SGC clone accession TcCLB.506553.20_1-120
Tag removed
Construct sequence gMGKRGREGTLDKARCLAFVHQLWDKDKLKMFHHPISAAELPDYHKVINYPVDLSTIRQGIESGKYDSDADVQNAVAQMIANALEYNAKGTEWHQQALSFRSIYLDVARQCGLSVDDDAAY
Vector pET15-MHL
Expression host BL21(DE3)-pRARE2
Growth medium TB
Growth method Express plasmid in E. coli BL21(DE3)-pRARE2 on LB(Lauria broth) plate in the presence of ampicillin(100mg/ml)+chloramphenicol (34 mg/mL). A single colony was inoculated into 25 mL of TB with ampicillin(100mg/ml)+chloramphenicol (34 mg/mL) in a 50 mL falcon tube and incubated with shaking at 220 rpm overnight at 37 ºC. Then the culture was transfer into 1L of TB with ampicillin(100mg/ml)+chloramphenicol (34 mg/mL), 9ml 0.8M MgSO4, 180ul trace element and 0.5 mL of antifoam (Sigma) in a 1 L bottle and cultured using the LEX system to an
OD600 of ~5, cooled to 15 ºC, and induced with 0.5 mM isopropyl-1-thio-D-galactopyranoside (IPTG) overnight at 15 ºC
Extraction buffers Binding Buffer: 50 mM HEPES pH 7.5, 500 mM NaCl, 5 mM imidazole, and 5 % glycerol
Extraction procedure The culture was harvested by centrifugation. Pellets from 1 L of culture were resuspended to approximately 40 mL/L of cell culture in Binding Buffer with the addition of protease inhibitors (1 mM benzamidine and 1 mM phenylmethyl sulfonyl fluoride (PMSF)). Resuspended pellets stored at -80oC were thawed overnight at 4 °C on the day before purification. Prior to lysis, each pellet from 1 L of culture was pretreated with protease inhibitors, 0.5% CHAPS and 500 units of benzonase. Each liter of cells were sonicated for effective time 5 minutes(about 120 watts, pulsed 10s on, 10s off) and the cell lysate was centrifuged using a Beckman JA-16.25 rotor at 16,000 rpms for an hour at 10 ºC
Purification buffers Wash Buffer: 50 mM HEPES pH 7.5, 500 mM NaCl, 30 mM imidazole, and 5 % glycerol
Elution Buffer: 50 mM HEPES pH 7.5, 500 mM NaCl, 250 mM imidazole, and 5 % glycerol
Gel Filtration buffer: 20mM HEPES 7.5 and 150 mM NaCl.
Purification procedure The cleared lysate was loaded onto a 2 mL Ni-NTA (Qiagen) column pre-equilibrated with Binding Buffer at approximately 1 – 1.5 mL/min. After the lysate was loaded, the column was then washed with at least 200 mL of Wash Buffer. After washing, the protein was eluted with 15 mL of Elution Buffer and treated with 1mM TCEP.
The sample was then loaded onto a superdex 200 gel filtration column. The eluted protein was concentrated using a 15 mL Amicon Ultra centrifugal filter device (Millipore) with a 10 kDa cutoff. The protein was concentrated to 14 mg/mL and flash frozen in N2(l) and stored at -80C.
Protein concentration protein concentration:10 mg/ml in 20mM HEPES7.5 and 150 mM NaCl.
Crystallization The protein was crystallized at 293 K with 0.1 M bTris 5.5, 2M NH4SO4 with 2mM bromosporine using the sitting drop method
