The MultiBac Protein Complex Production Platform at the EMBL

Summary

Protein complexes catalyze key cellular functions. Detailed functional and structural characterization of many essential complexes requires recombinant production. MultiBac is a baculovirus/insect cell system particularly tailored for expressing eukaryotic proteins and their complexes. MultiBac was implemented as an open-access platform, and standard operating procedures developed to maximize its utility.

Abstract

Proteomics research revealed the impressive complexity of eukaryotic proteomes in unprecedented detail. It is now a commonly accepted notion that proteins in cells mostly exist not as isolated entities but exert their biological activity in association with many other proteins, in humans ten or more, forming assembly lines in the cell for most if not all vital functions.^1,2 Knowledge of the function and architecture of these multiprotein assemblies requires their provision in superior quality and sufficient quantity for detailed analysis. The paucity of many protein complexes in cells, in particular in eukaryotes, prohibits their extraction from native sources, and necessitates recombinant production. The baculovirus expression vector system (BEVS) has proven to be particularly useful for producing eukaryotic proteins, the activity of which often relies on post-translational processing that other commonly used expression systems often cannot support.³ BEVS use a recombinant baculovirus into which the gene of interest was inserted to infect insect cell cultures which in turn produce the protein of choice. MultiBac is a BEVS that has been particularly tailored for the production of eukaryotic protein complexes that contain many subunits.⁴ A vital prerequisite for efficient production of proteins and their complexes are robust protocols for all steps involved in an expression experiment that ideally can be implemented as standard operating procedures (SOPs) and followed also by non-specialist users with comparative ease. The MultiBac platform at the European Molecular Biology Laboratory (EMBL) uses SOPs for all steps involved in a multiprotein complex expression experiment, starting from insertion of the genes into an engineered baculoviral genome optimized for heterologous protein production properties to small-scale analysis of the protein specimens produced.^5-8 The platform is installed in an open-access mode at EMBL Grenoble and has supported many scientists from academia and industry to accelerate protein complex research projects.

Introduction

Biological activity is controlled by assemblies of proteins and other biomolecules that act in concert to catalyze cellular functions. Notable examples include the machinery that transcribes the hereditary information contained in DNA into messenger RNA. In humans, more than 100 proteins come together in a defined and regulated process to transcribe genes, forming large multiprotein complexes with 10 and more subunits including RNA polymerase II and the general transcription factors such as TFIID, TFIIH and others.⁹ Other examples are the ribosome, consisting of many proteins and RNA molecules, that catalyzes protein synthesis, or the nuclear pore complex which is responsible for shuttling biomolecules through the nuclear envelope in eukaryotes. A detailed architectural and biochemical dissection of essentially all multicomponent machines in the cell is vital to understand their function. The structure elucidation of prokaryotic and eukaryotic ribosomes, for instance, constituted hallmark events yielding unprecedented insight into how these macromolecular machines carry out their designated functions in the cell.^10,11

Ribosomes can be obtained in sufficient quality and quantity for detailed study by purifying the endogenous material from cultured cells, due to the fact that up to 30% of the cellular mass consists of ribosomes. RNA polymerase II is already less abundant by orders of magnitude, and many thousand liters of yeast culture had to be processed to obtain a detailed atomic view of this essential complex central to transcription.¹² The overwhelming majority of the other essential complexes are however present in much lower amounts in native cells, and thus cannot be purified adequately from native source material. To render such complexes accessible to detailed structural and functional analysis requires heterologous production by using recombinant techniques.

Recombinant protein production had a major impact on life science research. Many proteins were produced recombinantly, and their structure and function dissected at high resolution. Structural genomics programs have taken advantage of the elucidation of the genomes of many organisms to address the gene product repertoire of entire organisms in high-throughput (HT) mode. Thousands of protein structures have thus been determined. To date, the most prolifically used system for recombinant protein production has been E. coli, and many expression systems have been developed and refined over the years for heterologous production in this host. The plasmids harboring a plethora of functionalities to enable protein production in E. coli fill entire catalogues of commercial providers.

However, E. coli has certain limitations which make it unsuitable to produce many eukaryotic proteins and in particular protein complexes with many subunits. Therefore, protein production in eukaryotic hosts has become increasingly the method of choice in recent years. A particularly well-suited system to produce eukaryotic proteins is the baculovirus expression vector system (BEVS) that relies on a recombinant baculovirus carrying the heterologous genes to infect insect cell cultures cultivated in the laboratory. The MultiBac system is a more recently developed BEVS which is particularly tailored for the production of eukaryotic protein complexes with many subunits (Figure 1). MultiBac was first introduced in 2004.¹³ Since its introduction, MultiBac has been continuously refined and stream-lined to simplify handling, improve target protein quality and generally making the system accessible to non-specialist users by designing efficient standard operating procedures (SOPs).⁴ MultiBac has been implemented in many laboratories world-wide, in academia and industry. At the EMBL in Grenoble, transnational access programs were put in place by the European Commission to provide expert training at the MultiBac platform for scientists who wished to use this production system for advancing their research. The structure and function of many protein complexes that were hitherto not accessible was elucidated by using samples produced with MultiBac.⁴ In the following, the essential steps of MultiBac production are summarized in protocols as they are in operation at the MultiBac facility at EMBL Grenoble.

Protocol

1. Tandem Recombineering (TR) for Creating Multigene Expression Constructs

1. Planning the co-expression strategy. Design approach for inserting your genes of interest into Donors and Acceptors. Potential physiological submodules of your complex should be grouped together on specific Acceptors and Donors. Use Multiplication Module consisting of Homing endonuclease (HE) - BstXI pairs to combine expression cassettes on individual Donor and Acceptor plasmids.^7,8 Create all relevant constructs in silico and validate strategy thoroughly before proceeding to experimental work. For example, genes of interest should be checked not to contain HE or other restriction sites and the presence of correct open reading frames (ORFs) should be validated. Consider ordering synthetic genes optimized for insect cell codon usage and mRNA secondary structure to improve protein production levels as well as removal of any existing HE sites from the genes of interest. Consider placing purification tags based on data from the literature about flexible or exposed N- or C-termini of your proteins of choice. Consider applying polyprotein strategies that aim at producing several protein subunits in your complex if the relative amounts of individual proteins need to be controlled due to stoichiometry issues in the complex.⁴ Prepare detailed "How-To" document (electronic lab book is recommended) containing all projected experimental steps of the project leading up to the complete multigene construct(s). Create electronic files of the Cre-LoxP fused plasmids for example by using the Cre-ACEMBLER software which can be downloaded from the Berger group home page (www.embl.fr/multibac/ multiexpression_technologies/cre-acembler).
2. Insert your genes of interest into selected Donors and Acceptors by using restriction enzymes and ligase, or, alternatively, by using ligation independent methods following published protocols.^5,6,14 If you have access to a liquid handling work-station and if you plan a large number of constructs to be generated (for example for combinatorial approaches) consider using robotics scripts developed and implemented by the Berger group (Figure 2).^14,15 If a liquid handling work-station is not available, manual operation using microtitre plates allows gene insertion in a HT like fashion.
3. Constraints imposed by the need to control the stoichiometry of the expressed subunits may materialize. In the case of stoichiometrically imbalanced expression levels of individual subunits of a protein complex, consider applying polyprotein strategies to conjoin several subunits of your complex and a specific protease (for example tobacco etch virus NIa protease) in single large ORFs spaced by specific proteolytic sites.^4,8 Consider co-expressing one or several polyproteins with single expression cassettes if you have a very large complex with many subunits and widely ranging molecular weights of individual subunits. Consider co-expressing several genes encoding for the same protein in a polyprotein or as several identical expression cassettes if that protein is characterized by low production yield.^4,13
4. Validate all Donor and Acceptor constructs cloned by restriction mapping (optionally in high-throughput) and sequencing. Proceed to fuse Donor-Acceptor combinations by Cre-LoxP recombination to generate the multigene expression constructs of choice. Validate purified Acceptor-Donor fusion plasmids by restriction mapping, use electronic sequences created by Cre-ACEMBLER or similar programs as a reference.
5. Store purified and validated Donors, Acceptors and Donor-Acceptor fusions at -20 °C or -80 °C. Archive plasmids and their sequences (Microsoft Excel, Filemaker, others) carefully for later usage.

2. Composite Multigene Baculovirus Generation, Amplification and Storage

1. Integrate multigene transfer vectors the MultiBac baculoviral genome by transforming into DH10 cells harboring the viral genome and the functionalities required for Tn7 transposition. Note that the Multibac baculoviral genome can be preloaded with particular genes of interest (YFP marker, chaperones, etc.) in its own LoxP site (engineered into the genome distal to the Tn7 attachment site) by an in vivo Cre reaction preceding Tn7 integration.¹³ After Tn7 transposition, cells with composite baculovirus containing the genes of interest are selected by blue/white screening (successful Tn7 transposition results in loss of α-complementation of the β-galactosidase; therefore, colonies with correct Tn7 transposition remain white on selective agar plates containing X-gal) and the genome is prepared by alkaline lysis and ethanol/isopropanol precipitation.^5,6
2. Transfection and initial virus production. Place 6-well tissue culture plate into sterile hood. From log-phase Sf21 insect cell culture, seed out aliquots of cells in the wells and transfect by adding the purified baculoviral genome and a transfection reagent mixed in culture media as described.⁶ Harvest initial virus after 48-60 hr by removing the media (high quality, low titer virus V₀, typically 3 ml per well). Supplement fresh media, and test for protein production (and, if a YFP marker is present, for fluorescence) after an additional 2-3 days.^6,7
3. Amplification of virus, low MOI regimen. Use V₀ virus to infect 25-50 ml of cells in log phase (cell density <1x10⁶ cells per ml) in small (100-250 ml) Erlenmeyer shaker flasks agitated on orbital platform shakers (Figure 3). Count cells and split every 24 hr until cells stop doubling (proliferation arrest). Follow a low MOI (multiplicity of infection i.e. number of virus particles per cell) regimen: Cells must double (at least) once (MOI < 1), otherwise repeat experiment with a smaller volume of V₀ added. Normally, 3 ml of V₀ are used to infect 25 ml of Sf21 insect cells at a density of 0.5x10⁶ cells / ml. This is essential to prevent detrimental over-amplification and auto-deletion of virus that can result in loss of the heterologous genes of interest. Harvest V₁ virus (25-50 ml) after 48-60 hr by pelleting cells and removing the media containing the virus. Supplement with fresh media and test for YFP and protein production by removing 1x10⁶ cells every 12 or 24 hr, pelleting and validating protein production and marker protein (YFP) signal.⁶, Amplify virus (to V₂) further if larger expression volumes are aimed at by infecting up to 400 ml cells in 2 L shaker flasks with V₁ virus respecting the above low MOI regimen (cells must double at least once after infection with V₁). Stringently test protein production and marker protein signal during amplification to avoid accumulation of defective viruses no longer containing your genes of interest.^5-7 Use cell pellets accumulating at each amplifications step already for establishing purification protocols for the expressed protein complex of interest.
4. BIIC storage of production virus. We strongly recommend to store V₂ virus as the production virus by using the BIIC (Baculovirus-infected insect cells) method, to prevent modifications (e.g. loss of the gene of interest) of the recombinant virus and to preserve high expression levels.¹⁶ Pellet infected cells 24 hr after proliferation arrest is observed - at this stage cells contain complete viral particles just before they would be released (by budding) into the media. Remove media and freeze aliquots of the cell pellet in liquid nitrogen and store indefinitely.^7,16

3. Protein Production and Downstream Processing

1. Infecting large(r) cultures and monitoring YFP. Use V₁, V₂ or frozen BIIC aliquots to infect larger cell cultures for production runs (typically 400 ml in 2 L flasks). Adhere to low MOI regimen (adjust virus volume used for infection such that infected culture doubles at least once). Enlarge infected culture volumes if needed by multiplying number of flasks. If YFP marker protein is present, withdraw at defined intervals 1x10⁶ cells, pellet and lyse cells and monitor evolution of the YFP signal until a plateau is reached indicating maximum recombinant protein production. YFP levels can be measured in a standard 96 well plate reader capable of recording fluorescence signals (e.g. Tecan SPECTRAFluor). Harvest cells at this stage. Store cell pellets at -20 °C (short term) or -80 °C (long term).
2. Cell lysis and fractionation. Lyse cells by your favorite method of choice, tailored to the requirements of your protein (freeze-thaw, sonication, French press, others).^5-7 Fractionate cytosol and nuclei and test for the presence of your proteins of interest. Develop purification protocols based on the results to simplify protein purification. Consider applying soaking procedures to extract your protein from the nuclear fraction under high KCl conditions if your proteins reside in the nucleus.^7,18
3. Protein purification (micro-scale, large scale). Note that often small volumes (10 or 25 ml) of cell culture are sufficient for obtaining cell pellets for purifying substantial amounts of your proteins of interest due to the typically high or very high production levels of heterologous proteins in the baculovirus/insect cell systems (often 10-100 mg of protein per L culture and more). In conjunction with micro-purification (multiwell plates, microtip methods, GE Healthcare ÄKTAmicro system, others) it is possible to obtain biochemical and activity data and often also sufficient amount of the desired proteins and complexes for nanoliter-scale high-throughput crystallization (HTX). Consider using metal affinity purification (Clonetech Takara TALON, Qiagen NiNTA metal chelator resins) and an oligo-histidine (6-10 residues) tag on exposed subunits of your protein complex to facilitate purification, in conjunction with ion exchange and size exclusion chromatography in small volumes using for example the ÄKTAmicro or a similar small volume purification machine (Figure 4). Other affinity purification steps and ion exchange (IEX) steps in addition to the affinity purification with oligo-histidine tags or other tags (choose from GST, MBP, CBP, others) can and should be considered, according to the biochemical properties of the proteins of interest and individual preferences. Consider tagging more than one subunit with affinity tags to enhance purification efficiency. Concentrate your purified protein complexes and establish storage protocols such as freezing with or without glycerol. Develop quality control criteria that can be applied standardly (activity assays, biochemical and biophysical tests) to assess batch-to-batch variation of your purified proteins.

Results

Strong co-expression of heterologous proteins achieved by the MultiBac system is shown in Figure 1d (probes taken 48 hr after infecting a suspension cell culture). The overexpressed protein bands are clearly discernible in the whole cell extract (SNP) and the cleared lysate (SN). The quality and quantity of the protein material produced is often sufficient to enable structure determination of protein complexes, such as the mitotic checkpoint complex MCC shown in Figure 1e.¹⁷

Discussion

Video snap-shots in Figures 2 and 3 illustrate the entire process from robot-assisted generation from cDNA of multigene expression constructs all the way to infection of insect cell cultures for protein production. New reagents (plasmids and virus) and robust protocols have been developed to enable a pipeline relying on SOPs. The entire pipeline has been implemented as a platform technology at the EMBL in Grenoble. The MultiBac platform has been accessed by many scientists from academia ...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Bluo-Gal	Invitrogen	15519-028 (1 g)
Tetracycline	Euromedex	UT2965-B (25 g)	1,000X at 10 mg/ml
Kanamycine	Euromedex	EU0420 (25 g)	1,000X at 50 mg/ml
Gentamycine	SIGMA	G3632 (5 g)	1,000X at 10 mg/ml
IPTG	Euromedex	EU0008-B (5 g)	1,000X at 1M
Cre-recombinase	New England BioLabs	M0298
X-Treme GENE HP transfection reagent	Roche	06 366 236 001
Hyclone SFM4 Insect	Thermo Scientific	SH 30913.02
6-well plate Falcon	Dominique Dutscher	353046
2 ml pipette Falcon	Dominique Dutscher	357507
5 ml pipette Falcon	Dominique Dutscher	357543
10 ml pipette Falcon	Dominique Dutscher	357551
25 ml pipette Falcon	Dominique Dutscher	357535
50 ml pipette Falcon	Dominique Dutscher	357550
50 ml tube Falcon	Dominique Dutscher	352070
15 ml tube Falcon	Dominique Dutscher	352096
1.8 ml cryotube Nunc	Dominique Dutscher	55005
100 ml shaker flasks Pyrex	Dominique Dutscher	211917
250 ml shaker flasks Pyrex	Dominique Dutscher	211918
500 ml shaker flasks Pyrex	Dominique Dutscher	211919
2 L shaker flasks Pyrex	Dominique Dutscher	211921
Certomat Orbital Shaker + plateau	Sartorius	4445110, 4445233
Liquid nitrogen tank dewar 35 L	Fisher Scientific	M76801
Biological Safety Cabinet Faster	Sodipro	FASV20000606
Optical Microscope	Zeiss	451207
Sf21 Insect cells
Hi5 Insect cells	Invitrogen	B855-02
Tecan freedom EVO running Evoware plus	TECAN
10 μl conductive tips (black),	TECAN	10 612 516
200 μl conductive tips (black)	TECAN	10 612 510
disposable trough for reagents, 100 ml	TECAN	10 613 049
twin.tec PCR plate 96, skirted	Eppendorf	0030 128.648
96 well V bottom, non sterile	BD falcon	353263
96 deepwell plate color natural, PP)	Fisher	M3752M
PS microplate, 96 well flat bottom	Greiner	655101
96 deepwell plate	Thermo scientific	AB-0932
24 well blocks RB	Qiagen	19583
DpnI restriction enzyme	NEB	R0176L	20 U/uL
NEBuffer 4 10X	NEB	B7004S
2X phusion mastermix HF	Finnzyme	ref F-531L
2X phusion mastermix GC	Finnzyme	ref F-532L
DGLB 1.5X	homemade		7.5% glycerol, 0.031% Bromophenol blue, 0.031% Xylen cyanol FF
High DNA Mass Ladder for e-gel	Life Technologies	10496-016
Low DNA Mass Ladder for e-gel	Life Technologies	10068-013
E-gel 48 1% agarose GP	Life Technologies	G8008-01
Nucleo Spin- robot-96 plasmid kit	Macherey Nagel	740 708.24
PCR clean-up kit, Nucleospin Robot-96 Extract	Macherey Nagel	740 707.2
Gotaq green master mix	Promega	M7113
T4 DNA polymerase, LIC-qualified	Novagen	70099-3
DTT 100 mM	homemade
Urea 2 M	homemade
EDTA 500 mM pH 8.0	Homemade
LB broth (Miller) 500 g	Athena ES	103