Team:Potsdam Bioware/Project/Part Virus

Selection Module

Abstract Selection Module

The "selection module" comprises a set of methods to select the desired cell clones from the collection of cells each expressing one variant of the antibody construct. Depending on the needs, different selection methods might have specific advantages. We set up three methods, whereby two are well established but discontinuous: i) fluorescent activated cell sorting (FACS), which yields many data but requires expensive instrumentation and ii) magnetic beads, which are less expensive and easy to automatize; and last but not least, we develop iii) a novel continuously acting viral selection method. The latter method is based on the assumption that antibody presentation and affinity can be used to modulate viral infection. Virus particles displaying the desired antigen can then either deliver a growth promoting or inhibiting signal. We achieve this by manipulating virus-like particles based on the recombinant Adeno-Associated Virus (rAAV) to present the antigen on the viral surface by either genetic fusion to the capsid protein or by a general enzymatic coupling step using sortase ligation technology. So far we have tested cell sorting (FACS) based on antibody expression, we have coupled YFP, which is the antigen for our test antibody system, to magentic beads, and we have produced rAAV fused at the genetic level to the antigens YFP, CFP and the sortase ligation motif. As a growth inhibiting signal our virus particles deliver a thymidine kinase gene, which enables killing by ganciclovir, and as growth promoting signal a neomycin/geneticin resistance cassette. We are in the process to determine which selection method works the best.

Figure 1: schematic representation of the Selection Module: A virus infects cells with high affine antibodies. These cells survive.

Introduction

The selection module kicks in when the diverse set of antibodies is expressed on the surface of the cells. In our system each CHO cell couples the genotype of an antibody construct to the phenotype presented on the surface. Therefore, we can use all tools already available for selection of cell surface display systems. Reading literature on these methods we opted for fluorescent activated cell sorting (FACS) and magnetic beads.

The CHO cells express antibodies presenting them on the surface. To check if the antibodies are presented on the surface of the CHO cells we focused on different selection systems. Therefore, we used several methods like magnetic beads, preparative FACS and retargeted Adeno-associated virus (AAV). We separated the viral selection system in two parts according to the presented antibodies on the surface of the CHO cells. We designed the recombinant AAV2 to present the required antigens on the surface. One of the selection systems is based on the GFP-nanobody - YFP-antigen – complex and the other selection system is based on the anti-EGFR-antibody - EGFR complex. After a stable antigen-antibody-complex was formed, the virus infects the cells with a necessary gene for detection and selection.

AAV2 Selection system

Selection system of cells with Advanced Antibody Construct

The first selection system is based on the expression of several fluorescence proteins. The CHO cells present on their surface the GFP-nanobody. This nanobody binds GFP and YFP with a high affinity and high specificity. The recombinant AAV carries YFP on the surface to target specifically the CHO cells with GFP-nanobody and to infect them (figure 2).

Figure 2: schematic representation of the recombinant adeno-associated virus with YFP on the surface and CFP as gene of interest, binds to the antibody representing CHO cell

To examine the effect of the enzyme AID stably transfected in the CHO cells to induce the hypersomatic mutation, we designed a recombinant virus with CFP on the surface. GFP-nanobody expressed on CHO cells binds YFP, but not the closely related CFP. Our goal was to show the AID mutates the GFP-nanobody to an antibody with a higher affinity to CFP. Formation of a stable antigen-antibody complex enables the virus binding to the cell and infect it with a mVenus-signal. By excitation the infected cells could be visualized by shining with yellow colour (figure3).

Figure 3: schematic representation of the recombinant adeno-associated virus with CFP on the surface and YFP as Gene of interest, binds to the mutate antibody representing CHO cell

To select the cells with the desired antigens the Virus gives the cells a survival signal by infecting them. Virus with the same CFP-antigen on the surface couldn't bind to the GFP-nanobody. Altered by the AID GFP-nanobody binds CFP linked to the virus following by the infection with kanamycin resistance gene cassette. The kanamycin/neomycin gene codes for the aminoglycoside phosphotransferase enzyme, which inactivates by phosphorylation the aminoglycoside antibiotics such as geneticin (G418). Cultured in the correct Geneticin concentration, which was determined by titration against non-transfected controls, selection for stable transfectants is possible (figure 4).

Figure 4: schematic representation of the selection system using the neomycin as gene of interest and CFP on the surface binds to the mutate antibody representing CHO cell.

Selection system of cells with Smaller Antibody Construct

The second selection system consists of the EGFR-antigen binding to the anti-EGFR-antibody (scFv425). The scFv425 has a high affinity for EGFR-antigen. After a stable binding the cell would be transduced with transgene encoding for cyan fluorescence protein CFP. The fluorescence could detected at the CFP channel by an excitation at 405 nm and an emission at 425–475 nm. A higher transduction rate would mean the modification of anti-EGFR-antibody to a higher affinity to EGFR which was driven by Activation-induced cytidine deaminase (AID). The selection of cells with improved antibody also relies on the transduction of cells with kanamycin resistance gene cassette.

AAV2 Genome

AAV is a DNA virus with single stranded linear genome of 4.7 kb. The genome consists of two open reading frames rep and cap which are flanked by two inverted terminal repeats (ITR).

The rep gene located on the 5'-end of the genome encodes four overlapping multifunctional regulatory proteins. The transcription of the Rep proteins begins at the promoters p5 (Rep 78/Rep 68) and p19 (Rep 52/Rep 40). The two larger Rep proteins Rep78 and Rep68 are required for genome replication, the regulation of gene expression, and for site specific integration. The smaller Rep proteins Rep52 and Rep40 are involved in the encapsidation of the AAV-Genome.

The open reading frame cap on the 3'end of the AAV-genome encodes the three viral capsid proteins VP1, VP2, and VP3. The transcription of the mRNA is regulated by the p40 promoter. Alternative splicing results in two mRNA molecules: one encoding VP1 and the other VP2/ VP3. Application of an alternative splice acceptor removes the first AUG start codon for VP1. Thereby mRNA that is mainly formed encodes for the VP2 and VP3 capsid proteins. The first AUG codon in the transcript is the initiation codon for VP3. The translation of VP2 begins at an upstream ACG non-methionine start codon resulting in an approximately 10-fold lower translation of VP2. The stop codon of the three capsid proteins is identical. The stoichiometric ratio of the three capsid proteins VP1, VP2 and VP3 forming the icosahedral form is 1:1:10.

AAV2 Infection

AAV2 viruses kill cancer cells without harming healthy ones. Viruses cross the membrane by a process called penetration.

The virus particles present in the cell media come closer to the cells by diffusion. After several attachments to the cell membrane the virus binds to the cell receptors and enter the cell by receptor mediated endocytosis. There are three cell receptors playing a major role in non-effectivity. Ubiquitously expressed cell surface Heparan sulfate proteoglycan (HSPG) functions as a primary receptor account for the broad host range of AAV. aVß5 integrin and fibroblast growth factor 1 (FGFR-1) have a co-receptor activity for successful viral entry into the host cell. Bound AAV particles enter the cell very rapidly through clathrin mediated endocytosis. Each endosome carries a single AAV particle. After internalization the virus requires acidic environment for sufficient release into the cytosol. AAV accumulates in the perinuclear space and enters through the nuclear pore complex (NPC) into the nucleus, where uncoating and gene expression take place.

AAV2 Lytic and lysogenic pathways

After entry to the nucleus, AAV follows either lytic or lysogenic life cycle. In the presence of a helper virus, Adenovirus or Herpesvirus, the AAV is directed in a lytic life cycle. AAV undergoes a productive infection, which includes rapid replication in the nucleus and the later release of the new particles into the environment by bursting cells.

If there is no helper virus, AAV establish latency by integration into the host genome. The Rep expression is limited. When AAV infects a human cell, it integrates in a site-specific manner into the chromosome 19, called AAVS1. Essential components are the ITRs and the AAVS1 in cis and Rep proteins 78/68 in trans. Rep78/68 binds to the Rep-binding site (RBS) on ITR and unwinds the ITR at the terminal resolution site (trs).

The productive cycle is initiated by infecting with the helper virus, what affects stronger Rep expression and episomal AAV DNA replication. Rep proteins excise the AAV genes out of the host cell’s chromosome. The excised genes are replicated in the nucleus and the capsid proteins package the replicated genes in the cell. When a large number of these particles have assembled, the helper virus induces cell lysis and release the newly assembled particles into the environment.

Recombinant AAV2

AAV are replication-deficient parvoviruses. Although AAV can replicate in the absence of a helper virus, they require a co-infection of adenovirus for an efficient replication. To bypass the co-infection with adenoviruses, which is associated with disadvantages like the contamination of AAV preparation, all of the required genes of adenovirus were encoded on a helperplasmid. The helperplasmid consisting of adenovirus E2A, VA und E4 genes, is transfected in the AAV-293-cells, which stably express the adenovirus E1 gene. The production of infectious adeno-associated virus particles is able by co-transfecting the AAV-293 cells with four plasmids: the plasmid that carries the helper genes taken from adenovirus, a plasmid coding the protein fused on VP1 or VP2 cap-gene, a vector plasmid that contains the wildtype AAV2 Rep-Cap genes with VP2 or VP1 knock out and an AAV2 ITR-providing plasmid carrying the gene of interest (figure 5). The transgene cassette flanked by the ITRs is wrapped as a single strand in the virus capsid. The replication of the plasmid with transgene cassette is implemented with rep-proteins and enveloped in the viral capsid formed by cap-proteins.

Figure 5: schematic representation of the pHelper system for virus production in AAV-293 host cells

Magnetic beads selection system

Our advanced construct presents an anti-GFP activity. Therefore, we could design a selection system that uses magnetic beads coupled to Green Fluorescence Protein (GFP) as an alternative method to select cells presenting antibody on their surface. The system is based on the creation of sequence of proteins connected to the magnetic beads.
The magnetic beads that we used are the commercial product of Invitrogen® and they are originally coupled to streptavidin - Dynabeads®. Biotin binds to streptavidin with very high affinity and specificity. GFP is covalently coupled to the biotin. Because our antibody construct shows anti-GFP activity, it binds to GFP and can be pulled together with biotinylated GFP connected to magnetic beads with streptavidin (figure 6).

Figure 6:Dynabeads connected to the biotinylated GFP coupled to the CHO cell presenting antibody on the surface

FACS selection system

Fluorescent activated cell sorting enables the the characterization of each cell based on forward scatter, side scatter (i.e. size and granularity) and fluorescence in a variety of channels depending on the instrument. As at our institute the only cell sorter had only a 488 and 635 nm laser excitation, which was not suited to sort our GFP, YFP and mCHerry reporters, we turned to the cell sorting facility of the Deutsches Rheuma-Forschungszentrum Berlin (DRFZ). At this facility we tested sorting of the small antibody construct (YFP) in combination with AID expression (GFP) and the advanced antibody construct in combination (mCherry) with AID (GFP) based on the fluorescence of the reporter genes. For both constructs 300'000 double positive cells were sorted. Since the sorting was successful, we are confident that we can also sort cells based on the mCherry reporter and a fluorescently labeled antigen.

Results

Targeting the virus against the small antibody construct

To target the virus against the small construct of the antibody we designed plasmids required for viral assembly. EGF-receptor (EGFR) is a big protein which would disturb the viral assembly, so we focused on the enzyme sortase which covalently attaches proteins to each other. Expressed the third EGFR domain should contain the C-terminal Sortase motif to be recognized by the enzyme Sortase. N-terminal Sortase motif was fused to the N-terminus of VP2/3 gene of adeno-associated virus in the BioBricks (BBa_K929200 and BBa_K929201) to allow the ligation of third EGFR domain on the surface of virus by the Sortase.

The first plasmid with the N-terminal sortase motif was designed. The BioBrick pCMV_DARPin-E01_Middle-Linker_[AAV2]-VP23 was used to get the fusion parts linked to the VP2/3 cap-gene. The fusion parts Kozak sequence and the N-terminal sortase motif were constructed as a forward primer close to the VP2/3 – gene, which was used as an annealing part. The reversed primer was designed to enclose the whole VP2/3 region. For the following digestion the restriction sites for XbaI and PstI were also presented in the primers.

Amplificate product generated during the PCR was digested with the enzymes XbaI and PstI. Then it was ligated into the BioBrick containing the CMV promoter (figure 7)[http://partsregistry.org/Part:BBa_I712004 (BBa_I712004)].

Figure 7: sortase motiv cloned into PSB1C backbone (BBa_K929202)

The next extracellular ligand-binding domain of EGFR was constructed to be expressed in E. coli. The coding part for the ligand-binding domain was inserted downstream to the PelB sequence and upstream to the His-tag and C-terminal sortase motif. The constructed plasmid contain the RFC25 according suffix and prefix.

To express the EGFR ligand-binding domain in XL1-Blue E.coli strain the constructed part was ligated in the arabinose inducible promoter containing plasmid (pBAD). The expression was induced with arabinose and the incubation conditions were 4 h at 30 °C (figure 8).

Figure 8: expression of the 3rd EGFR domain in E. Coli detection was performed using SDS-PAGE and Western-blot

The EGFR constructed part was also cloned into the BioBrick containing the CMV promoter. [http://partsregistry.org/Part:BBa_I712004 (Bba_I712004)]. The resulting Biobrick (BBa_K929202) corresponds to the original RFC10 prefix and suffix. But the desired fusion parts PelB, EGF-Receptor_3rd domain, His-tag and C-terminal sortase motif have 2 additional enclosing restriction sites compatible with the RFC25. That means, that the Part 'PelB, EGF-Receptor_3rd domain, His-tag and C-terminal sortase motif' could be cut out with the enzymes XbaI and AgeI (figure 9).

Figure 9: sortase motiv and His-tag cloned into PSB1C backbone (Bba_K929200)

Targeting the virus against the advanced antibody construct

To modify the surface exposed proteins of the recombinant virus the desired genes were fused to the N-terminus of VP2 cap-gene. VP2 cap-gene is not essential for viral effectivity, what makes it an ideal candidate for the insertions of sequences to retarget the particle. Therefore, to reduce and to define the AAV tropism, the primary receptor motif, heparan sulphate proteoglycan motif, was knocked-out. The plasmids YFP fused to VP1, CFP fused to VP2, mVenus and CFP as gene of interest and the plasmids with VP2 and VP1 knock out. To get the completely assembled recombinant adeno-associated virus with the YFP on the surface and CFP as gene of interest, we transfected the AAV-293 cells with four plasmids: the plasmid YFP fused to VP1, the rep-cap plasmid with VP1 knock-out, phelper plasmid and the CFP as gene of interest.

The yellow fluorescence was detectible(figure 10), pointing out that the virus was completely assembled. To check whether the viral assembly worked we infected the AAV-HT1080 cells with the recombinant virus (figure 11), like it was described in the AAV Helper-Free System Instruction Manual. The next day several HT1080 cells were gleaming cyan by the excitation.

Figure 11: positive control – infected HT1080 cells with the recombinant adeno-associated virus with YFP on the surface and CFP as the Gene of interest. Cyan fluorescence are the indicator for a successful infection

Figure 10: negative control - non transfeced CHO-cells with the recombinant adeno-associated virus rAAV) .The rAAV are not able to infect the CHO-cells (without nanobody). A) unbleached B) bleached

To measure the genomic virus titer the real-time PCR was used. We are using a standard curve to measure copies of the rAAV (YFP on the surface and GOI = CFP)(figure 12). There are 3.47 copies of the virus in each PCR (figure 13).

Figure 12:genomic virus titer - quantification curves of the qPCR

Figure 13: genomic virus titer – cp-values

We also created a virus with CFP on its surface and mVenus as the gene of interest. We used the plasmids that were the vector plasmid with CFP fused to VP2, the rep-cap plasmid with VP2 knock-out, phelper plasmid and mVenus as gene of interest. The further task will be to test this virus construct by infecting the HT1080 cells. We expect yellow fluorescence of the HT1080 cells.

Selection system with antibiotic resistance

We designed primer to get the neomycin/kanamycin cassette into the plasmid containing the left and right ITR. To select the cells with the improved affinity of the antibody to the antigen the virus provide the cell with a survival signal. In the near feature we want to infect the cells with the virus containing the neomycin/kanamycin resistance gene cassette. The infected cells should be cultivated on media containing Gentamycin.

Coupling of nanobody with Magnetic Beads

The switch from antibody presentation to antibody secretion is induced by the Cre Recombinase. The supernatant was collected and incubated with magnetic beads coupled to GFP via biotin-streptavidin. While performing a western blot we detected a band at 41kDa which correlates with the size of the nanobody-Fc construct, showing that the expected GFP-nanobody binding occurs.

Western Blot of purified Nanobody-Fc from supernatant of cells co-transfected with Cre recombinase and advanced construct. Purification was carried out with magnetic beads. Correct band can be seen at 41kDa

Discussion

Materials and Methods

quantitative real-time PCR

The quantitative real-time polymerase chain reaction (qPCR) is one of the leading methods of the biological research. The significant difference between PCR and qPCR is the detection via fluorescence. The change in the fluorescence intensity can be detected in each cycle. This fluorescence is proportional to the amount of the PCR product. This technique allows the user to follow the PCR reaction in real time. Because of the digital acquisition of the fluorescence, there are no more post-PCR steps (like gel electrophoresis) necessary. (Kubista, M et al. 2006)(Heid, Chr. et al. 1996). Using a standard curve of known sequence copies, the amount of DNA of the samples can be exactly detected. For this detection an intercalating fluorescent dye, like SYBR green, is used. SYBR green is an unspecific florescence dye, which binds within the minor groove of the double stranded DNA. By binding into the DNA, the fluorescent signal increases significantly and can be detected.
We used the qPCR to determine the genomic virus titer. Therefore, the cellular and plasmid DNA left in our virus stocks have to be digested. For that reason 5 µL of the supernatant from pelleted cell lysate was treated with 7.5 µL DNaseI and 5 µL MgCl2 (c= 50 mM) in a final volume of 50 µL. Additionally, the samples were incubated at 37 °C for 30 min with a subsequent inactivation at 65 °C for 10 min. PCR reactions were carried out with 5 µL of our digested samples. (Rohr et al. 2002, Rohr et al. 2005)

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