Refolding Record:
Protein | |
---|---|
Protein Name | Beta 1, 4 galactosyltransferase I |
Abbreviated Name | B4(Gal-T1) |
SCOP Family | beta 1,4 galactosyltransferase (b4GalT1) |
Structure Notes | |
Organism | Human |
UniProt Accession | P15291 |
SCOP Unique ID | n/a |
Structure Solved | |
Class | Alpha/Beta |
Molecularity | Dimer |
Construct | |
---|---|
Full Length | y |
Domain | n/a |
Chimera | n/a |
Variants | n/a |
Chain Length | 367 |
Molecular Weight | 40589.2 |
Pi | 8.72 |
Molecular Weight | 40589.2 |
Disulphides | 2 |
Full Sequence |
MASMTGGQQMGRGRDLSRLPQLVGVSTPLQGGSNSAAAIGQSSGELRTGGARPPPPLGASSQPRPGGDSSPVVDSGPGPASNLTSVPVPHTTALSLPACPEESPLLVGPMLIEFNMPVDLELVAKQNPNVKMGGRYAPRDCVSPHKVAIIIPFRNRQEHLKYWLYYLHPVLQRQQLDYGIYVINQAGDTIFNRAKLLNVGFQEALKDYDYTCFVFSDVDLIPMNDHNAYRCFSQPRHISVAMDKFGFSLPYVQYFGGVSALSKQQFLTINGFPNNYWGWGGEDDDIFNRLVFRGMSISRPNAVVGRCRMIRHSRDKKNEPNPQRFDRIAHTKETMLSDGLNSLTYQVLDVQRYPLYTQITVDIGTPS
|
Notes | n/a |
Expression | |
---|---|
Report | Boeggeman, E. E., Ramakrishnan, B., Qasba, P. K. (2003) Protein Expression and Purification, 30, 219-229 |
Project Aim | Folding |
Fusion | N-terminal T7 tag |
Protein Expression and Production | Protein recombinantly expressed as and refolded from inclusion bodies. |
Expression Host | Escherichia coli |
Expression Strain | BL21(DE3)pLysS |
Expression Temp | 37.0 |
Expression Time | 3-4h |
Expression Vector | pET-23a |
Expression Protocol | Cells were grown in LB broth containing 50microg/ml ampicillin. Following induction and incubation, cells were harvested by centrifugation (2000g, 20min) and inclusion bodies isolated |
Method of Induction | IPTG |
Cell Density at Induction | OD 600 = 0.7 |
Cell Disruption Method | Not stated |
Lytic Agent | None |
Pre-Refolding Purification | None |
Solubility | insoluble |
Refolding | |
---|---|
Refolding Method | Dilution/Dialysis combination |
Wash Buffer | n/a |
Solubilization Buffer | 5M guanidine-HCl |
Refolding Buffer | 50 mM TrisHCl, pH 8.0, 10.58 mM NaCl, 0.44 mM KCl, 2.2 mM MgCl2, 2.2 mM CaCl2, 0.5 M guanidine-HCl, 8 mM cysteamine, 4 mM cystamine, 0.055% PEG-4000, 0.55M L-arginine |
Pre-Refolding Purification | None |
Tag Cleaved | no |
Refolding pH | 8.0 |
Refolding Temperature | 4.0 |
Protein Concentration | 48h |
Refolding Time | n/a |
Redox Agent | cysteamine/cystamine |
Redox Agent Concentration | 8 mM/ 4 mM respectively |
Refolding Protocol | Inclusion bodies were sulphonated and then dissolved in solubilization buffer to a protein concentration of 1mg/ml, OD600 1.9-2.0. Protein solution was then diluted 10 fold in refolding solution to give a final protein concentration of 100microg/ml. Refolding was allowed to occur for 48h and then solution was dialyzed. |
Refolding Assay | Far-UV Circular Dichroism |
Refolding Chaperones | None |
Refolding Additives | L-Arginine,Polyethylene glycol (PEG) |
Additives Concentration | n/a |
Refolding Yield | n/a |
Purity | n/a |
Notes | n/a |