Expression and Purification of the GRAS Domain of Os-SCL7 from Rice for Structural Studies

Materials and Reagents

1. Amicon Ultra centrifugal filters, 30 K (Merck Millipore, catalog number: UFC903096 )
   
2. Amicon Ultra centrifugal filters 30,000 MWCO (EMD Millipore, catalog number: UFC803024 )
   
3. Economical biotech dialysis membrane, 14 KD (Sangon Biotech, catalog number: TX0111 )
   
4. Escherichia coli (E. coli) (BL21) (Thermo Fisher Scientific, Invitrogen^TM, catalog number: C6000-03 )
   
5. pET32aM (Novagen, modified from pET32a by inserting a TEV proteasecut site inside the NcoI cleavage site) (Figure 1)
   
6. Rice (NM_001057650, residues 201-578)
   
7. Ampicillin (Sangon Biotech, catalog number: A100741 )
   
8. Isopropyl β-D-1-thiogalactopyranoside (IPTG) (Sangon Biotech, catalog number: A100487 )
   
9. Chelating Sepharose Fast FLow (GE Healthcare, catalog number: 17057502 )
   
10. Nickel(II) sulfate hexahydrate (NiSO₄·6H₂O) (Sangon Biotech, catalog number: A600658 )
    
11. Imidazole (Sangon Biotech, catalog number: A500529 )
    
12. TEV (tabacco etch virus) protease (produced in house) (Fang et al., 2007)
    
13. Tryptone (Oxoid, catalog number: LP0042 )
    
14. Yeast extract (Oxoid, catalog number: LP0021 )
    
15. Sodium chloride (NaCl) (Sangon Biotech, catalog number: A501218 )
    
16. Agar (Oxoid, catalog number: LP0011 )
    
17. Tris-base (Sangon Biotech, catalog number: A100826 )
    
18. Hydrochloric acid (HCl) (Sinopharm Chemical Reagent, catalog number: 7647-01-0 )
    
19. Glycerol (Sangon Biotech, catalog number: A100854 )
    
20. Ethylenediaminetetraacetic acid disodium salt (EDTA) (Sangon Biotech, catalog number: A100105 )
    
21. β-mercaptoethanol (AMRESCO, catalog number: 60-24-2 )
    
22. Tween-20 (Sangon Biotech, catalog number: A100777 )
    
23. Ethanol anhydrous (Sangon Biotech, catalog number: A500737 )
    
24. Phosphoric acid ortho (85%) (Sangon Biotech, catalog number: A502803 )
    
25. Acetic acid (Sangon Biotech, catalog number: A501931 )
    
26. Coomassie Brilliant Blue G-250 (Sangon Biotech, catalog number: A100615 )
    
27. Coomassie Brilliant Blue R-250 (Sangon Biotech, catalog number: A100472 )
    
28. SDS (Sangon Biotech, catalog number: A100227 )
    
29. Isopropanol (Sangon Biotech, catalog number: A507048 )
    
30. LB medium (see Recipes)
    
31. LB-agar plates (see Recipes)
    
32. Lysis buffer (see Recipes)
    
33. Chromatography buffer (see Recipes)
    
34. Coomassie Brilliant Blue G-250 buffer (see Recipes)
    
35. SDS-PAGE staining solution (see Recipes)
    
36. SDS-PAGE destaining solution (see Recipes)
    
    
    Figure 1. The map of pET32aM plasmid
    

Equipment

1. 2 L flask
   
2. Spectrophotometer device (Kebo instrument, model: UV-1100 )
   
3. Sonicator (Scientz, model: IID )
   
4. Refrigerated centrifuge (Eppendorf, model: 5810 R )
   
5. Chromatography system (GE Healthcare, model: INV-907 )
   Note: This product has been discontinued.
   
6. HiLoad 16/600 Superdex 200(GE Healthcare, catalog number: 28-9893-35 )
   
7. Electrophoresis system (Liuyi, model: DYY-6D )
   

Procedure

1. Clone the gene encoding the GRAS domain Os-SCL7 from rice (NM_001057650, residues 201-578) into the modified pET32a vector (pET32aM) (Figure 1).
   
2. Transform the recombinant plasmid (OsSCL7_201-578-pET32aM), which was verified by DNA sequencing, into Escherichia coli strain BL21 (DE3) by heat shock method (Hanahan, 1983) and plate on LB-agar plates containing 100 mg/L ampicillin for 12 h at 37 °C.
   
3. Pick a single colony and culture the E. coli in 10 ml LB medium containing 100 mg/L ampicillin at 37 °C for 5 h. Then transfer 10 ml culture to 1 L fresh LB medium containing 100 mg/L ampicillin (in a 2 L flask) and culture at 37 °C until OD₆₀₀ nm reach 0.4-0.6.
   
4. Cool the cultures to about 16 °C and then induce protein expression with 0.3 mM IPTG for 12-14 h at 16 °C, 180 rpm.
   
5. Harvest the cells by centrifugation at 8,800 x g for 5 min and discard the supernatant, then suspend the cells in 50 ml lysis buffer by vortexing.
   
6. Sonicate the resuspended cells on ice with the power of 380 W for 30 min (ultrasonication is set to 2 sec ‘on’ and 6 sec ‘off’, and repeat this cycle).
   Note: The proteins should always be kept on ice and avoided of high energy produced during the ultrasonicaiton process. Havingan interval time should be better in this process (here the ultrasonication process is set as three times with 10 min for each time and 2 min interval between every two times).
   
7. After sonication, centrifuge the sample at 18,000 x g for 30 min.
   
8. Transfer the supernatant to a new tube, add imidazole into the supernatant to a final concentration of 20 mM and mix it thoroughly. Keep the pellet (containing the cell debris and protein aggregates) on ice before being subjected to SDS-PAGE (step 11).
   Note: Adding a final concentration of 20 mM imidazole into the supernatant can effectively reduce non-specific proteins binding.
   
9. Load the sample onto a nickel-sepharose affinity resin (Chelating sepharose Fast FLow) which was pre-equilibrated with lysis buffer.
   
10. Elute the bound protein with lysis buffers containing a gradient of imidazole (10 mM, 20 mM, 50 mM and 500 mM).
    
11. Subject the eluted protein mixed with loading buffer to SDS-PAGE (Figure 2a). The protein of interest should be between 45 kDa and 66.2 kDa, according to the molecular weight 59 kDa of OsSCL7 GRAS domain fused with TRX and 6His-tag.
    Note: In order to get high purity proteins, it’s better to use a series concentration of imidazole to wash the nonspecific binding proteins and make sure each concentration of imidazole could not nearly elute any protein (see Notes). The target proteins are in the 500 mM imidazole eluent.
    
12. Add TEV protease to the eluted proteins of interest (mTEV:mprotein = 1:10) to remove the TRX and 6His-tag from OsSCL7 GRAS domain. Then transfer the mixture to a dialysis membrane and dialyze it in lysis buffer on a rotator overnight at 4 °C.
    Note: In this step the lysis buffer is used to dialyze imidazole to a low concentration, generally it is lower than 5 mM.
    
13. Load the cleaved protein onto the nickel-sepharose affinity resin again. The target proteins are in the flow through and subsequent 20 mM imidazole eluent. The band of target protein is between 35 and 45 kDa, according to the molecular weight 42 kDa of the OsSCL7 GRAS domain (Figure 2b).
    
14. Then load the sample into a HiLoad 16/600 superdex 200 column pre-equilibrated with 1.2 column volume of chromatography buffer (Figure 3a). The samples of OsSCL7 monomer and dimer were assessed by SDS-PAGE (Figure 3b).
    
15. Pool the fractions containing target protein and concentrate the sample to 5 to 8 mg/ml, measured by Bradford method on spectrophotometer device (Bradford, 1976), with Amicon Ultra centrifugal filters for subsequent crystallization experiment.
    

Data analysis

Figure 2. 15% SDS-PAGE analysis of purified OsSCL7 GRAS domain by nickel-sepharose affinity resin stained with Coomassie Brilliant Blue. a. Lane 1: The aggregates (produced in step 8); Lane 2: The flow (step 8); Lane 3: Eluted with 20 mM imidazole; Lane 4: Eluted with 500 mM imidazole; M: Marker. The arrow indicates the similar MW with the predicted MW (59 kDa) of OsCL7 GRAS domain (41.5 KDa) + Trx-tag (17.5 KDa); b. Lane 1: The flow of the second nickel-sepharose affinity resin purification (produced in step 11, The TRX and 6His-tag were cut off from the OsSCL7 GRAS domain), according to the MW of OsSCL7 GRAS domain, around 42 kDa; Lane 2: Elution with 20 mM imidazole, which also contains the OsSCL7 GRAS domain; M: Marker.


Figure 3. Purification of OsSCL7 GRAS domain by size-exclusion chromatography. a. Size-exclusion chromatography (HiLoad 16/600 superdex 200 column), the dimer and monomerof OsSCL7 GRAS domain appear at 72.26 and 79.68 ml respectively, their corresponding molecular weight are 84 kDa and 42 kDa. b. 15% SDS-PAGE analysis of purified OsSCL7 GRAS domain from fractions of the observed peak in size-exclusion chromatography, showing high purity.

Notes

1. The TEV protease prepared here must be pure enough (more than 90%) and the second nickel-sepharose affinity resin step is important for OsSCL7-GRAS domain purification.
   
2. A pre-experiment was performed to determine the concentration of imidazole would elute the target protein well.
   
3. A series concentration of imidazole are used for washing the nonspecific binding proteins (the highest concentration of imidazole used in this step must be lower than which is for elution of the target protein). And Coomassie Brilliant Blue G-250 buffer (see Recipes) is used to detect no proteins can be washed down any longer by each concentration of imidazole.
   

Recipes

1. LB medium
   10 g/L tryptone
   5 g/L yeast extract
   10 g/L NaCl
   
2. LB-agar plates
   10 g/L tryptone
   5 g/L yeast extract
   10 g/L NaCl
   1.5% agar
   
3. Lysis buffer
   500 mM NaCl
   50 mM Tris-HCl buffer (pH 8.0)
   5% glyceral
   0.2 mM EDTA
   2 mM β-mercaptoethanol
   0.1% Tween-20
   
4. Chromatography buffer
   100 mM NaCl
   25 mM Tris-HCl buffer (pH 8.0)
   5% glycerol
   
5. Coomassie Brilliant Blue G-250 buffer
   47.5 ml ethanol anhydrous
   100 ml phosphoric acid ortho (85%)
   0.1 g G-250
   Add ddH₂O to 1 L
   
6. SDS-PAGE staining solution
   300 ml ethanol anhydrous
   100 ml acetic acid
   1 g Brilliant Blue R-250
   Add ddH₂O to 1 L
   
7. SDS-PAGE destaining solution
   300 ml ethanol anhydrous
   100 ml acetic acid
   Add ddH₂O to 1 L
   

Acknowledgments

This work was supported by the National Natural Science Foundation of China (31500218).

References

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