloning → Topoisomerase I covlently bound to the vector (this is referred to as “activated” vector)
pTrcHis-TOPO TA Expression → Efficient cloning of PCR products into a prokaryotic expression vector for high-level → Regulated expression from the trc promoter → Minicistron element for enhanced translation efficiency of eukaryotic proteins in E. coli. → Provided linearized and activated with topoisomerase I for 5-minute TOPO Cloning with >85% cloning efficiency → Symplify protein purification and detection N-terminal Xpress epitope for detection with an Anti-Xpress Antibody N-terminal polyhistidine (6xHis) tag for purification using nickel-chelating resin and detection with an Anti-HisG Antibody Enterokinase cleavage site for efficient removal of N-terminal fusion tags