Method Article

Modifying Baculovirus Expression Vectors to Produce Secreted Plant Proteins in Insect Cells

DOI:

10.3791/58283

August 20th, 2018

In This Article

Summary

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Here, we present the protocols for utilizing the insect cell and baculovirus protein expression system to produce large quantities of plant secreted proteins for protein crystallization. A baculovirus expression vector has been modified with either GP67 or insect hemolin signal peptide for plant protein secretion expression in insect cells.

Abstract

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It has been a challenge for scientists to express recombinant secretory eukaryotic proteins for structural and biochemical studies. The baculovirus-mediated insect cell expression system is one of the systems used to express recombinant eukaryotic secretory proteins with some post-translational modifications. The secretory proteins need to be routed through the secretory pathways for protein glycosylation, disulfide bonds formation, and other post-translational modifications. To improve the existing insect cell expression of secretory plant proteins, a baculovirus expression vector is modified by the addition of either a GP67 or a hemolin signal peptide sequence between the promoter and multiple-cloning sites. This newly designed modified vector system successfully produced a high yield of soluble recombinant secreted plant receptor proteins of Arabidopsis thaliana. Two of the expressed plant proteins, the extracellular domains of Arabidopsis TDR and PRK3 plasma membrane receptors, were crystallized for X-ray crystallographic studies. The modified vector system is an improved tool that can potentially be used for the expression of recombinant secretory proteins in the animal kingdom as well.

Introduction

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It is imperative for a research laboratory to be capable of producing large quantities of homogeneous recombinant proteins for biochemical and biophysical characterizations, especially for X-ray crystallographic studies. There are many well-established heterologous expression systems such as Escherichia coli, yeast, insect cells, mammalian cells, plant cells, etc. Among them, the baculovirus-mediated insect cell expression system is one of the most commonly used techniques to produce large quantities of structurally folded large-sized recombinant eukaryotic proteins for protein crystallization1.

The....

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Protocol

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NOTE: An insect cell/baculovirus system with modified expression vectors for secretory plant protein expression and crystallization is used.

1. Modification of a Baculovirus Expression Vector with the GP67 Signal Peptide for Plant Protein Secretion Expression

  1. Synthesize a DNA fragment containing a 5' BglII cutting site13, the GP67 secretion signal sequence, and a multi-cloning site with NotI, BamHI, EcoRI, StuI, SalI, SpeI, XbaI, PstI, and XhoI (Figure 1A).
    NOTE: Since both BglII and BamHI digested DNA resulted in the same adhesive ends, the linearized vector can l....

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Results

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As shown in Figure 1, two modified pFastBac1 baculovirus expression vectors were used to express the secreted proteins with either the GP67 or the hemolin signal sequence to replace the intrinsic signal sequence of the target gene. The viral GP67 and the insect hemolin genes have been demonstrated to have high secretion expression levels in the cells. Fusion proteins with either of these two signal sequences are expected to have greatly improved secretion exp.......

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Discussion

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Given the diversity in size and stability of the thousands of proteins present in the biological systems, it is often empirical for a research laboratory to decide which heterologous expression system has to be chosen for the expression of a specific protein. The E. coli expression system is often the first choice for protein expression due to the short life cycle of the bacteria, low cost of the culture media, and relative ease to scale up19. For the expression of large eukaryotic protei.......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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This work was supported by the new faculty startup funds from North Carolina State University for Guozhou Xu.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Incubator shakerVWRModel Excella E2527 oC
IncubatorVWRModel 200527 oC
CentrifugeBECKMANModel J-6with a swing bucket rotor
Herculase II Fusion DNA PolymeraseAgilent600677-51For PCR amplification of DNA
Thermal CyclerBIO-RADModel C1000 TouchFor PCR amplification of DNA
Incubator shakerNew Brunswick ScientificModel I 24For growing baceria culture
Customer DNA synthesisGENSCRIPT
BamHI (HF)New England BiolabsR3136SRestriction Endonuclease
BglIINew England BiolabsR0144SRestriction Endonuclease
NotI (HF)New England BiolabsR3189SRestriction Endonuclease
XhoINew England BiolabsR0146SRestriction Endonuclease
T4 DNA ligaseNew England BiolabsM0202TDNA ligation
QIAquick Gel Extraction KitQiagen28704DNA purification from Agorase gel
QIAprep Spin Miniprep KitQiagen27104Plasmid DNA purification from bacteria culture
AgaroseThermo Fisher Scientific15510-019For DNA gel electropherosis
MAX Efficiency DH5α competen cellInvitrogen18-258-012For transformation of DNA ligation mixture
Lennox L LB BrothResearch Product International Corp.L24066-5000.0For making bacteria culture
Ampicillin sodium saltThermo Fisher Scientific11593-019Antibiotics
Kanamycin SulfateThermo Fisher Scientific15160-054Antibiotics
TetracyclineThermo Fisher Scientific64-75-5Antibiotics
GentamicinThermo Fisher Scientific15710-064Antibiotics
MAX Efficiency DH10Bac competent cellsThermo Fisher Scientific10361-012For making bacmid DNA
S.O.C. MediumThermo Fisher Scientific15544-034For DNA transformation
CellFECTIN II ReagentThermo Fisher Scientific10362-101Insect cell transfection reagent
Bac-to-Bac Expression SystemThermo Fisher Scientific10359-016Baculovirus-insect cells expression kit
Bluo-galThermo Fisher Scientific15519-028For isolation of recominant Bacmid DNA
IPTGThermo Fisher Scientific15529-019For isolation of recominant Bacmid DNA
pFastBac1Thermo Fisher Scientific10360014Baculorirus expression vector
Sf9 cellsThermo Fisher Scientific11496015Sf9 monolayer cells
Hi5 cellsThermo Fisher ScientificB85502High Five insect cells
Grace’s insect medium, unsupplementedThermo Fisher Scientific11595030Sf9 cell transfection minimum medium
Grace’s insect medium, supplementedThermo Fisher Scientific11605102Sf9 monolayer cell culture complete medium
Sf-900 II SFMThermo Fisher Scientific10902104Sf9 suspension cell culture medium without FBS
Express Five SFMThermo Fisher Scientific10486025Hi5 cell culture medium
Penicillin-StreptomycinThermo Fisher Scientific15140122100 ml (10,000 I.U./ml)
L-Glutamine (200 mM)Thermo Fisher Scientific25030081100 ml
FBS CertifiedThermo Fisher Scientific16000-044500 ml
6-well platesThermo Fisher Scientific08-772-1BFlat-bottom
150 mm platesThermo Fisher Scientific353025100/case
1.5 ml Microcentrifuge TubesUSA Scientific1415-2500500 tubes/bag
15 ml conical screw cap centrifuge tubesUSA Scientific1475-051125 tubes/bag
50 ml conical screw cap centrifuge tubesUSA Scientific1500-121125 tubes/bag
Ni-NTA SuperflowQiagen30430NiNTA resin
pH-indicator stripsEMD Millipore Corporation1.09535.0001pH 0 - 14

References

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  1. Contreras-Gomez, A., Sanchez-Miron, A., Garcia-Camacho, F., Molina-Grima, E., Chisti, Y. Protein production using the baculovirus-insect cell expression system. Biotechnology Progress. 30, 1-18 (2014).
  2. Khan, S., Ng, M. L., Tan, Y. J.

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Tags

Insect Cell ExpressionSignal Peptide SequencesProtein PurificationX ray CrystallographyCryo EM AnalysisSf9 Cell CultureBacmid DNA PreparationRecombinant Virus Amplification

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