- Open Access
Expression and cytosolic assembly of the S-layer fusion protein mSbsC-EGFP in eukaryotic cells
© Blecha et al; licensee BioMed Central Ltd. 2005
- Received: 16 August 2005
- Accepted: 04 October 2005
- Published: 04 October 2005
Native as well as recombinant bacterial cell surface layer (S-layer) protein of Geobacillus (G.) stearothermophilus ATCC 12980 assembles to supramolecular structures with an oblique symmetry. Upon expression in E. coli, S-layer self assembly products are formed in the cytosol. We tested the expression and assembly of a fusion protein, consisting of the mature part (aa 31–1099) of the S-layer protein and EGFP (enhanced green fluorescent protein), in eukaryotic host cells, the yeast Saccharomyces cerevisiae and human HeLa cells.
Upon expression in E. coli the recombinant mSbsC-EGFP fusion protein was recovered from the insoluble fraction. After denaturation by Guanidine (Gua)-HCl treatment and subsequent dialysis the fusion protein assembled in solution and yielded green fluorescent cylindric structures with regular symmetry comparable to that of the authentic SbsC. For expression in the eukaryotic host Saccharomyces (S.) cerevisiae mSbsC-EGFP was cloned in a multi-copy expression vector bearing the strong constitutive GPD 1 (glyceraldehyde-3-phosophate-dehydrogenase) promoter. The respective yeast transfomants were only slightly impaired in growth and exhibited a needle-like green fluorescent pattern. Transmission electron microscopy (TEM) studies revealed the presence of closely packed cylindrical structures in the cytosol with regular symmetry comparable to those obtained after in vitro recrystallization. Similar structures are observed in HeLa cells expressing mSbsC-EGFP from the Cytomegalovirus (CMV IE) promoter.
The mSbsC-EGFP fusion protein is stably expressed both in the yeast, Saccharomyces cerevisiae, and in HeLa cells. Recombinant mSbsC-EGFP combines properties of both fusion partners: it assembles both in vitro and in vivo to cylindrical structures that show an intensive green fluorescence. Fusion of proteins to S-layer proteins may be a useful tool for high level expression in yeast and HeLa cells of otherwise instable proteins in their native conformation. In addition the self assembly properties of the fusion proteins allow their simple purification. Moreover the binding properties of the S-layer part can be used to immobilize the fusion proteins to various surfaces. Arrays of highly ordered and densely structured proteins either immobilized on surfaces or within living cells may be advantageous over the respective soluble variants with respect to stability and their potential interference with cellular metabolism.
- HeLa Cell
- Enhanced Green Fluorescent Protein
- Assembly Product
- Frame Fusion
Bacterial cell surface layers (S-layer) as the outermost cell envelope components are a common feature of many bacteria and archaea species (for review see [1, 2]). With few exceptions S-layers consist of a single species of subunits that occasionally is posttranslationally modified by phosphorylation , or glycosylation [4, 5]. S-layer monomers assemble to two-dimensional highly porous arrays with either oblique, square or hexagonal symmetry. The interactions between the S-layer subunits as well as between the S-layer and the supporting envelope can be disrupted in a reversible manner by cation substitution or high concentrations of chaotropic agents . Upon removal of the denaturing agent the isolated S-layer subunits assemble in vitro into regular arrays exhibiting structural features of the authentic cell surface layer. Contrary to the situation in vivo, the in vitro self-assembly process of S-layer proteins in solution can also result in double layer sheets or in tube-like structures .
S-layers have been recognized as important structures for biotechnological applications . However, large-scale preparation of S-layers from the authentic organisms is sometimes limited. For example, some bacterial strains have been reported to loose their ability to produce S-layers under laboratory conditions . Due to alterations in the cultivation conditions expression of truncated forms of the S-layer protein may result in the loss of S-layer sheets . To circumvent such difficulties recombinant S-layer proteins have been heterologously produced in prokaryotic systems, like E. coli, Bacillus subtilis, Lactobacillus casei , or Lactococcus lactis . For example, high level expression of the S-layer protein SbsC from Geobacillus stearothermophilus ATCC 12980 has been reported in E. coli . SbsC possesses an N-terminal secretion signal of 30 amino acids (aa) that is cleaved off during secretion, a secondary cell wall polymer (SCWP)-binding domain (aa 31–258), and a central portion responsible for formation of lattice symmetry and self-assembly . Upon expression in E. coli, the mature S-layer protein mSbsC(31–1099) with an apparent molecular mass of 112 kDa forms monolayer cylinders and spirally wound sheets-like structures in the cytosol that can be recovered from the insoluble fraction upon cell lysis. Neither deletion of the C-terminal 179 aa (rSbsC(31–920))  nor fusion of this truncated form with major birch pollen antigen Bet v1 (rSbsC(31–920)-Betv1) interferes with the assembly process and the oblique lattice symmetry. Interestingly, the Bet v1 epitope was accessible to antibodies demonstrating that the fused portion is protruding from the respective assembly structure . Contrary to the situation of SbsC, recombinant S-layer protein SbpA from B. sphaericus CCM 2177 and its derivatives fail to assemble in the E. coli cytosol, but form insoluble inclusion bodies .
In the present study we addressed the question whether the cytosol of eukaryotic host cells can provide a suitable environment for the formation of S-layer self assembly products, despite the presence of numerous chaperons and proteases. Assembly of S-layer fusion proteins could provide a simple purification scheme for soluble proteins, especially if the formation of their native structures depends on the conditions of the eukaryotic cytosol. In addition, such fusion proteins could stabilize proteolytically sensitive proteins and thus increase their yield.
We used the yeast Saccharomyces cerevisiae and the HeLa cells as eukaryotic model organisms for expression of a bifunctional S-layer fusion protein, consisting of mature SbsC (aa 31–1099) and the enhanced green fluorescent protein (EGFP).
Expression of mSbsC-EGFP in E. coli
When recrystallization was performed in the presence of G. stearothermophilus wild type strain ATCC 12980 devoid of its native S-layer due to Gua-HCl treatment, cells were covered with a green fluorescent layer indicating binding to the SCWP (data not shown). The same result was obtained with other G. stearothermophilus strains (DSM 297, DSM 13240 and DSM 1550), but not with the Gua-HCl treated yeast strain BY4741.
Expression of mSbsC-EGFP in S. cerevisiae
TEM analysis of recombinant mSbsC-EGFP structures in yeast
Expression of mSbsC-EGFP in HeLa-cells
The ORFs of mSbsC and EGFP were fused in-frame within the vector pEGFP-N1. HeLa cells were liposome-transfected with the resulting plasmid pmSbsC-EGFP-N1. 16 h after transfection adherent HeLa cells exhibit green fluorescent filamentous structures. The fluorescence was exclusively restricted to these structures, other intracellular areas were competely devoid of green fluorescence. Obviously the fluorescent structures result from self assembly of mSbsC-EGFP within the cytosol. The morphology of these structures is very similar to that of the assembly products formed in mSbsC-EGFP producing yeast cells.
Despite of their potential for biotechnological application only few S-layers genes have been identified and were used for genetic modification and recombinant production. Usually prokaryotic systems like Lactobacillus casei, B. subtilis, E. coli (for review see: ) and Lactococcus lactis  were used for heterologous expression.
Our report describes for the first time the expression of a S-layer fusion protein in eukaryotic host cells. Because of the ability of mSbsC to form sheet-like and cylindrical structures in the cytosol of E. coli , we decided to use this S-layer protein for fusion with EGFP. Expression was first investigated in the yeast S. cerevisiae, one of the best-studied eukaryotic organism. We observed no alterations of the cell shape and only a slightly reduced vegetative growth, possibly reflecting the high energy demand due to the constitutive high level synthesis of 139 kDa mSbsC-EGFP. Western blot analysis of insoluble material with anti-GFP antibody gave no indication for N-terminal proteolytic degradation of the recombinant protein as observed in E. coli. Possibly the organization of mSbsC-EGFP in assembled structures confers protection from ubiquitin-mediated degradation in yeast. In respect to protein stability S. cerevisiae seems to be a superior expression system. Fluorescence microscopy revealed that yeast transformants exhibited an intense green fluorescence indicating proper folding of the EGFP part within mSbsC-EGFP. In line with the formation of self-assembly structures in the cytosol, the fluorescence pattern differs significantly from that of EGFP-expressing yeast cells. TEM studies revealed the presence of closely packed cylindrical structures with regular symmetry comparable with those obtained after in vitro recrystallization. Our study demonstrates that the assembly process of SbsC-EGFP is not affected by the presence of eukaryote-specific cytosolic chaperons, like members of the CCT family .
Recently it was reported that some S-layer monomers assemble on hydrophobic surfaces. S-layer proteins of the strains G. stearothermophilus PV72/p2 and NRS 2004/3a form protein monolayers on substrates like silicon wafers with a native oxide layer . The self-assembly structures of SbsC-fusion proteins in yeast are not associated with the inner surface of the plasma membrane or cellular organelles despite their hydrophobic membranes. Obviously the hydrophobic membrane patches do not act in anchoring assembled S-layer structures.
As in yeast cells, mSbsC-EGFP monomers self assemble into filamentous structures within the cytosol of HeLa cells that are neither associated with subcellular structures nor affect the cell shape. We did not observe necrotic or apoptotic events in the transfected cells that expressed mSbsC-EGFP (data not shown). The detection of a single band of the expected molecular weight in Western blot analysis with anti-GFP antibodies indicates that the recombinant protein is stable and not subjected to N-terminal degradation.
A positively charged N-terminal domain of S-layer proteins directly interacts via electrostatic forces with the negatively charged SCWP whose chemical composition is identical in G. stearothermophilus wild-type strains . In our study we show that fusion of EGFP to the mSbsC, resulting in an extension of the S-layer protein by ~240 aa, does not interfere with the binding.
Our results show that the mSbsC-EGFP fusion protein is efficiently synthesized, and self-assembles under the physiological conditions of the cytosol of eukaryotic cells. Both in yeast and human cells cytosolic accumulation of S-layer self assembly products is not accompanied by proteolytic degradation. The green fluorescence of mSbsC-EGFP suggests that both in vitro and in vivo folding of both protein portions within the fusion protein is independent, and not affected by each other. This observation opens the possibility to fuse other proteins, e.g. enzymes, to the S-layer part in order to obtain functional fusion constructs in a densely packed and stable structure.
Fusion of otherwise instable proteins to S-layer proteins may be a useful tool for their high level expression in eukaryotic cells. The self assembly properties of the fusion proteins can be exploited to purify them by simple centrifugation steps from cell lysate. By engineering a suitable protease cleavage site between the S-layer and the fused protein part, incubation of the assembly products with the respective proteases could allow separation and subsequent purification of the protein of interest. Arrays of highly ordered and densely structured S-layer fusion proteins can efficiently be immobilized on a variety of surfaces, either directly or upon treating with SCWP.
Besides technical applications, an ordered aggregation of S-layer fusion proteins within living cells may offer novel strategies for cell manipulation. For example, if expression of proteins would interfere with cellular functions, e.g. as a result of intracellular transport, fusion to an S-layer protein permits their retention in the cytosol. "In vivo affinity chromatography" may be another potential field for applying S-layer fusion proteins. Enrichment of soluble biomolecules within living cells may be achieved by assembly structures consisting of fusion proteins between the respective receptor and a suitable S-layer protein.
Geobacillus (G.) stearothermophilus ATCC 12980
G. stearothermophilus DSM 1550 (German Collection of Microorganisms and Cell Cultures (DSMZ) GmbH, Braunschweig, Germany)
G. stearothermophilus DSM 13240 (DSMZ)
G. stearothermophilus DSM 297 (DSMZ)
Escherichia (E.) coli DH5á (BRL)
E. coli BL21(DE3) (Invitrogen)
Saccharomyces (S.) cerevisiae BY4741 (EUROSCARF)
HeLa cells (kind gift of Frank Pfennig, Institut für Zoologie, Technische Universität Dresden, Germany)
#1: 5' TATATATACATATGGCAACGGACGTGGCGACGGTC 3'
#2: 5' TATATATACTCGAGCGATGCTGATTTTGTACCAATTTG 3'
#3: 5' TATATATACTCGAGATGGTGAGCAAGGGCGAGGAG 3'
#4: 5' TATATATAGCTCAGCTTACTTGTACAGCTCGTCCATGC 3'
#5: 5' TATATATAGGATCCATGGCAACGGACGTGGCGACGGTC 3'
#6: 5' TATATATAGGTACCTCACTATTACTTGTACAGCTCGTCCATGC 3'
#7: 5' TATATATACTCGAGATGGCAACGGACGTGGCG 3'#8: 5' TATATATACCGCGGCGATGCTGATTTTGTACCAATTTG 3'
Cultivation of G. stearothermophilus strains, isolation and recrystallization of S-layer proteins
Batch cultures of the G. stearothermophilus strains were grown in tryptone-enriched LB-medium at 55°C (strain DSM 13240 at 65°C) to an OD600 of 0,6. Surface proteins attached to the cell wall layer via noncovalent forces were removed by Guanidine-HCl (Gua-HCl) treatment of cells from a 500 ml culture. Cells were washed 3 times in distilled water, suspended in 10 ml of 5 M Gua-HCl and incubated for 30 min on ice with occasional mixing. Cells devoid of their S-layers were recovered by centrifugation at 8,000 × g and washed twice with 5 M Gua-HCl. For preparation of S-layer proteins the supernatant obtained after centrifugation at 40,000 × g was dialyzed against distilled water for 18 h.
Preparation of genomic DNA and DNA-cloning
Genomic DNA was isolated with the QIAGEN Genomic-tip 100 kit according to the manufacturer's instruction. Plasmid DNA was prepared with the "Wizard® SV Gel and PCR Claen-up system kit" (Promega).
Cloning in pET17b
DNA encoding mSbsC(31–1099) was PCR-amplified with primers #1 and #2, using total DNA of G. stearothermophilus ATCC 12980 as a template. An ATG initiation codon was introduced 5'to the open reading frame by primer #1. The PCR-product was cut with Nde I and Xho I and ligated with plasmid pET17b (Novagen) to yield plasmid pET17b-mSbsC_oT.
The Xho I and Bpu 1102I sites of pET17b-mSbsC_oT were used to insert the EGFP reading frame, which was PCR-amplified from vector EGFP-N1 (Clontech) with primers #3 and #4. Primer #3 introduced a 5'-flanking Xho I-site in the PCR product, while primer #4 generated a 3'-flanking Bpu 1102I-site and introduced a TAA termination codon. The PCR-product was cut with Xho I and Bpu 1102I and ligated with pET17b-mSbsC_oT to yield plasmid pET17b-mSbsC_oT-EGFP.
Cloning in p426-GPD
A DNA fragment encoding mSbsC was PCR-amplified as described above with primers #5 and #2, cut with Bam HI and Xho I, and ligated with the S. cerevisiae expression vector p426-GPD, which bears the strong GPD promoter . The resulting plasmid p426-GPD-mSbsC_oT was used for in frame fusion the EGFP orf, which was amplified with primers #3 and #6. The respective PCR product harbours a 5' Xho I site and at the 3'-end three consecutive termination codons followed by a Kpn I restriction site. Thereby plasmid p426-GPD-mSbsC_oT-EGFP was created.
Plasmid p426-GPD-EGFP for expression of EGFP in yeast was created by ligation of the PCR-fragment encoding the EGFP orf into p426-GPD via the flanking Xho I and Kpn I sites. Plasmids p426-GPD-mSbsC_oT-EGFP and p426-GPD-EGFP were propagated in E. coli DH5α and transformed into the S. cerevisiae wild type strain BY4741.
Cloning in pEGFP-N1
The reading frame coding for mSbsC was amplified with primers #7 and #8 and subsequently integrated within the Xho I and Sac II restriction sites in the vector pEGFP-N1 (Clontech) as an in frame fusion with the EGFP-ORF.
The resulting plasmid pmSbsC-EGFP-N1 was propagated in E. coli DH5α and transfected into HeLa cells.
Transfection of HeLa cells
For transient transfection with plasmid pmSbsC-EGFP-N1, 2,5 × 105 cells were plated on chamber slides (Nunc) and incubated after one day with TFX™-20 liposome reagent (Promega) and 3 μg DNA for 1 h. Subsequently DMEM with high glucose and 10 % (v/v) fetal calf serum (PAA laboratories) was supplemented. After over night cultivation transfected cells were analysed by Western blot and fluorescence microscopy.
Isolation and purification of recombinant S-layer proteins from E. coli
E. coli BL21(DE3) was used as a prokaryotic host for the expression of mSbsC-EGFP. E. coli transformants bearing pET17b-mSbsC-EGFP were cultivated in LB medium containing 100 mg/l ampicillin at 30°C to an OD600 of 0,4. S-layer synthesis was initiated by adding IPTG to a final concentration of 0,5 mM.
8–16 h after induction cells obtained from a 500 ml culture were harvested by centrifugation at 10,000 × g for 10 min; 4°C. The cell pellet was washed 3 times with ice-cold distilled water and resuspended in 10 ml Tris-buffer (10 mM Tris, pH 7,5; 1 mM AEBSF hydrochloride (AppliChem)) containing 1% (v/v) Triton X-100. After disruption of cells by French press (25,000 PSI pressure, at 4°C), soluble and insoluble fractions were separated by centrifugation at 20,000 × g for 30 min at 4°C. Nucleic acids were removed from the pellet fraction by treatment with DNase I (1 mg/ml) and RNase A (1 mg/ml) in Tris-buffer. After three washing steps with Tris-buffer the insoluble material was denatured in 5 ml 5 M Gua-HCl (in 10 mM Tris pH 7,5). The suspension was stirred at room temperature (RT) for 30 min and centrifuged for 30 min at 40,000 × g (10°C). Renatured S-layer proteins were obtained by dialyzing the supernatant twice against 5 l of distilled water or Tris-buffer over night at 4–8°C using dialysis tubes with an exclusion size of 14 kDa.
For further purification the suspension containing renatured S-layer proteins was centrifuged at 12,000 × g for 30 min, the pellet washed 3 times with distilled water or Tris-buffer and dissolved in 3 M Gua-HCl in Tris-buffer. After a final centrifugation step (40,000 × g; 30 min) the clear supernatant was subjected to FPLC using a Sephacryl™ S-300 column (Pharmacia Biotech). Size exclusion chromatography was performed under denaturing conditions (3 M Gua-HCl in Tris-buffer) at RT with a flow rate of 0,5 ml/min. Fractions containing mSbsC-EGFP were dialyzed against dH2O over night and used for further analysis.
Isolation and purification of recombinant S-layer proteins from S. cerevisiae
Constitutive expression of S-layer protein coding genes was obtained by growing transformants of S. cerevisiae strain BY4741 bearing plasmid p426-GPD-mSbsC-EGFP in YNB medium (Invitrogen) supplemented with Leu, His, Met and glucose as carbon source. 500 ml of an exponential culture (OD600 = 1) were centrifuged at 5,000 × g for 3 min and 20°C. Cells were washed 3 times with Tris-buffer and subsequently lysed by osmotic swelling of protoplasts obtained by treatment with zymolyase-20T (ICN) as described . S-layer self assembly products were pelleted from the suspension by centrifugation at 20,000 × g.
Isolation and purification of recombinant S-layer proteins from HeLa cells
4 × 106 HeLa cells were transiently transfected with pmSbsC-EGFP-N1. After cultivation for 16 h cells were harvested by trypsin treatment followed by three washing steps with 1 × PBS w/o Ca2+, Mg2+ (PAA-Laboratories). Cell lysis was performed by 30 strokes in a dounce homogenizer in the presence of 0,1 % (v/v) Triton X-100, 1 mM AEBSF and Pi-cocktail (protease inhibitor mix; Roche). The cell lysate was centrifuged at 20,000 × g, and the resulting supernatant and pellet fractions were analysed in a Western blot.
Sample preparation and SDS-polyacrylamide gelelectrophoresis were carried out as described by Laemmli . Unless otherwise indicated 10 μg of protein were separated on 7,5% (w/v) acrylamide gels. For Westernblot analysis proteins were transferred onto a PVDF membrane (Millipore) and probed with monoclonal mouse antibody directed against the GFP epitope (Boehringer Mannheim). Detection of bound antibodies was performed with horseradish peroxidase (HRP)-conjugated secondary antibodies and the ECL-Plus Kit (Amersham Pharmacia Biotech). As positive control for immunreactivity of anti-GFP antibodies whole cell extract of EGFP expressing S. cerevisiae transformants was used (Fig. 4B).
Whole yeast cells and spheroplasts were fixed and prepared for electron microscopy as described by Waterham et al. . Immunolabeling was performed on ultrathin sections of Unicryl-embedded cells using polyclonal rabbit anti-GFP antibodies and 15 nm colloidal gold-conjugated goat anti-rabbit secondary antibodies (Amersham). Negative staining of osmotically swollen protoplasts and FPLC-purified recrystallized mSbsC-EGFP was done with 3% (w/v) ammonium-molybdate, pH 7,2 and examined in a Philips CM10 Transmission Electron Microscope.
Standard DNA techniques were as described . Yeast cells were transformed by the lithium acetate method . GENOMED™ columns were used for isolation of DNA fragments from agarose gels. The correct sequence of all constructs was confirmed by DNA sequencing with the dideoxy-chain termination method  using 5'-IRD800 labelled primers (MWG-BIOTECH). A Thermo Sequenase fluorescent labelled primer cycle sequencing kit with 7-deaza-dGTP (Amersham) was employed for sequencing with the LI-COR DNA sequencer 4000 (MWG-BIOTECH). Protein concentrations were determined by the Lowry method (BioRad).
This work was supported by a grant of the Saxonian Ministry of Science and the Fine Arts. We thank S. Selenska-Pobell, FZ Rossendorf for providing strain ATCC 12980 and S. Tokalov, Institut für Zoologie, Technische Universität Dresden for laser scan microscopy.
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