Figure Legend :
A) Specific inhibitory activity of rhC1 inhibitor produced in CAP Go.2 was compared with a commercially available preparation of serum C1 Inh (Berinert).
B) Residual C1 Inh was measured in the serum of rats injected with conventional recombinant hC1 Inh, rhC1 Inh produced in CAP Go.2 cells or Berinert.
C) Serum half life of conventional recombinant hC1 Inh and C1 Inh produced in different CAP-Go cell lines in comparison to Berinert.
Human blood plasma as source for biotherapeutics is very limited and safety concerns still persist, leading to a growing need for recombinant plasma proteins. In addition, glycosylation patterns of most plasma proteins are very complex and represent a huge challenge to recombinant protein expression. With a comprehensive portfolio of glyco-optimized human cell lines, the CAP-Go expression system paves the way for recombinant plasma proteins.
Recombinant human C1 Inhibitor (C1-INH)
C1-Inhibitor deficiency patients suffer from an inherited form of angioedema that are currently predominantly being treated with intravenous injections of C1 Inhibitor purified from human serum. CEVEC´s CAP-Go derived C1 Inhibitor showed in a pivotal pharmacokinetic rat study a serum half life matching one of the two currently available, plasma derived treatments, Berinert®. This result, in combination with excellent specific activities of CAP-Go derived C1 Inh and commercially attractive production yields, paves now the way to develop a safer and more economic therapy for acute and prophylactic HAE indications. CEVEC plans to partner the further preclinical & clinical development of the molecule. For further information contact email@example.com or give us a call under +49 221 46020800.
Expression of recombinant human rhPLAP in CAP Go.1 or CAP Go.3 cells results in glyoproteins with increased sialylation of N-glycans and significantly increased serum half-life.
A) IEF gel analysis indicates a similar degree of sialylation of rhPLAP from CAP Go.1 and CAP Go.3. Conventional rhPLAP is significantly less sialylated.
B) rhPLAP pharmacokinetic studies comparing rhPLAP from CAP Go.1 or CAP Go.3 cells to conventional rhPALP in a rat animal study reveal an outstanding serum half-life of the material produced in CAP Go.1 and CAP Go.3 cells.
Placental alkaline Phophatase
Today, various alkaline Phosphatase (AP) isoforms are under development for the treatment of acute and chronic inflammatory diseases such as rheumatoid arthritis. Additionally, chronic degenerative diseases such as Alzheimer’s disease or Amyotrophic lateral sclerosis (ALS or Lou Gehrig’s disease) are being considered promising therapeutic indications for alkaline Phosphatases. Currently, ongoing clinical trials are being conducted with purified proteins from either bovine intestinal tissues or with non-naturally occurring reassembled recombinant versions of these molecules. The molecule developed by CEVEC, a recombinant placental human AP (rhPLAP) with a high, specific activity and a prolonged serum-half life, is expected to become the preferred alternative for these approaches. CEVEC plans to partner the further preclinical & clinical development of the molecule. For further information contact firstname.lastname@example.org or give us a call under +49 221 46020800.
Figure Legend left: rhHGF
High protein titer of recombinant human Hepatocyte Growth Factor, a plasma protein with 1 O-linked and 3 N-linked glycans, expressed in CAP Go cells. By single cell cloning yields could be improved 5-fold.
Figure Legend right: rhEPO
rhEPO transient or stable expressed in CAP Go cells display similar pattern of N-glycosylation as rhEPO stably expressed in CHO cells (SDS-PAGE after PNGaseF digestion).
Cytokines are small signaling molecules often involved in immunomodulation, oxidant stress or cell maturation processes like erythropoiesis. Comprising proteins, peptides and glycoproteins, they represent a heterogenous class of regulators.
Transient Expression of KV1.5 reporter gene in CAP T and HEK293 cells. The expression of the ion channel was detected in HEK293 by immunofluorescence labelling (a+b) using a monoclonal antibody (green). Transfected CAP-T (C) and HEK293 cells (D) were also analyzed for KV1.5 currents by automated patch-clamp using a Port-á-Patch (Nanion) and compared to mock transfected cells (A+B). Data by courtesy of Evotec (CCS Cell Culture service GmbH), Hamburg, Germany.
Ion channels are pore-forming and ion permeable membrane proteins which are able to produce and maintain a resting membrane potential as well as control ion flux and regulatory signaling.
Mammalian cells expressing functional ion channels are a valuable cell-based assay tool for drug screening.
CAP-Go cells are easy to handle, single cell suspension cultures which show outstanding sealing properties in automated patch clamp assays.
Expression in CAP Go cells results in
- gp120 titer > 30 mg/L = 5.6 pcd
- No degradation or aggregation in the CAP derived material
- CAP expressed gp120 appears to be more homogenously glycosylated than CHO derived material
- The project was conducted in cooperation with TCF GmbH and the University Medical Center of the Johannes Gutenberg-University Mainz, Department of Dermatology
VIRUS ENVELOPE PROTEINS
Virus envelope proteins are difficult to express highly glycosylated proteins, e.g. the HIV-1 envelope protein gp120 has 25 N-linked glycosylation sites.
HIGH MOLECULAR MASS MULTIMER PROTEIN COMPLEXES
Expression of high molecular multimeric protein complexes e.g. Fibrinogen (340 kD trimeric protein 2x(a+b+g)) in CAP Go cells results in high expression titers with significantly less degradation than in HEK293 cell derived Fibrinogen.
Originally developed for complex and hard-to-express proteins of human origin, the CAP-Go platform proved, also, to be excellent for the production of recombinant antibodies.
Next to high yields with consistent product quality, antibodies produced in CAP-Go offer the advantage of significantly higher levels of galactosylation than, for instance, those produced in CHO cells. Increased galactosylation can positively affect CDC activity of IgGs.