Nowadays, biotechnological processes play a pivotal role in target protein production. In this context, Chinese Hamster Ovary (CHO) cells are one of the most prominent cell lines for the expression of recombinant proteins and revealed as a safe host for nearly 40 years. Nevertheless, the major bottleneck of common in vivo protein expression platforms becomes obvious when looking at the production of so called “difficult-to-express” proteins. This class of proteins comprises in particular several ion channels and multipass membrane proteins as well as cytotoxic proteins. To enhance the production of “difficult-to-express” proteins, alternative technologies were developed, mainly based on translationally active cell lysates. These so called “cell-free” protein synthesis systems enable an efficient production of different classes of proteins. Eukaryotic cell-free systems harboring endogenous microsomal structures for the synthesis of functional membrane proteins and posttranslationally modified proteins are of particular interest for future applications. Therefore, we present current developments in cell-free protein synthesis based on translationally active CHO cell extracts, underlining the high potential of this platform. We present novel results highlighting the optimization of protein yields, the synthesis of various “difficult-to-express” proteins and the cotranslational incorporation of non-standard amino acids, which was exemplarily demonstrated by residue specific labeling of the glycoprotein Erythropoietin and the multimeric membrane protein KCSA.
Citation: Thoring L, Wüstenhagen DA, Borowiak M, Stech M, Sonnabend A, Kubick S (2016) Cell-Free Systems Based on CHO Cell Lysates: Optimization Strategies, Synthesis of “Difficult-to-Express” Proteins and Future Perspectives. PLoS ONE 11(9): e0163670. https://doi.org/10.1371/journal.pone.0163670
Editor: Nediljko Budisa, Berlin Institute of Technology, GERMANY
Received: May 27, 2016; Accepted: September 11, 2016; Published: September 29, 2016
Copyright: © 2016 Thoring et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work is supported by the European Regional Development Fund (EFRE) and the German Ministry of Education and Research (BMBF, No. 0315942, 0312039 and KMUinnovativ: Biotechnologie - BioChance, No. 031A511) and the German Research Foundation (DFG Priority Programme 1623).
Competing interests: The authors have declared that no competing interests exist.
Nowadays, production of recombinant proteins plays a pivotal role in the pharmaceutical industry. In particular, genetically engineered mammalian cells have become the predominant system for the manufacturing of proteins for clinical applications . Human tissue plasminogen activator was one of the first therapeutic proteins, produced in mammalian cell culture by Genentech in 1986 [2,3]. Currently Chinese Hamster Ovary (CHO) cells are the most popular and standardized cell line for recombinant protein production [4,5]. Nearly 70% of all pharmaceuticals are produced in engineered CHO cells [6,7]. There are several reasons for the decision to use CHO cells as an industrial working horse. For large scale industrial production of recombinant drugs, fermentation processes are preferentially performed in suspension cultures. CHO cells can be easily adapted and grown in suspension cultures, while serum-free and chemically defined media can be applied, which is advantageous with regard to Batch-to-Batch reproducibility . Additonally, fermentation of CHO cells is cost-saving and favorable due to safety reasons . Moreover CHO cells are safety approved for nearly 30 years (FDA) and therefore suitable for industrial large scale production processes . CHO cells were chosen as a preferable system for protein production due to the fact that this expression platform enables a high similarity of biochemical properties compared to the origin of recombinant target proteins . Consistently, recombinant proteins, produced in CHO cells, often show correctly folded structures and appropriate posttranslational modifications, e.g. harboring human like glycosylations . These qualities emphasize the ability to generate functional, glycoprotein therapeutics [2,11].
The production of certain specific target proteins of eukaryotic origin often posed issues in in vivo expression platforms. These so called “difficult-to-express” proteins cover various types of membrane proteins, including ion channels, multi-pass membrane proteins and G protein coupled receptors, as well as proteins that exhibit cytotoxic effects on the host cell during overexpression. To circumvent the bottlenecks of in vivo protein production systems, tailor-made cell-free protein synthesis systems have been developed, based on different translationally active cell extracts of prokaryotic and eukaryotic origin [12–14]. The choice of the individual cell-free platform depends on the requirements necessary for the target protein and its subsequent application. In general, prokaryotic cell-free systems are mainly based on lysates generated from Escherichia coli (E.coli) [15–19]. These systems, suitable for the high yield production of proteins, are limited in the implementation of posttranslational modifications . Eukaryotic cell-free systems represent an alternative option for the production of difficult-to-express proteins. In general, these systems can be divided into two classes: Cell-free systems harboring endogenous microsomal structures and systems without any endogenous membrane compartments [21,22]. Prominent candidates of lysates without endogenous vesicles are rabbit reticulocyte lysates and wheat germ lysates [23–28].
Lysates, based on rabbit reticulocytes, are long standing and well-known cell-free systems [29,30] which were often used for fundamental research studies [31–33]. Nevertheless, rabbit reticulocyte lysate system exhibits many disadvantages including a laborious and cost intensive preparation strategy, low protein synthesis rates and the requirement to supplement exogenous vesicular structures, e.g. canine microsomes , in order to obtain functional posttranslationally modified proteins.
Wheat germ systems can be used for high yield production of proteins and automation technologies are available . The major bottleneck of the wheat germ system is the limitation in posttranslational modifications due to the absence of endogenous microsomal structures. Therefore, the generation of novel cell-free systems needs to combine the preparation of endogenous microsomes for the synthesis of posttranslationally modified proteins and the high-yield production of functional proteins. In this context, various studies revealed multiple systems originating from different eukaryotic sources, including insect cells [36–40], plant cells [41–44] and mammalian cells [45,46]. Recent studies performed by Broedel et. al. [47,48] showed initial results regarding the cell-free synthesis based on CHO cells. To close the gap between applied research and industrial protein production, this system has subsequently been further developed.
We describe the diversity of cell-free protein synthesis based on CHO cell lysate. Optimization and improvement of protein yields as well as the ability to produce different classes of “difficult-to-express” proteins is demonstrated. Subsequently the cotranslational incorporation of non-standard amino acids in CHO lysate systems was exemplified by the cell-free production of fluorescently labeled glycoproteins and membrane proteins.
Materials and Methods
Cell-free protein syntheses in CHO lysates were performed using either vector DNA or linear DNA templates generated by polymerase chain reaction (PCR). Different vector backbones harboring a firefly luciferase (Luc) gene and internal ribosomal entry sites were tested in cell-free systems. This study included the following plasmids: pIX3.0-CRPV(GCT)-Luc, pIX3.0-EMCV-Luc, pcDNA3.1-CRPV(GCT)-Luc and pT7CEF1-EMCV-Luc. If not stated differently all vector based DNA constructs are based on a common in vitro protein synthesis pIX3.0 vector backbone (Biotech Rabbit) containing regulatory sequences for transcription and translation. A T7 promotor and a T7 terminator constituted regulatory sequences for transcription. For translation initiation an internal ribosomal entry site (IRES) of cricket paralysis virus was included into the 5´UTR and the start codon triplet of the gene of interest was exchanged from ATG to GCT, as it was shown in previous studies (Broedel et. al. 2014). The following proteins were selected as model proteins for initial tests: Luciferase (Luc) (cytosolic protein, 60.6 kDa), enhanced yellow fluorescent protein eYFP (cytosolic protein, 26.9 kDa) and erythropoietin including melittin signal peptide (Mel-EPO) for efficient translocation of proteins into microsomal structures of the CHO lysates (glycosylated protein, 19.7 kDa) with two deleted N-glycosylation sites at asparagine 52 and glutamine 110. To evaluate the performance of the CHO lysate cell-free protein synthesis system, different classes of membrane proteins were synthesized covering ion channels, G protein coupled receptors as well as multi-pass transmembrane proteins. During initial experiments different vector backbones and IRES were evaluated regarding their performance in CHO lysate based cell-free systems.
Templates for analyzing the ability of the CHO based cell-free system to synthesize proteins from linear DNA constructs were amplified by PCR. PCR was performed by using Hot Star HiFidelity polymerase (Qiagen) and following the manufacturer´s protocol. For this purpose the plasmids pIX3.0-CRPV(GCT)-Luc and pIX3.0-CRPV(GCT)-EPO were used in the PCR as general DNA templates. Adapter primers N-0 (5´ATG ATA TCT CGA GCG GCC GCT AGC TAA TAC GAC TCA CTA TAG GGA GAC CAC AAC GGT TTC CCT CTA GAA ATA ATT TTG TTT AAC TTT AAG AAG GAG ATA AAC AAT G 3´) and C-0 (TAA TAA CTA ACT AAC CAA GAT CTG TAC CCC TTG GGG CCT CTA AAC GGG TCT TGA GGG GTT TTT TGG ATC CGA ATT CAC CGG TGA TAT CAT) were used to amplify linear DNA-templates. Each of the adapter primers has overlap sequences which fuse regulatory sequences necessary for translation and transcription to the gene of interest.
Cell-free protein synthesis
Cell-free synthesis reactions were performed using CHO cell derived translationally active lysates. Lysates were prepared from cultured, exponentially grown CHO cells as described in previous studies . The protein synthesis processes were conducted in coupled transcription/translation reactions in a final volume of 20 to 50 μl. The reactions were incubated in a thermomixer (Eppendorf) for 3 h at 30°C and 600 RPM. Protein synthesis reactions were composed of 40% (v/v) of translationally active lysate supplemented with HEPES-KOH (pH 7.5, f.c. 30 mM), sodium acetate (f.c. 100 mM), Mg(OAc)2 (f.c. 3.9 mM), KOAc (f.c. 150 mM), amino acids (100 μM), spermidin (f.c. 0.25 mM), DTT (2.5 mM) and energy generation components including creatine phosphokinase (f.c. 0.1 mg/ml), creatine phosphate (20 mM), ATP (1.75 mM) and GTP (0.3 mM). If not reported otherwise, 60 ng/μl of plasmid DNA was added to the translation reaction. To enable DNA transcription to mRNA during cell-free protein synthesis, 1 U/μl T7 RNA polymerase, 0.3 mM of UTP and CTP and 0.1 mM of the cap analogue m7G(ppp)G were added to the reaction. Cell-free protein synthesis reactions were supplemented with radioactive 14C leucine (f.c. 50 μM, specific radioactivity 66.67 dpm/pmol) for radiolabeling of produced proteins, in order to allow the further analysis of synthesized proteins by autoradiography and liquid scintillation counting.
Enrichment of membrane and secreted proteins into microsomal structures was investigated by repetitive translation cycles. After each translation step translation mixture was separated into microsomal fraction and supernatant by centrifugation (16000xg, 15 min, 4°C). A 5 μl aliquot of each fraction was taken for further analysis. Microsomal fraction was newly resuspended using freshly prepared translation mixture without vesicles to start a new translation cycle and thereby enabling multiple addressing of microsomes.
Luciferase assay and western blot
Functionality of cell-free synthesized firefly luciferase was analyzed using Luciferase Assay Reagent (LAR, Promega). 50 μl of LAR were added to 5 μl of translation mixture. Subsequently luciferase induces a light reaction by catabolizing LAR, which was detected by a luminometer (LB941, Berthold, Germany). The concentration of active protein was determined by using a calibration curve. Additionally, cell-free produced luciferase was monitored by western blot analysis according to the manufacturer´s instructions using an IBlot device (Lifetechnologies). For this purpose, a primary rabbit anti luciferase IgG monoclonal antibody (St. John´s Laboratory) was applied for analysis. Detection of luciferase protein band was accomplished by using a secondary anti rabbit IgG antibody coupled to horseradish peroxidase (HRP). The addition of ECL reagent (Promega) led to a light reaction that was detected by a Typhoon TRIO+ Imager system (GE Healthcare).
Analysis of radio labeled proteins
The yields of radiolabeled proteins were determined by hot TCA precipitation. Therefore 5 μl of translation mixtures were transferred to a glass tube, 3 ml of 10% TCA/ 2% casein hydrolysate solution were added and boiled for 15 min at 80°C followed by incubation in an ice bath for 30 min. Precipitated proteins were transferred to membrane filters (Macherey Nagel), using a vacuum filtration device (Hoefer). Dried filters were placed into scinitillation tubes and 3 ml of scintillation cocktail (Zinsser Analytik) was added to the tubes. Radioactivity of samples was analyzed using a LS6500 Multi-Purpose scintillation counter (Beckman Coulter). The molecular mass of radiolabeled, cell-free synthesized proteins was determined by SDS-PAGE followed by autoradiography. The first step of sample preparation included an acetone precipitation of synthesized proteins. Therefore 5 μl of translation mixture and 45 μl of Millipore water were supplemented with 150 μl ice cold acetone. Samples were chilled on ice for at least 15 min. Afterwards precipitated proteins were centrifuged at 16000xg and 4°C for 10 min. Acetone was removed from the samples and pellets were dried at 45°C for 1 h in a thermomixer. Dried protein pellets were resuspended in LDS sample buffer (NUPAGE LDS sample buffer supplemented with 50 mM DTT) and samples were separated on precast non-reducing NUPAGE SDS-PAGE gels for 35 min at 200 V. SDS-PAGE gels harboring the separated proteins were stained with Coomassie blue solution (SimplyBlue SafeStain, Life technologies). Subsequently, gels were dried on a Whatman paper for 60 min at 70°C (Unigeldryer 3545D, Uniequip). Dried gels, harboring radiolabeled proteins, were exposed to phosphor screens. Finally, radiolabeled proteins were visualized using a phosphor imager system (Typhoon TRIO+ Imager, GE Healthcare).
Fluorescence analysis of eYFP fusion proteins
Cell-free synthesized eYFP and eYFP fusion proteins were analyzed using a Typhoon TRIO + Imager system (Excitation 488 nm, emission filter 526 nm short-pass; GE Healthcare). 5 μl of translation mixture was diluted with 20 μl of PBS and transferred to a μ-Ibidi slide for further analysis (Ibidi GmbH, Munich, Germany). The quantification of fluorescence intensity was performed by using Image Quant TL software.
Residue specific labeling of proteins using BODIPY-TMR-Lysine
An alternative labeling of cell-free produced proteins was conducted by cotranslational incorporation of BODIPY-TMR-Lys. A final concentration of 2 μM BODIPY-TMR-Lys was supplemented to the cell-free synthesis reaction. BODIPY-TMR-Lys labeled proteins were separated on SDS-PAGE and analyzed by detecting in-gel fluorescence. SDS-PAGE was performed as described in part 2.4 followed by a 30 min incubation in a 50% methanol/water solution at room temperature. Fluorescence signals of labeled proteins were visualized using a Typhoon TRIO + imager (GE Healthcare).
Application of different plasmid types for cell-free protein synthesis in translationally active CHO cell lysates
Cell-free production of proteins generally requires a DNA template or RNA to start synthesis of the desired target protein. Nowadays, different types of plasmids are available that can be applied directly to cell-free systems of prokaryotic and eukaryotic origin. A few DNA structure characteristics need to be fulfilled to enable the synthesis of chosen proteins in cell-free systems based on extracts from CHO cells. These requirements can be divided into two parts, which cover DNA elements essential for transcription and translation. Our newly developed cell-free system based on CHO cell lysates requires a T7- promoter- and terminator sequence introduced upstream of the gene sequence to realize transcription of RNA conducted by T7 RNA polymerase. DNA templates for the translation reaction comprises a ribosomal binding site for initiation of the translational process. As described earlier, an insertion of the Internal Ribosomal Binding Sites (IRES) for cap independent initiation of the translation reaction is advantageous for high yield production of proteins in different eukaryotic cell-free systems . One of the standardized vectors that can be used for CHO cell-free systems is the in vitro expression vector EasyXpress pIX3.0 (Biotechrabbit GmbH, Germany). The additional insertion of the intergenic region (IGR) IRES site of cricket paralysis virus (CRPV) into the pIX3.0 vector leads to high levels of cell-free produced protein in coupled batch based systems . To exploit the flexibility of our newly developed cell-free system, different plasmids, harboring CRPV and EMCV IRES site and a gene encoding firefly luciferase protein, were applied to translation reactions based on extracts from CHO cells. The first part of this study included cell-free synthesis based on different vector backbones such as pIX3.0-CRPV(GCT)-Luc, pcDNA3.1-CRPV(GCT)-Luc, pGem-EMCV-Luc and pT7CFE1-EMCV-Luc (Table 1). pIX3.0 and pT7CFE1 based vectors are currently used for cell-free synthesis in commercially available cell-free protein synthesis kits (Biotech Rabbit GmbH, Thermoscientific). Highest luciferase protein yields were detected by using an optimized pIX3.0-CRPV(GCT)-Luc template for cell-free protein synthesis (25.8 μg/ml radio labeled protein and 24.0 μg/ml active protein). Using other vector backbones, protein yields of approximately 1.1 to 4.5 μg/ml of radio labeled and 1.5 to 3 μg/ml of active protein yield could be reached (Fig 1A, Table 1). A direct comparison of IRES dependent protein production was performed using plasmids harboring the CRPV-IGR-IRES and EMCV-IRES. Our results show that higher luciferase yields could be obtained by using the CRPV-IGR-IRES site. We additionally examined the molecular weight of de novo synthesized luciferase proteins using standard western blot analysis. The results of the analysis are shown in Fig 1B. Luciferase protein bands could be detected in all of the different samples, whereas in the negativ control, which represents translation mixture without DNA template for monitoring the detection background of the synthesis reaction, no luciferase protein band could be detected. The intensity of protein bands differs, while samples including pIX3.0-CRPV(GCT)-Luc and pcDNA3.1-CRPV(GCT)-Luc DNA templates show the highest intensity.
A. Total protein yields were determined by incorporation of radioactive 14C leucine into de novo synthesized proteins followed by hot TCA precipitation and scintillation measurement. Yields of active luciferase were quantified by standard luciferase assay. B. Western blot analysis of cell-free produced luciferase using primary Anti-Luc antibody (concentration 1:1000) and secondary Anti-rabbit-HRP conjugate antibody (1:2000). Analysis of luciferase bands was performed by using ECL reagent and detection of corresponding light emission. Error bars show standard deviations calculated from triplicate analysis. NTC sample contains translation mixture without synthesized protein.
Optimization of cell-free reaction conditions
We performed a set of experiments to increase the total yield of cell-free synthesized luciferase using different DNA templates as described in part 3.1. Three individual experimental approaches were performed based on DNA template alterations. Initially, we have investigated the influence of various plasmid-DNA template concentrations in cell-free protein synthesis reactions for different templates (Fig 2A). The optimal DNA-concentration of pIX3.0-CRPV(GCT)-Luc used for in vitro translation in CHO cell lysates was determined to be approximately 50 ng/μl as also shown by Broedel et. al. . Different concentrations of DNA-templates were studied to examine the optimal value for each individual vector. In these initial experiments, we detected a decrease of active luciferase yield from 5 μg/ml to 3.9 μg/ml by increasing plasmid concentration of pIX3.0-EMCV-Luc (Fig 2A). However, by increasing the DNA concentrations of pT7CFE1-Luc in cell-free protein synthesis reactions from 50 ng/μl to 350 ng/μl, an increase of active protein concentration was detected, reaching the maximum protein yield at 250 ng/μl of DNA template. Using this DNA template concentration, protein yields of 7 μg/ml were reached which is 7 fold higher compared to start conditions. Further investigations included optimization of protein yield using a pcDNA3.1-CRPV(GCT)-Luc DNA template (Fig 2B). This plasmid is universally applicable as it can be used for cell-free protein synthesis as well as for cell-based protein production. The experimental setup was further expanded by analyzing different T7 RNA polymerase concentrations in coupled transcription/translation reactions. Different concentrations of T7 RNA polymerase were tested for pIX3.0-CRPV(GCT)-Luc DNA template. A saturation point of luciferase yield was obtained using 3 to 4 U/μl T7 RNA polymerase (S1 Fig). Therefore concentrations of 1 U/μl and 3 U/μl T7 RNA polymerase were tested for the different DNA templates. T7 RNA polymerase is a DNA dependent RNA polymerase which is commonly used in cell-free protein synthesis systems . So far, standard cell-free reactions based on CHO cell lysate, were conducted using 1 U/μl T7 RNA polymerase . In contrast, our results showed, that increased protein yields were reached by using 3 U/μl T7 polymerase and 150 ng/μl of pcDNA3.1-CRPV(GCT)-Luc DNA template. Comparison of the results of the two different tested T7 RNA polymerase concentrations showed significant improvement of protein yield using an increased concentration of 3 U/μl T7 RNA polymerase for cell-free protein synthesis (Fig 2B). This finding is also supported by the results depicted in Fig 2C. Efficient cell-free synthesis of erythropoietin (EPO) containing a melittin signal peptide is strongly dependent on T7 RNA polymerase concentration and plasmid DNA concentration. Cell-free synthesis was analyzed by synthesizing Mel-EPO. The highest protein yield was obtained by using 3 U/μl T7 polymerase and 50 ng/μl plasmid DNA. In the case of Mel-EPO, a slight decrease of protein yield could be detected by increasing plasmid concentration and T7 RNA polymerase. The supplementation of coupled transcription/ translation reactions with 3 U/μl T7 RNA polymerase (Stratagene) proved to be an efficient way to increase protein yields in CHO cell-free systems.
A. Analysis of plasmid concentration of pIX3.0-EMCV-Luc and pT7CFE1-Luc used for cell-free protein synthesis. Protein yields of active luciferase were determined by standard luciferase assay B. Dependence of protein yield on plasmid and T7 RNA polymerase concentration during cell-free synthesis based on the template pcDNA3.1-CRPV(GCT)-Luc. Protein yields of de novo synthesized luciferase were detected and calculated by quantification of 14C leucine labeled proteins and scintillation measurement. Luciferase assay was used for investigation of the amount of functional protein. Error bars represent standard deviations calculated from triplicate analysis. C Investigation of protein yield using pIX2.0-CRPV(GCT)-Mel-EPO DNA template. Variation of template DNA and T7 RNA polymerase concentration. Radio labeled proteins were analyzed by TCA precipitation followed by scintillation measurement (upper part C). Additionally, de novo synthesized proteins were visualized by autoradiography (lower part C).
To further analyze the effect of T7 RNA polymerase on the cell-free protein synthesis reactions, the initial optimization process was followed by experiments concerning the supplementation of molecular crowder macromolecule PEG to cell-free protein synthesis. It was reported that PEG components can impact mRNA folding  and can therefore decrease the dissociation rate of T7 RNA polymerase from mRNA molecules . Thus, we decided to evaluate the impact of different molecular size PEG molecules (PEG 3350, PEG 5000, PEG 20000) using two concentrations, 1% and 2%, in cell-free protein synthesis based on CHO cell lysate in the presence of 1U/μl T7 RNA polymerase (Fig 3). A reduction of T7 RNA polymerase is favorable to reduce the overall costs of the system, as supplementation costs for T7 RNA polymerase are approximately 25000 times higher compared to PEG addition. Therefore 1 U/μl T7 RNA polymerase was used during synthesis in the presence of PEG. A coupled transcription translation reaction was performed using pIX3.0-CRPV(GCT)-eYFP DNA template. The fluorescence signal of synthesized proteins was detected on μ-Ibidi slides (Fig 3A) and analyzed by Image Quant TL software quantification. The most intense fluorescence was observed adding 2% of PEG 5000, that was 2.5 and 1.8 fold higher compared to 1 U/μl and 3 U/μl T7 RNA polymerase controls, respectively (Fig 3B). A concentration dependent increase of the fluorescence signal was achieved using PEG 3350 and 5000 molecules. In the case of PEG 20000 an inhibitory effect to cell-free protein synthesis was detected for both tested concentrations. This effect was analyzed using different batches of lysate (S2 Fig). For all lysates an increase of protein yield could be detected by using PEG 3350 and PEG 5000 in comparison to 1 U/μl T7 RNA polymerase control.
Two concentrations (1%, 2%) of different PEG molecules (3350, 5000, 20000) were analyzed in cell-free protein synthesis reactions using pIX3.0-CRPV(GCT)-eYFP plasmid template. Translation reactions without the addition of PEG but with supplementation of 3 U/μl (increased concentration) and 1 U/μl (standard concentration) T7 RNA polymerase served as control reactions A. Fluorescence signals of synthesized eYFP proteins were detected by fluorescence imaging on μ-Ibidi slides using the Typhoon Trio Plus Imager. B. Quantification of fluorescence signals was accomplished by using Image Quant TL Array analysis software. Error bars show standard deviations calculated from triplicate analysis.
Cell-free synthesis of proteins using linear DNA templates
Besides the use of circular DNA templates, linear templates generated by PCR entail a high potential for easy and fast in vitro protein synthesis. During this study, linear DNA templates of luciferase and Mel-EPO, containing an CRPV-IRES and GCT as start codon, were generated by expression PCR and directly used for cell-free protein synthesis. Different concentrations of PCR product and T7 RNA polymerase were analyzed to obtain maximum protein yields. Basic conditions used for cell-free synthesis in Sf21 cell lysates were based on a final concentration of 7.5 ng/μl PCR product and 1 U/μl T7 RNA polymerase (Fig 4). An increase in protein yield was observed for both DNA constructs during stepwise enhancement of PCR product concentration. Increasing T7 RNA polymerase concentrations also led to a significantly improved protein synthesis (Fig 4). A plateau of protein yield could be detected by using 12.5 ng/μl and 15 ng/μl PCR product and 3 U/μl T7 RNA polymerase for both DNA templates. Maximum protein yields were obtained using 15 ng/μl PCR-product and 1 U/μl T7 RNA polymerase for linear IRES-luciferase DNA template and 15 ng/μl PCR-product and 3 U/μl T7 RNA polymerase for the linear IRES-Mel-EPO DNA template. An increase in T7 RNA polymerase concentration led to significantly higher proteins yields based on the IRES-Mel-EPO DNA template. In contrast, when using IRES-luciferase DNA template an increase of protein yield could only be obtained for PCR product concentrations of 7.5 ng/μl and 10 ng/μl. Using 12.5 ng/μl PCR product protein yield is not affected by T7 RNA polymerase concentration. Interestingly, a slight decrease of protein concentration could be detected in the sample containing 15 ng/μl PCR product upon increasing T7 RNA polymerase concentration (Fig 4).
Linear IRES-luciferase and IRES-Mel-EPO templates tested during cell-free protein synthesis reactions in the presence of 14C leucine. Different concentrations of linear DNA product and T7 RNA polymerase (Pol) were added to the individual reactions. Protein yield was quantified by hot TCA precipitation followed by scintillation measurement. Error bars show standard deviations calculated from triplicates.
Synthesis of different types of protein and accumulation of proteins in microsomal structures
To evaluate the performance of the CHO cell-free system, various so called “difficult-to-express” proteins were chosen for protein synthesis. Templates used in the cell-free system comprised the pH-gated potassium channel KcSA (KcsA), voltage-gated potassium uptake system KvaP (KvAP), transient receptor potential cation channel subfamily V member 1 (TRPV1), epidermal growth factor receptor (EGFR), potassium voltage-gated channel subfamily H member 2 (hERG), mu-type opioide receptor (OPMR1), channel rhodopsin-2 (ChRh2) and the beta-2 adrenergic receptor (B2AR). General characteristics of all produced proteins are illustrated in Table 2. Protein encoding DNA-fragments were integrated into pIX3.0 in vitro translation vector backbone harboring the CRPV-IRES at the 5´ UTR as well as the GCT start codon. For all proteins analyzed in the CHO cell-free system, the most prominent protein band of each sample corresponded to the expected molecular weight of the individual de novo synthesized protein (Fig 5). Analysis of KcsA, KvAP and ChRh2 revealed one additional protein band in each of the samples, indicating multimerisation of membrane proteins which was already demonstrated in the case of KcsA produced in a cell-free system based on Sf21 cell lysates . Tetramerisation is required to get functionally active KcsA . With respect to these results the second protein band that was detected in the KvAP and ChRh2 sample may give a hint of dimer formation of these proteins during the in vitro translation process. Initial results for functional analysis of the EGF receptor showed that proteins possess intrinsic kinase activity (S3 Fig). Autophosphorylation of EGFR at tyrosine residue could be detected by performing a kinase assay followed by immunoblotting. This result provides an initial indication for functional activity of “difficult-to-express” proteins synthesized in CHO cell-free system.
Standard cell-free protein synthesis was performed using pIX3.0-CPRV(GCT) plasmid backbones containing the different genes of interest. 14C leucine labeled proteins were precipitated in acetone, separated by SDS-PAGE and visualized by autoradiography. Produced proteins are listed in Table 2. Arrows indicate the expected protein band of each individual protein. No template control (NTC) contains translation mixture without template to visualize the background translational activity of the CHO lysate.
Previous studies in Sf21 cell lysates have shown cotranslational translocation of membrane proteins and posttranslationally modified proteins into endogenous microsomes of lysates . These microsomes are generated by a mild disruption procedure during cell lysate preparation. Brödel et. al. have reported that also CHO lysates contain addressable microsomes . Therefore multiple options to synthesize posttranslationally modified proteins and transmembraneous proteins are offered. Here we exemplarily demonstrate an enrichment of the glycoprotein Mel-EPO and the seven transmembrane receptor OPMR1 in microsomes of CHO cell lysates during the in vitro translation process. The experimental setup required a multiple addressing of the microsomal fraction by repetitive cycles of translation reaction with one batch of microsomes (Fig 6). This type of procedure was already demonstrated using the Sf21 cell-free protein synthesis system . Detailed analysis of the translation mixture, the supernatant after centrifugation and the microsomal fraction was performed after each cycle of microsome addressing. Synthesis levels of Mel-EPO and OPMR1 in the microsomal fraction shifted from 6 μg/ml (EPO) and 3.5 μg/ml (OPMR1) after the first cycle of cell-free translation to 12.5 μg/ml (EPO) and 7.5 μg/ml (OPMR1) after the third cycle. Only a slight increase of protein yields was observed when comparing cycle 2 and cycle 3 for both proteins. These results were confirmed by autoradiography (Fig 6). As expected, target proteins showed an apparent molecular mass of 21 kDa and 44 kDa in the SDS-PAGE gel (Fig 6). As expected, in vitro translation of Mel-EPO resulted in an additional protein band migrating around 25 kDa, which could only be detected in the translation mixture and the vesicular fraction, but not in the supernatant fraction. Analysis of repetitive OPMR1 synthesis revealed similar results. A protein band migrating at a slightly higher apparent molecular mass than expected was observed and the intensity of this band increased during the second repetitive cycle. With respect to these observations, we were able to show the enrichment of Mel-EPO and OPMR1 in microsomal fractions of CHO cell lysates and a significant increase in glycosylated protein.
During the first synthesis step (Cycle 1) Mel-EPO and OPMR1 protein was produced according to the optimized conditions (3 U/μl T7 RNA polymerase). After completing the cell-free reaction, translation mixture was separated into microsomal fraction and supernatant by centrifugation (15 min, 4°C and 16000xg) in a standard table top centrifuge. Supernatant was removed and microsomal fraction was resuspended using freshly prepared translation mixture containing CHO cell lysate without microsomal structures to initiate the second cell-free translation cycle (Cycle 2). This procedure was repeated again, after finishing the second translation step to obtain a third step of addressing the microsomal fraction (Cycle 3). Samples of translation mixture (TM), supernatant (S) and microsomal fraction (MF) were collected after each cycle for further analysis. Protein yields were quantified by hot TCA precipitation of 14C leucine labeled cell-free produced proteins followed by scintillation measurement. Error bars show standard deviations calculated from triplicate analysis. Molecular weight and modifications of proteins were visualized by SDS-PAGE separation and autoradiography.
Residue specific fluorescence labeling of proteins
In general, one of the advantages of cell-free protein synthesis is the open character of the system. Therefore, supplementation of non-canonical amino acids harboring fluorescence molecules or special sugar moieties becomes feasible. Incorporation of non canonical amino acids into protein structure was already presented for different types of cell-free protein synthesis systems including E. coli, wheat germ and Sf21 lysate based reactions [53–55]. In order to analyze the incorporation of non canonical amino acids using CHO lysates we supplemented BODIPY-TMR-Lysine-tRNA(Phe) to cell-free reactions. In theory, amino acid specific integration of BODIPY-TMR-tRNA at phenylalanine codons should result in efficient labeling of the cell-free synthesized proteins due to the high sensitivity of fluorescence probes [55,56]. This is a simple, feasible and alternative procedure to commonly used 14C leucine labeling of synthesized proteins. In this study we have analyzed fluorescence labeling of cell-free synthesized Mel-EPO and KcSA. Labeled proteins were analyzed by separation on SDS-PAGE gels followed by in-gel fluorescence analysis (Fig 7). For both synthesis reactions bands were detected at the expected molecular mass of the proteins in each fraction (translation mixture, supernatant, microsomal fraction). Labeling of Mel-EPO revealed the expected protein pattern of additional glycosylated proteins migrating at slightly higher molecular mass in the translation mixture as well as in the microsomal fraction. The tetrameric structure of fluorescently labeled KcSA was observed in the translation mixture and in the microsomal fraction exhibiting a molecular mass of around 54 kDa.
Cell-free protein synthesis based on CHO cell extracts was carried out in the presence of BODIPY-TMR-tRNA(Phe) to allow the fluorescence labeling of de novo synthesized Mel-EPO and KCSA. Produced glycosylated and transmembrane proteins were separated by SDS-PAGE. In-gel fluorescence was detected using a variable mode imager (Typhoon Trio Plus, GE Healthcare).
Discussion and Conclusion
Cell-free systems based on CHO cell lysates exhibit a tremendous potential for biotechnological applications in particular for the production of difficult-to-express proteins. The combination of well-known character and best-known safety aspects of CHO cells and the versatile cell-free technology bears many advantages for recombinant protein production.
In this study, we presented the potential of this platform with respect to different DNA templates, including various vector backbones as well as linear DNA templates, and further optimization strategies to increase the protein yield. Furthermore, we demonstrated the synthesis of different classes of proteins including ion channels, integral membrane protein receptors and G protein coupled receptors (GPCR).
Nowadays, a broad range of vector backbones are available that can be used for cell-free protein synthesis. Special requirements need to be fulfilled to enable a coupled transcription and translation reaction in cell-free systems. Commonly, transcription reactions are often conducted by using T7 RNA polymerase. Therefore the T7 promotor needs to be included in the 5´ UTR of the DNA template. Former studies revealed that cell-free systems based on CHO cell lysates showed most efficient translation rates by using an internal ribosomal entry site (IRES) in the 5´ UTR of the gene to be expressed . In this study, different IRES elements were tested for their performance. In this context, it was found that IRES secondary structures of the intergenic region (IGR) of the cricket paralysis virus (CRPV) resulted in highest protein yields in the CHO cell-free system  which are triggered by cap independent and initiation factor independent translation initiation mechanisms . By changing the start codon from ATG to GCT in the appropiate DNA template total protein yields were further increased . To show the flexibility of our CHO cell-free system, we tested different commercially available vector backbones suitable for cell-free and cell-based systems. We aimed to analyze the flexibility of template acceptance in the CHO cell-free system. All templates including an IRES could be used for cell-free protein synthesis. Significant differences of protein yields were detected comparing the optimized pIX3.0-CRPV(GCT)-Luc vector to other vector backbones (pcDNA3.1 (Thermoscientific), pGEM, pT7CFE1 (Thermoscientific)). In general, CRPV IRES plasmids pIX3.0-CRPV(GCT)-Luc and pcDNA3.1-CRPV(GCT)-Luc displayed increased protein yields in comparison to the pGEM-EMCV-Luc and pT7CFE1-EMCV-Luc plasmids that contained the encephalomyocarditis virus (EMCV) IRES. EMCV mediated translation initiation is not completely translation factor independent and requires the binding of eIF4G/4A complex, IRES trans-acting factor 45 (ITAF 45) and polypyrimidine tract binding protein (PBT) [58,59]. Increased protein yields of proteins synthesized from EMCV containing plasmids, compared to CRPV IRES containing plasmids, indicate that our CHO lysates might be limited in active factors essential for EMCV dependent translation initiation. Former studies reported dependence of EMCV IRES elements on Mg2+ ions . Thus, further optimization of salt concentrations including Mg2+ might consistently influence folding of the secondary structure of EMCV-IRES, enhance the stability of the initiation complex and thereby might increase protein production yields.
In this study, we additionally demonstrate the optimization of protein yields by adjusting plasmid and T7 RNA polymerase concentrations. So far, T7 RNA polymerase and pIX3.0 plasmid were applied in concentrations of 1U/μl and approximately 50 ng/μl, respectively, according to Broedel et. al. 2013. During the application of different vector backbones, it became obvious that plasmid concentrations needed to be adjusted in order to obtain the highest possible protein yields for each individual vector backbone. About 7 fold higher protein yields were obtained when using pT7CFE1-Luc and 250 ng/μl of DNA-template compared to standard conditions (50 ng/μl). Calculation of the molarity of different templates at maximum protein yields revealed a difference of optimum molarity (S1 Table). Initiation of transcription seems to be dependent on the structure of the individual DNA-template, a finding that is supported by previous studies . Increasing of the T7 RNA polymerase concentration from 1 U/μl to 3 U/μl led to significantly higher protein yields using various DNA constructs (pcDNA3.1-CRPV(GCT)-Luc and pIX2.0-CRPV(GCT)-Mel-EPO). This effect was even more significant than increasing template concentration. Althought the efficiency of T7 RNA polymerase based RNA transcription was obviously improved, production of glycosylated EPO was not significantly enhanced. This observation might be due to additional limitations affecting the translocation of EPO into the microsomal structures present in the lysate as a high yield of protein was detected in the supernatant fraction. High solubility of non-translocated protein offers a high potential for further translocation optimization. Raising T7 RNA polymerase concentrations might lead to an increased RNA production rate which might as a consequence results in higher protein yields. High concentrations of T7 RNA polymerase could also induce a molecular crowding effect, which is a common feature in living cells . It was shown before that T7 RNA polymerase and other macromolecules are positively affected by molecular crowding, thereby influencing biochemical kinetics by volume exclusion effects .
One of the commonly used molecular crowding reagents is poly ethylene glycol (PEG). The positive influence of PEG was demonstrated for E. coli and wheat germ based cell-free systems [64–67]. Our data indicate a positive molecular crowding effect in the CHO cell-free system. Upon application of PEG 3350 and PEG 5000 the fluorescence intensity of cell-free produced eYFP increased nearly 2-fold for each PEG concentration tested (1%, 2%) compare to standard conditions. Determined eYFP fluorescence intensity correlated with the total amount of de novo synthesized protein. Highest protein yields were obtained using 2% of PEG 5000. In contrast, PEG 20000 led to a significant decrease in protein yield. The high molecular weight PEG 20000 may affect the structure of endogenous proteins present in the lysate, thereby leading to protein precipitation  and subsequently to an inhibition of protein synthesis. Moreover, supplementation of PEG 3350 and PEG 5000 seems to be more efficient and also an economic way to increase protein yields in cell-free CHO systems compared to the cost-intensive increase of T7 RNA polymerase concentration from 1 U/μl to 3 U/μl.
Various automation strategies are currently in the focus of intense research activities pointing towards future applications of cell-free protein synthesis platforms. The need for novel high throughput protein synthesis strategies for the convenient preparation of “difficult-to-express” proteins, which are often targets for new pharmaceutical drugs, is obvious. Several automation strategies for cell-free systems have been published so far [55,69,70]. A cloning-free, fast and highly parallel synthesis of proteins can be achieved by using PCR products for cell-free protein synthesis. In this way, laborious cloning and vector design steps were circumvented . By using so called expression PCR, all necessary regulatory sequences, including promoter, terminator and IRES sites, are added to the individual target gene sequence  and the derived PCR product usally can be directly used for cell-free protein synthesis. We have demonstrated the suitability of linear DNA fragments generated by PCR for cell-free protein synthesis based on CHO cell lysate. Standard conditions specified for coupled Sf21 cell-free system (7.5 ng/μl PCR product (unpublished results)) revealed only low protein yields using the CHO based system. A significant increase (3–4.5 fold) of protein yield was detected by increasing PCR product concentration (Fig 4). Increase of T7 RNA polymerase only showed slight improvement of protein yield for the IRES Luc construct. On the other hand the effect on IRES-Mel-EPO was remarkable. Reasons for that might be the increased production of mRNA and molecular crowding effects, as described in the section above.
The developed cell-free system based on CHO cell lysate provides a solid basis and future potential for high throughput applications. As mentioned before, so called “difficult-to-express” proteins, e.g. a broad range of membrane proteins, constitute the largest class of potential drug targets . In this study, we have demonstrated the possibility to synthesize different classes of proteins in CHO cell-free system. First indications of ion channel multimerisation (KvAP and KcSA) and possible glycosylation of proteins (TRPV1, Mel-EGFR, OPMR1) were obtained. The potential to produce glycosylated EPO in CHO cell-free system was also demonstrated in former studies . Such posttranslational modifications and spatial arrangements of proteins are the basis to obtain a high portion of correctly folded and functionally active proteins. Enrichment of proteins in microsomal fractions by repetitive addressing, that was shown before for insect cell lysate based cell-free systems , could also be confirmed for CHO cell-free system, which is a precondition for increasing the amount of active luminal, transmembraneous and membrane attached proteins.
An alternative labeling method to the generally used radio labeling of cell-free synthesized proteins was demonstrated by using residue specific incorporation of BODIPY-TMR-LYS. Incorporation of this fluorescent amino acids enables a rapid and sensitive detection of proteins [36,56]. BODIPY-TMR coupled tRNA was successfully recognized by the ribosomal machinery of CHO cell lysate allowing the subsequent translocation of EPO and KcSA into microsomes and modifications of proteins including glycosylation and multimerisation. The possibility of cotranslational incorporation of fluorescence dyes during cell-free protein synthesis is a beneficial feature of this platform and provides opportunities for future applications, based on ultrafast and highly sensitive protein staining. This method is easily high throughput applicable and an alternative method, compared to radio labeling of proteins, for fast analysis. A new prospective could be created in the area of site directed labeling in CHO cell free system that allows for the specific integration of a non canonical amino acid at one desired position in the protein.
In conclusion, cell-free systems based on translationally active CHO cell lysates represent a promising platform for the synthesis of “difficult-to-express” proteins. The technology offers the possibility to synthesize proteins in an easy and rapid manner. The flexibility of DNA template usage offers an enormous potential for fast and easy template screening technologies. The mammalian origin of the system is highly beneficial for the production of a broad range of industrial target proteins. Furthermore, the open character of the system and the opportunity of automation and high throughput protein synthesis constitute a tool for simplification of future pharmaceutical pre-screening applications.
S1 Fig. Evaluation of T7 RNA polymerase concentration applied to cell-free protein synthesis.
Different concentrations of T7 polymerase (0.5 U/μ, 1U/μl, 2 U/μl, 3 U/μl, 4 U/μl) were supplemented to cell-free protein synthesis reactions. Protein yields of active luciferase were determined by standard luciferase assay.
S2 Fig. Influence of PEG addition to cell-free protein synthesis using different lots (1, 2, 3, 4) of CHO cell extract.
Different PEG molecules (3350, 5000) were added in two concentrations (1%, 2%) to cell-free protein synthesis reaction using pIX3.0-CRPV(GCT)-eYFP as a template. 3 U/μl (increased concentration) and 1 U/μl T7 RNA polymerase concentrations (standard concentration) were added to cell-free synthesis used as control reactions A. Fluorescence signals of synthesized eYFP proteins were detected by fluorescence imaging on μ-Ibidi slides using the Typhoon Trio Plus Imager (GE Healthcare). B. Quantification of fluorescence signals was accomplished by image analysis of μ-Ibidi slides by employing Image Quant TL Array Analysis software. Error bars show standard deviations that were calculated from triplicate analysis.
S3 Fig. In vitro phosphorylation of tyrosine residue 1068 in cell-free synthesized EGF receptor.
For analysis of autophosphorylation activity three samples were prepared containing an EGFR microsomal fraction, a no template control that consists of a microsomal fraction without synthesized protein and a microsomal fraction containing EGFR that is digested with calf intestinal phosphatase (CIP) after kinase buffer treatment. The CIP treated sample represents a specifity control for autophosphorylation. To allow for in vitro autophosphorylation of receptors embedded in the CHO microsomal membranes, microsomal fractions pelleted from 10 μl of the complete reaction mixture by centrifugation (15 min, 4°C, 16000xg) were collected and resuspended in 20 μl kinase buffer composed of 100 mM HEPES (pH 7.4), 1% glycerol, 0.1 mg/ml BSA, 5 mM MgCl2, 1.25 mM MnCl2, 0.1 mM NaVO3, 2 μM caspase inhibitor and 200 μM ATP. Incubation was carried out for 30 minutes at room temperature. Kinase reaction was followed by immunoblotting using the “IBlot Gel Transfer Device” (Life Technologies) according to the manufacturer’s instructions. Proteins were transferred from a 10% Bis-Tris SDS-PAGE (Life Technologies) to a PVDF membrane (Life Technologies). The membrane was blocked in TBS/T + 1% BSA for 4 hours and subsequently incubated with “Phospho-EGF Receptor (Tyr1068) (D7A5) XP® Rabbit mAb 3777” primary antibody diluted 1:1000 overnight at 4°C. “Anti-rabbit IgG, HRP-linked Antibody 7074” diluted 1:2000 was used as a secondary antibody and detection was carried out using the “Amersham ECL Prime Western Blotting Detection Reagent” (GE Healthcare) and the “Typhoon Trio+ Variable Mode Imager” (GE Healthcare).
- Conceptualization: LT DAW MS AS SK.
- Data curation: LT DAW SK.
- Formal analysis: LT MB.
- Funding acquisition: SK.
- Investigation: LT MB.
- Methodology: LT DAW MB MS AS SK.
- Project administration: LT SK.
- Resources: LT AS SK.
- Supervision: LT SK.
- Validation: LT DAW MB.
- Visualization: LT.
- Writing – original draft: LT MS SK.
- Writing – review & editing: LT DAW MS SK.
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