Refolding Record:
Protein | |
---|---|
Protein Name | Beta-2-microglobulin |
Abbreviated Name | Beta2m |
SCOP Family | C1 set domains (antibody constant domain-like) |
Structure Notes | |
Organism | Human |
UniProt Accession | P61769 |
SCOP Unique ID | n/a |
Structure Solved | |
Class | Beta |
Molecularity | Monomer |
Construct | |
---|---|
Full Length | y |
Domain | n/a |
Chimera | n/a |
Variants | n/a |
Chain Length | 99 |
Molecular Weight | 11731.2 |
Pi | 6.07 |
Molecular Weight | 11731.2 |
Disulphides | 1 |
Full Sequence |
IQRTPKIQVY SRHPAENGKS NFLNCYVSGF HPSDIEVDLL KNGERIEKVE HSDLSFSKDW SFYLLYYTEF TPTEKDEYAC RVNHVTLSQP KIVKWDRDM
|
Notes | n/a |
Expression | |
---|---|
Report | Garboczi DN, Hung DT, Wiley CD (1992) Proc. Natl. Acad. Sci. USA, 89, 3429-3433 |
Project Aim | Crystallography |
Fusion | None |
Protein Expression and Production | Protein recombinantly expressed as and refolded from inclusion bodies. |
Expression Host | Escherichia coli |
Expression Strain | XA90 |
Expression Temp | 37.0 |
Expression Time | 4h |
Expression Vector | pHN1+ |
Expression Protocol | 400ml of LB medium was inoculated with 100ml stationary phase culture and grown at 37degC. After 30min incubation, 0.5mM IPTG was added and the cells were incubated a further 4h. Cells were collected by centrifugation and the inclusion bodies were isolated. |
Method of Induction | IPTG |
Cell Density at Induction | OD = |
Cell Disruption Method | Sonication |
Lytic Agent | None |
Pre-Refolding Purification | None |
Solubility | insoluble |
Refolding | |
---|---|
Refolding Method | Dilution with complex partner subunits |
Wash Buffer | n/a |
Solubilization Buffer | 8M urea, 50mM 2-(N-morpholino)ethansulfonic acid pH 6.5, 0.1mM EDTA, 0.1mM DTT |
Refolding Buffer | 100mM TrisHCl pH 8, 400mM L-arginineHCL, 2mM EDTA, 5mM reduced glutathione, 0.5mM oxidized glutathione, 0.5mM PMSF |
Pre-Refolding Purification | None |
Tag Cleaved | yes |
Refolding pH | 8.0 |
Refolding Temperature | 10.0 |
Protein Concentration | 2microM |
Refolding Time | 24-36h |
Redox Agent | GSH/GSSG |
Redox Agent Concentration | 5mM/0.5mM |
Refolding Protocol | The inclusion body pellet was dissolved in 10ml solubilization buffer and then centrifuged (150000g). Refolding was initiated by dilution with denatured class I histocompatibility antigen HLA-A2 and an antigenic peptide into 200ml refolding buffer. Final protein concentrations were 1microM HLA-A2, 2microM beta-2-microglobulin, 10microM peptide. The refolding mixture was incubated at 10degC for 24-36h. The refolding mixture was concentrated and then subjected to gel filtration HPLC. |
Refolding Assay | HPLC |
Refolding Chaperones | None |
Refolding Additives | None,L-Arginine |
Additives Concentration | 400mM |
Refolding Yield | |
Purity | |
Notes |