Inclusion Body Expression and Refolding of Recombinant Bone Morphogenetic Protein-2.
Bone morphogenetic proteins belong to transforming growth factor [beta] superfamily which include TGF [beta], Activin, Nodals, Inhibins and Growth Differentiation Factors (GDFs) family. The members of TGF [beta] super-family have a vital role in embryonic development (1) and sending messages through smad signaling pathway (2). Over 20 BPM members have been identified to date (3) , among them BMP-2, BMP-3, BMP-4 and BMP-7 have been studied more than any others. BMP-2 is a cysteine rich protein that plays an important role in many stages of chondrocytes differentiation and maturation rather than osteogenesis in vivo. The mature BMP-2 is a disulfide -connected homo-dimer, composed of 114 amino acids derived from the C-terminal sequence of a 396 amino acid precursor polypeptide. The intra and inter chain disulfide bonds are essential for active structure formation and ligand binding to cell surface receptors.
Cysteine rich heterologous protein production in prokaryotic systems leads to inclusion body formation and protein aggregation (4,5). Since they are enclosed in inclusion bodies, purification of aggregated proteins is rather a convenient process while their refolding is a laborious and time-consuming procedure.
TGF beta family proteins have been proposed to have multiple beta sheets and hydrophobic structures, as they can minimize water solubility and induce improper protein refolding patterns (6).
Protein refolding procedure generally begins with aggregated protein extraction anu dissolving in high concentration chaotropic agents such as urea and guanidine hydrochloride (GuHCl). Chaotropic interaction unbraids entanglement structure of proteins and dissolves aggregated proteins in water. Afterwards, urea or GuHCl is replaced with additives or surfactants such as L-Arginine (7,8), L-proline (9), Glycerol (10) or detergents such as CHAPS (11), in order to prevent precipitation in the next stage of protein refolding process.
Generally, protein refolding method is an experimental technique -typically with less than 50% efficiency-and is highly dependent on protein type, refolding buffer compounds and additives.
One of the first and comprehensive studies on BMP-2 refolding was done by Vallejo (12). He showed that the refolding yield is particularly sensitive to protein concentration, temperature, pH, and the presence of aggregation inhibitors. However, the overall refolding yield obtained by him was 38% by optimizing the conditions for all parameters.
Refolded BMP-2 protein had the ability to induce osteogenesis in vivo when Sharapova et al applied it in a model of ectopic osteogenesis (13). They expressed and purified BMP-2 from Escherichia coli (E. coli) BL21 (DE3) inclusion body and refolded it using a buffer lacking a proper redox conditions. Although in previous reports the effects of pH (14) have been studied well enough to evaluate the refolding efficiency and biological activity of BMP-2, the influence of kind and quantity of different oxidoreductase agents on refolding efficiency has not been well established yet.
In this study, different oxidoreductase system effects on protein homodimeric formation procedure were compared and a simple method for protein dimer purification was established in addition to evaluation of the effects of changes in refolding process on protein activity.
Materials and Methods
Gene synthesis and cloning
Protein coding sequence of 114 N -terminal amino acid chain for bone morphogenetic protein2 (UniProt-KB-P12643) was retrieved from genbank |NM_ 001200.2| and optimized for expression in Origami 2(DE3) pLys strain of E. coli (Novagen). Putting BamHI and HindIII restriction sites at amino and car-boxyl ends, the construct was synthesized (GENEray
Biotechnology) and subcloned in pET28a (Novagen Inc., Madison, Wis). The recombinant plasmid was transformed to competent cells and colony PCR and construct digestion were employed for cloning validation.
Protein expression and extraction
For recombinant BMP-2 expression, the transform-ants were grown in LB culture media containing 15 [micro]g/ml kanamycin until [OD.sub.600]=l followed by induction with 0.2 mM IPTG for 6 hr at both 25 and 37[degrees]C. The harvested cells were lysed by cell lytic buffer (20 mM PBS, 500 mM NaCl, 1 mM EDTA, 100 [micro]/ml Lyso-zyme, Benzonase 80 u/ml, 0.1% Triton XI00) and centrifuged at 14000 g for 30 min. The supernatant contained total soluble proteins which were applied to a nickel-charged affinity resin column (Ni-NTA Agarose, Qiagen 30210) and his-tag affinity was purified with imidazole buffers (300 mM NaCl, 50 mM phosphate buffer pH=8.0 and 50 to 300 mM imidazole) for his-tag affinity purification. The remaining pellet containing inclusion bodies was resuspended in wash buffer (20 mM PBS, 1 mM EDTA, 2% Triton X100) and centrifuged at 26000 g fori5 min and then solubilized in inclusion body dissolving buffer (6M GuHcl, 0.1 M Tris Hcl pH=8.5, 1 mM EDTA, 50 mM DTT) and incubated for 2 hr at room temperature. The protein solution was then centrifuged at 14000 g for 15 min and DTT was removed by dialysis against 5 M GuHCl, 0.1 M Tris Hcl, pH=3.5 overnight. Finally, a Bradford assay was run for protein content estimation.
Protein refolding and purification
BMP-2 refolding was carried out by dilution of protein in refolding buffer (100 mM Tris/HCl pH=8.3, 5 mM EDTA, 250 mM NaCl, 0.5 M L-arginine) to decrease protein concentration and prevent aggregation. Two oxidoreductase systems (reduced glutathione/oxidized glutathione and Cysteine/Cystine) and different refolding methods were used to analyze disulfide bond formation as well as protein dimerization (Table 1). BMP-2 refolding was started by gradual addition of denatured protein to pre-cooled refolding buffer until the concentration fell below 0.2 mg/ml while stirring at 4 [degrees]C for 24 hr. The protein concentration increased to 1 mg/ml by cross flow filtration (Amicon ultra centrifugal filter) and redox system components were removed by dialysis against urea 6 M, 0.1 M Tris/HCl and 5 mm EDTA, pH=6. Dimeric protein was eluted by heparin column (Heparin sepharose [TM] 6 Fast Flow, GEHealth-care, 17-0998-01) at 0.3 and 0.7 MNaCl and purified protein was dialyzed against 20 mM ammonium acetate buffer, pH=4.8 and lyophilized.
SDS-PAGE and western blotting
Recombinant BMP-2 expression and refolding pattern were analyzed by non-reducing 12% SDS-PAGE. Separated proteins were electrophoretically transferred to nitrocellulose membranes by semi-dry blotting using a Dunn carbonate transfer buffer (10 mM [NaCHO.sub.3], 3 mM [Na2CO.sub.3], 20% methanol). The membranes were blocked for 2 hr using western blocker solution (Sigma, W0138) and incubated overnight at 4 [degrees]C, with anti-Histag (1:30000, Penta-His Antibody mouse monoclonal Qiagene, 1008288) as a primary antibody. The blots were washed three times with washing buffer (PBS-Tween-20, 0.05%) and incubated with the perox-idase-conjugated secondary rabbit anti mouse antibody (sigma A9044) for one hour at room temperature. The blots were visualized using ECL detection reagents (Sigma, CPS-1-120) and the films were scanned with a densitometer (GS-800, Bio-Rad).
Biological activity test of recombinant BMP-2
Biological activity of BMP-2 was measured by evaluation of its ability to increase the alkaline phosphatase activity (ALK) of a chondrogenic mouse embryonic carcinoma cell line, ATDC-5 (15). The ATDC5 cell line was purchased from the RIKEN Cell Bank (RCB-0565) and a positive control was purchased from R&D company (cat no: 355-BM). ALK activity of BMP-2 induced cell line was tested using Alkaline Phosphatase Yellow Liquid Substrate System for ELISA, containing p-nitrophenyl phosphate (pNPP) (Sigma P7998).
ATDC-5 cells were cultured in Dulbecco's modified eagle's medium DMEM-F12 (Invitrogen, 105 21331-020) supplemented with 5% Fetal Bovine Serum (FBS; Gibco Inc. Canada) and 50 mg/ml Non-Essential Amino Acid (NEAA) (Gibco Inc. Canada) without any antibiotic.
A Serum Free Medium (SFM) was prepared for assay with RPMI 1640 (Gibco Lot no: 1668798) as a basal medium supplemented with NAEE and 0.1% bovine serum albumin.
Assay for alkaline phosphatase activity
Briefly, SFM contained serial dilutions of recombinant BMP2 and commercial R&D BMP2 (0-500 ng/ml) was provided in a 96 well flat-bottom plate and ATDC-5 cells were plated and incubated for 5 days at 37[degrees]C in a humidified, 5% [CO.sub.2] atmosphere. After 5 days of culturing, cells were washed with PBS and enzyme activity was assayed by pNPP -a substrate in alkaline phosphatase assay buffer- and then plate was incubated at 37[degrees]C for 20 min. Next, the absorbance was measured at 405 run with microplate reader.
Analysis of cloning process
Synthetic coding sequence of BMP-2 which was restriction enzyme digested of pGH plasmid was sub-cloned into pET28 plasmid. After transformation of competent cells with recombinant plasmid, several colonies were selected on antibiotic plate for further analyses. Colony PCR using T7 primers (Figure 1) as well as restriction enzyme digestion of recombinant plasmid (Figure 2) amplified and released expected product sizes.
Identification of recombinant BMP-2 protein
SDS-PAGE banding pattern analysis of proteins extracted from 37[degrees]C cultured E. coli showed that the recombinant BMP-2 was exclusively expressed as an insoluble fraction and accumulated in cytoplasm as inclusion bodies. Inclusion body extracted proteins exhibited a sharp band between 17 to 20 kDa, corresponding to monomeric chain of BMP-2 (Figure 3). Similar result was also obtained following protein expression at 25 [degrees]C (data not shown).
Recombinant BMP-2 refolding results were assessed via non-reducing SDS-PAGE (Figure 3). Protein dimer formation in the refolding process accounts for approximately 40-50% at best.
Western blot analysis (Figure 4) using anti-HisTag which strongly reacted with N-terminal histidine tag of recombinant BMP-2 protein, confirmed that migrated bands between 17 to 20 kDa and near 25 kDa are related to the monomeric and dimeric forms of the protein, respectively.
Evaluation of recombinant protein refolding process
In order to analyze the efficiency of disulfide bond formation in BMP-2 protein, two oxidoreductase systems in refolding buffer were used for refolding process (Table 1). Figure 5 illustrates electrophoretic mobility pattern of heparin affinity purified BMP-2 which was refolded by different oxidoreductase systems. A ratio of 10/1 of reduced/oxidized components was used for method one refolding process of the recombinant protein (Table 1).
The electrophoretic mobility of recombinant BMP-2 which was refolded by method two protocol (Table 1) is represented in figure 4. In this method, the unfolded protein was diluted and incubated up to 48 hr in refolding buffer containing 0.1/0.1 mM GSFI/GSSG that catalyzes intra chain disulfide bond formation. Next, the solution was combined and incubated with equal volume/concentration of 5 mM/0.5 mM pretreated GSH/GSSG (product of method one) for two hours and then dialyzed. Figure 3 depicts electrophoretic pattern of refolded dimeric BMP-2 compared with that of monomeric fraction which are both eluted by 0.3 and 0.7 M NaCl, respectively.
Analysis of protein purification methods
Refolded BMP-2 was purified using two methods, histidine tag affinity purification and heparin affinity chromatography. His-tag affinity purification included two essential elements.
First, N-terminal histidine tag of recombinant protein was provided by expression vector and expressed as a fusion protein with BMP-2. Second, there was nickel-charged affinity resin column for protein purification.
Different concentrations of imidazole were used in elution buffer for affinity purification of BMP-2. However, no significant differences were observed in mon-omer/dimer separation (data not shown). Heparin affinity purification of refolded protein is presented in figure 3. Protein purification using elution buffers containing 0.3 and 0.7 M NaCl showed the best results in monomer/dimer separation.
Biological activity of recombinant BMP-2
The biological activity assay indicated that the refolded recombinant BMP-2 increased the ALK activity of ATDC-5 cell line as much as that of commercially available eukaryotic protein (Figure 6). Increasing the concentration of refolded BMP-2 applied onto ATDC-5 cell line resulted in induction of ALK activity in a dose- dependent manner. This is a practical assay for measurement of BMP-2 activity that can be performed with high-accuracy.
Bacterial expression of BMP-2 resulted in production of inclusion body and therefore, protein aggregation in cytoplasm. The aggregated protein can be solu-bilized and extracted from inclusion body under high concentration of urea and GuHCl. Native structure of protein can be restored by decreasing urea/GuHCl concentrations and replacing them with compounds which prevent protein aggregation and promote proper folding. In the next step, these compounds should be removed gradually and protein is solubilized in appropriate buffers, capable of maintaining its active structure. Cysteine-rich proteins require a proper oxidoreductase system for disulfide bond formation or rearrangement of incorrectly formed bonds.
In this study, synthetic coding sequence of BMP-2 protein was restriction digested and subcloned in pET28a plasmid and finally transformed in Origami[TM] strain of E. coll Verification of the insert and its orientation was approved by colony PCR amplification and restriction digestion analysis.
SDS-PAGE analysis of recombinant BMP-2 expression confirmed a high level of protein, aggregated as inclusion bodies and entirely not present in soluble fraction, in spite of decreasing IPTG induction temperature below 25 [degrees]C. In order to restore native structure and function of GuHCl solubilized BMP-2, two different protein renaturation experiments were run. GSH/GSSG and Cysteine/Cyctine oxidoreductase systems as well as two different protocols were employed for BMP-2 refolding process. There was no significant difference between two oxidoreductase systems in terms of dimeric structure improvement of BMP-2. On the other hand, increasing the concentration of either oxidoreductase components resulted in dimeric structure enhancement. However, the multimeric structure of BMP-2, which is the result of protein misfolding, simultaneously increases with rising in oxidoreductase components' concentration (Figure 5).
These misfolded multimeric structures have been reported in similar studies (13,16). It was concluded that there was a positive relationship between interchain disulfide bond formation and increase in concentration of oxidoreductase systems' components. However, no considerable biological activity of refolded protein was observed following the increase in oxidoreductase system concentration (data not shown).
In an attempt to decrease multimeric structure and at the same time increase purified dimeric protein as well as biological activity, a different refolding procedure was designed in addition to heparin affinity purification. First, the unfolded BMP-2 was diluted gradually in protein refolding buffer containing 0.1 mM /0.1 mM of GSH/GSSG for up to 48 hr and then dialyzed. Second, the dialyzed protein was pooled with an equal volume of BMP-2 pretreated with 5 mM 10.5 mM of GSH/GSSG and incubated for two hours. Our hypothesis was that the refolding of BMP-2 under this mild condition (0.1 mM /0.1 mM GSH/GSSG) results in correct formation of intrachain disulfide bonds and therefore monomeric renaturation. Pooling with 0.5 mM 15 mM of GSH/GSSG pretreated BMP-2-which is oxidized rather than being in reduced state- resulted in improvement of protein dimerization and thus activity. Finally, the monomeric and misfolded multimeric structures of BMP-2 were successfully eluted with high purity using a heparin affinity purification column (Figure 3).
In view of well-established methods available for protein refolding, our study presented a reproducible, practical and cost-effective method for BMP-2 growth factor production in E. coli bacterial system which is comparable with eukaryotic systems in terms of biological activity and stability.
The authors would like to thank Dr Mohammad-reza Gharaati for his kindly technical advisement. This study was supported by grants from Semnan University of Medical Sciences and Royan Institute.
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Davood Nasrabadi (1,2,3), Siamab Rezaeiani (4), Ali Sayadmanesh (4), Mohamadreza Baghaban Eslaminejad (2*), and Aliakbar Shabani (1*)
(1.) Department of Medical Biotechnology, Semnan University of Medical Sciences, Semnan, Iran
(2.) Department of Stem Cell and Developmental Biology, Cell Science Research Center, Roy an Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
(3.) Student Research Committee, Semnan University of Medical Sciences, Semnan, Iran
(4.) Department of Molecular Systems Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
(*) Corresponding authors: Aliakbar Shabani, Ph.D., Department of Medical Biotechnology, Semnan University of Medical Sciences, Semnan, Iran
Eslaminejad, Ph.D., Department of Stem Cell and Developmental
Biology, Cell Science Research
Center, Royan Institute for Stem
Cell Biology and Technology,
ACECR, Tehran, Iran
Tel: +98 23 33654187,
Fax: +98 21 22409314
Received: 8 May 2017
Accepted: 10 Jul 2017
Table 1. Protein refolding method Method one Method two 1, Dilution in refolding buffer containing 0.1 /0.1 mM reduced/ oxidized Dilution in refolding buffer containing oxidoreductase system/incubation for oxidoreductase system, incubation up to 48 hr 48 hr 2. Combining and incubating with 5 wM/0.5 mMGSH/GSSG-pretreated BMP- 2 for two hours and dialysis Oxidoreductase lined system: Oxidoreductase used system: 1. GSH/GSSG or 2. Cystein/Cystine 1. GSH/GSSG and 2. GSH/GSSG A: 2 mM/0.2 mM C: 2 mM/0.2 mM 0.1 mM/0.1 mM and 0.5 mM 15 mM B: 5 m.M/0.5 mM D: 5 mM/0.5 mM
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|Title Annotation:||Original Article|
|Author:||Nasrabadi, Davood; Rezaeiani, Siamab; Sayadmanesh, Ali; Eslaminejad, Mohamadreza Baghaban; Shabani,|
|Publication:||Avicenna Journal of Medical Biotechnology (AJMB)|
|Date:||Oct 1, 2018|
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