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1 Expression in Eukaryotic Systems • Yeast - Saccharomyces cerevisiae (baker’s yeast) - Pichia pastoris Insect Cells – Baculovirus Mammalian Cells

1 Expression in Eukaryotic Systems Yeast - Saccharomyces cerevisiae (baker’s yeast) - Pichia pastoris Insect Cells – Baculovirus Mammalian Cells

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Page 1: 1 Expression in Eukaryotic Systems Yeast - Saccharomyces cerevisiae (baker’s yeast) - Pichia pastoris Insect Cells – Baculovirus Mammalian Cells

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Expression in Eukaryotic Systems

• Yeast

- Saccharomyces cerevisiae (baker’s yeast) - Pichia pastoris

• Insect Cells – Baculovirus

• Mammalian Cells

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Expression in Yeast

Autonomous replicating vectors -> shuttle vectors

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Expression in Saccharomyces cerevisiaeAutonomous replicating systems

Yep

Yrp

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Expression in Saccharomyces cerevisiaeIntegrative systems

Probability for integration higher with linear fragments !

YIp

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Yeast Artifical Chromosomes

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Yeast Artifical Chromosomes (YAC)

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Expression in Saccharomyces cerevisiae

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Yeast Promoter

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UAS: Upstream activating sequenceURS: Upstream repressing sequence

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Expression in Saccharomyces cerevisiae

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Expression in Saccharomyces cerevisiae

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Yeast are efficient secretors !

Secretory expression preferred if:

-> if product toxic

-> if many S-S bonds need to be closed

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Expression in S. cerevisiae – Pichia pastoris

Problems with production in S. cerevisiae:

• For some proteins production level low• Hyperglycosylation (more than 100 mannose residues in N-glycosylation)• Sometimes secretion not good -> protein stack in cells (periplasma)• S. cerevisiae produces high amount of EtOH -> toxic for the cells -> effects

level of production

Advantages of production in Pichia pastoris:

• Highly efficient promoter, tightly regulated (alcohol oxidase -> AOX, induced by MeOH)

• Produces no EtOH -> very high cell density -> secretion very efficient• Secretes very few proteins -> simplification of purification of secreted

proteins

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Expression in Pichia pastorisIntegrative systems

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Expression in Pichia pastoris

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Expression in Pichia pastoris

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Expression in Pichia pastoris

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Mut+ -> both AOX1 and AOX2 are functional -> methanol as inducer and as carbon source used

MutS -> only AOX2 functional -> methanol as inducer and just to minder extend as carbon sourse

Mut- -> non of the AOX are functional -> methanol only as inducer

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”Knockout” strains (Lab strain design)

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Glycosylation

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Expression in Pichia pastoris

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Yeast surface display

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Yeast Two-Hybrid System

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-> to study protein-protein interactions

-> another possibility by SPR

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Expression in Insect cells

• Baculovirus:-> infects invertebrates (insects)-> in infection cycle 2 forms of baculovirus are formed: -> single virus particle -> in protein matrix (polyhedron) trapped clusters of viruses

-> during late stage of infection massive amount of polyhedron produced -> strong promoter

-> polyhedron not required for virus production-> polyhedron promoter optimal for heterologous protein production in insect cells

-> Autographa californica multiple nuclear polyhedrosis virus (AcMNPV) often used as expression vector

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Baculovirus expression system

-> Production of recombinant baculovirus: 1. create a transfer vector (E. coli based plasmid with AcMNPV DNA – polyhedrin promoter/terminator + flanking sequences) -> gene of interest cloned downstream of promoter

2. Insect cells are cotransfected with virus (AcMNPV) + transfer vector -> in some double infected cells -> double crossover event (recombination) -> produce recombinant virus (bacmid -> E. coli - insect cell baculovirus shuttle vector)

-> cells infected with recombinant virus -> produce plaques (lack of polyhedrin)

3. DNA hydridisation + PCR used to identify recombinant virus

4. Infection of insect cells with concentrated stock of verified recombinant virus -> 4-5 days later protein harvested

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Baculovirus expression system

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Why this system?

1. Insect cells have almost the same posttranslational modifications as mammalian cells

2. Higher expression level than mammalian cells

Baculovirus expression system

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Drosophila cells as expression system

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Drosophila cells as expression system

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Drosophila cells as expression system

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Mammalian cell expression system

1. Why do we use that system? -> to get full complement of posttranslational modifications on proteins

2. Developed cell lines: -> short term (transient) expression -> autonomous replicating systems -> viral

origins (SV40) - African green monkey kidney (COS) - baby hamster kidney (BHK) - human embryonic kidney (HEK-239)

-> long term (stable) expression -> integration into chromosome -> viral origins - chinese hamster ovary (CHO)

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Mammalian cell expression system

1. Adenoviral Vector

2. Cytomegalovirus (CMV) promoter

3. Inducible mammalian expression systems

4. Sindbis Virus

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Adenoviral expression system

-> used for gene therapy !!!

Many cell types can be infected !!!

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Adenoviral expression system

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Adenoviral expression system

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Cytomegalovirus enhancer-containing promoter

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Cytomegalovirus enhancer-containing promoter

-> positive and negative regulation of promoter

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Cytomegalovirus enhancer-containing promoter

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Inducible Mammalian Expression Systems

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Inducible Mammalian Expression Systems

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Inducible Mammalian Expression Systems

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Inducible Mammalian Expression Systems

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Inducible Mammalian Expression Systems

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Inducible Mammalian Expression Systems

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Expression using Sindbis Virus

• Broad host range• High level expression

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Expression using Sindbis Virus

• Broad host range• High level expression

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Expression using Sindbis Virus

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Mammalian cell expression system

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 Gene expression in mammalian cell lines

A convenient alternative for setting up mammalian cell facilities – get a comprehensive service from us. We will achieve stable expression of the gene of your interest in mammalian cells.

Customer provides:

- Mammalian vector with the gene (cDNA) to be expressed. We accept plasmid and retroviral vectors - Sequence of the gene and map of the construct for transfection - Cell line or information about the cell line to be transfected.

Our service includes:

- Transfection of the cells. In case of a retroviral vector, virus production and cell infection - Antibiotic selection and generation of stable transfected (infected) cell clones. At least 10 independent clones will be selected and grown - Quantitative assay of the gene (cDNA) expression level in each transfected clone by RNA isolation followed by Northern hybridisation and/or RT-PCR - Selection of the best expressing clone - Cell freezing and depositing - Duration: 3-6 months (depending on the cell growth rate), allow 1month in addition if the cell line is not available in our collections

Customer receives:

- Detailed report on experiments and data obtained. - Two vials of transfected cells (the best expressing clone) - We will deposit the transfected cells in our collection as a precaution against accidental loss of the clone.

Price guide:

Price per transfection and selection of at least 10 clones: £3500.