= SGC clone accession =
JMC061-H05
= Tag =
N-terminal His6-tag,
= Construct comments =
= Construct sequence =
MHHHHHHSSGRENLYFQGTAPQPEQCMFHDDWISSIKGAEEWILTGSYDKTSRIWSLEGKSIMTIVGHTDVVKDVAWVKK
DSLSCLLLSASMDQTILLWEWNVERNKVKALHCCRGHAGSVDSIAVDGSGTKFCSGSWDKMLKIWSTVPTDEEDEMEEST
NRPRKKQKTEQLGLTRTPIVTLSGHMEAVSSVLWSDAEEICSASWDHTIRVWDVGSGSLKSTLTGNKVFNCISYSPLCKR
LASGSTDRHIRLWDPRTKDGSLVSLSLTSHTGWVTSVKWSPTHEQQLISGSLDNIVKLWDTRSCKAPLYDLAAHEDKVLS
VDWTDTGLLLSGGADNKLYSYRYSPTTSHVG
DNA sequence has been verified by sequencing
= Vector =
pFBOH-MHL
= Expression host =
Spodoptera frugiperda
= Growth method =
Shaker
The recombinant donor vector pFBOH-MHL: WDR12 was transformed into DH10Bac E. coli cells (Invitrogen) to generate recombinant viral DNA.
Sf9 cells (Invitrogen) were transfected with Bacmid DNA using jetPRIME® transfection reagent (PolyPlus Transfection), and recombinant baculovirus particles were recovered.
The recombinant virus sequentially amplified from P1 to P3 viral stocks. Sf9 cells grown in I-Max Insect medium (Wisent Biocenter, Cat.# 301-045-LL) to a density of 4mln/mL and with viability not less than 97% were infected with 10 mL of P3 viral stock for each 1 L of cell culture.
Cultured cells were collected when cell viability dropped to 75-80%, normally after 4 days of post-infection time
= Extraction buffers =
20mM Tris pH8.0, 500 mM NaCl with 5% glycerol
= Extraction procedure =
Native cell pellet was resuspended in extraction buffer and the cells disrupted by sonication for
10 mins at 5" on 10" off duty cycle at 90W output power.
= Purification buffers =
loading buffer: 20mM Tris pH8.0, 500 mM NaCl with 5% glycerol
Washing Buffer: 20mM Tris pH8.0, 500 mM NaCl with 5% glycerol, 5 mM imidazole
Elution Buffer: 20mM Tris pH8.0, 500 mM NaCl with 5% glycerol, 250 mM imidazole
= Purification procedure =
The crude extract was cleared by centrifugation. The lysate was loaded onto 1ml (1ml/L)Talon Metal Affinity Resin (Cat# 635504 Clontech).
The resin was washed with 50 CV of loading buffer (20mM Tris pH8.0, 500 mM NaCl with 5% glycerol) and 5 CV loading buffer with 5mM imidazole.
The protein was eluted with elution buffer (loading buffer with 250 imidazole). The protein was further purified by Superdex200 (GE Healthcare) using 20 mM Tris pH8.0 plus 150 mM NaCl. His tag was removed overnight at 4oC.
The third purification step was the Source Q using 20mM Tris pH7.5(buffer A)with 1M NaCl (buffer B).
Purification yield was 2.5 mg of the protein per 1L of culture.
= Protein stock concentration =
Concentration used for crystallization : 10.0 mg/mL
= Mass spec =
--
= Functional multimerization =
Monomer
= Crystallization =
Crystallization of 6N31 was performed in 96 well vapor diffusion sitting drop plates by mixing equal volumes of protein and reservoir solution at 20°C.
Diffracting quality crystals were grown in 25% PEG 3350, 0.2M magnesium chloride, 0.1M Hepes 7.5.
Crystals were cryoprotected in reservoir solution supplemented with 20% (v/v) Glycerol and cryocooled in liquid nitrogen.
