Hepatitis C Virus Vaccine Development Service
Glycoproteins in Hepatitis C Virus (HCV)
There are two glycoproteins: E1 and E2 in HCV. Both proteins are immunogenic and induce the generation of neutralizing antibodies. At the same time, they are involved in the viral invasion of cells. There is no vaccine for HCV. The difficulty in developing one is the difficulty in obtaining suitable immunogens that can elicit a good adaptive immune response from the body. Antibodies against viral cytosolic glycoproteins play a crucial role in the rapid clearance of HCV viremia. The envelope glycoprotein of HCV is therefore an ideal target for immunogen design. It is found that a vaccine expressing recombinant E1 and E2 proteins co-immunized with Adjuvant successfully induced the generation of neutralizing antibodies and multifunctional CD4+ T cell responses.
Fig.1 Structure of HCV. (Wikipedia)
HCV Vaccine Development Service at CD BioGlyco
CD BioGlyco aims to promote HCV Vaccine Development. The main types of vaccines currently available are DNA vaccines, vector vaccines, and protein vaccines. The envelope proteins E1 and E2 are potential immunogens for vaccine development. We provide glycoprotein vaccine development services based on the two proteins.
We focus on two proteins and analyze their immunogenicity and other characteristics. We also initially evaluate the effectiveness of two proteins as vaccine candidates. We will construct recombinant plasmids and transfer them into expression systems such as Yeast, etc. Protein purification is also one of the difficulties in vaccine development. We optimize the conditions for efficient and stable protein expression, which greatly improves the purification efficiency.
Most HCV protein subunit vaccines are mainly for the production of secreted E2. However, it only induces low levels of neutralizing antibody production. Recombinant Glycoprotein Vaccines are mainly designed to induce neutralizing antibody responses for the prevention and control of HCV infection. We construct different forms of recombinant E1 and E2 proteins and screen their optimal forms. Multi-epitope vaccines carry multiple antigenic epitopes of the virus due to their simultaneous carriage. In addition to the absence of virulence rebound, it can also be induced to elicit an immune response from the body. We also offer HCV multi-epitope vaccine development services.
Fig.2 Process of HCV vaccine development. (CD BioGlyco)
Applications
- Neutralizing antibodies against viral cytosolic glycoproteins E1 and E2 play an important role in the rapid clearance of HCV viremia. Our HCV vaccine development services include the production of recombinant E1 and E2, which can be used for antibody development.
- Early diagnosis of HCV infection is important in controlling HCV transmission. Our HCV vaccine development services include the production of E1 and E2, which can be utilized for HCV assay research.
Highlights
- The yeast expression system we use can effectively overcome the lack of protein post-translational processing and modification in the Escherichia coli system. Expression of exogenous proteins can be secreted extracellularly, which facilitates the isolation and purification of products.
- E1 and E2 protein purification cause the slow development of the HCV vaccine. We optimize the protein purification method and greatly improve the protein recovery rate.
- We have rich experience in immunoassay and provide perfect quantitative detection of cytokines, cellular immunoassay, and other vaccine evaluation services.
CD BioGlyco provides vaccine development clients with a one-stop shop for vaccine design and production. In addition to HCV vaccines, we also provide the SARS Corona Virus and West Nile Virus Vaccine Development Services. If you have any questions or needs about vaccine development, please feel free to contact us for consultation. We will contact you as soon as possible.
References
- From Wikipedia: https://upload.wikimedia.org/wikipedia/commons/7/78/Hegasy_Hep_C_Virus_EN-01.jpg
- Beaumont, E.; et al. Chimeric hepatitis B virus/hepatitis C virus envelope proteins elicit broadly neutralizing antibodies and constitute a potential bivalent prophylactic vaccine. Hepatology. 2013, 57(4): 1303-1313.
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Resources
- Glyco™ Synthesis Platform
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- Site Occupation
- Glycoprotein Structure Analysis
- Glycosylation Site-specific Antibody-Drug Conjugate (ADC) Development Platform
- Carbohydrate-based Glycomedicine Development Platform
- By Sources of Carbohydrate
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- By Applications of-based Glycomedicines
- Carbohydrate-based Anticoagulant Glycomedicine Development
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- Carbohydrate-based Antidiabetic Glycomedicine Development
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- Carbohydrate-based Antiviral Glycomedicines Development
- Carbohydrate-based Antiparasiti Glycomedicine Development
- By Discovery Strategies
- Glycoengineering-based Glycomedicine Development
- Production of Food Ingredients
- Multi-omics Platform for Cancer Glucose Metabolism (MOPCGM)
- Cancer Cell Glycolytic Analysis
- Cancer Cell TCA Cycle Analysis
- Cancer Cell PPP Analysis
- Gene-level Regulation Analysis of Cancer Glucose Metabolism
- Interplay Between Glucose Metabolism Reprogramming and Tumorigenesis & Progression
- Interplay Between Glucose Metabolism Reprogramming and Proliferative Signaling
- Interplay Between Glucose Metabolism Reprogramming and Growth Suppressor
- Interplay Between Glucose Metabolism Reprogramming and Cancer Cell Death
- Interplay Between Glucose Metabolism Reprogramming and Replicative Immortality
- Interplay Between Glucose Metabolism Reprogramming and Angiogenesis
- Interplay Between Glucose Metabolism Reprogramming and Invasion & Metastasis
- Interplay Between Glucose Metabolism Reprogramming and Immune Escape
- Interplay Between Glucose Metabolism Reprogramming and Genomic Instability
- Interplay Between Glucose Metabolism Reprogramming and Tumor-associated Inflammation
- Glucose Metabolism-Microenvironment Crosstalk Analysis in Cancer
- Cancer Glucose Metabolism In Vivo Analysis
- Applications of Studing Cancer Glucose Metabolism
- Discovery of Cancer Glucose Metabolism Small Molecule Inhibitor
- Discovery of Cancer Glucose Metabolism Therapeutic Monoclonal Antibodies
- Development of Gene Therapy Targeting Cancer Glucose Metabolism
- Discovery of Cancer Glucose Metabolism CAR-T Therapy Targeting
- Discovery of Cancer Glucose Metabolism Combination Therapy Strategy
- Discovery of Cancer Glucose Metabolism Precision Therapeutic Strategies
- Glycoengineering Platform
- Therapeutic Nucleic Acid Development Platform
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- Biological Evaluation Service for Therapeutic Oligonucleotide
- mRNA-based Vaccine Development Service
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- mRNA Structural Characterization
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- Glycobiology Microarray Platform
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- Carbohydrate-based Vaccine Development
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- Tumor-Associated Carbohydrate Vaccine Development
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- Carrier Protein Design Service
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- Carbohydrate-based Adjuvant Development
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- Glycoprotein-based Vaccine Development
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- Glycogenomics Platform
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- Cancer Glycogene Discovery Service
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- Glycan Display Platform
- Traditional Glycan Display Array
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- Cell-based Glycan Display Array
- Neoglycolipid (NGL) Display Array
- Liquid Glycan Display Array (LiGA)
- Glycophage Display
- N-linked Glycoprotein-based Glycophage Display System Construction Service
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- Glycophage Display-based Glycosylase Genetic Analysis Service
- Glycophag Display-based Glycoarray Service
- Glycophage Display-based Antibody Development Service
- Glycophage Display-based Epitope Mapping Service
- Glycophage Display-based Biomarker Development Service
- De Novo Glycan Display
- Cell-Surface Glycan Editing
- Examining the Effects of Altering Blood Group Antigens on Erythrocyte Cell Surfaces
- Preventing Cellular Rejection During Transplantation
- Modulating Chemical Composition and Physical Parameters of Glycocalyx
- Tailoring Cell Membranes with Biologically Active Glycans
- Targeting Glycosaminoglycan-mediated Growth Factor Signaling to Influence Stem Cell Specification
- Long-term De Novo Glycan Display for Directing Stem Cell Fate
- Traditional Glycan Display Array
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- PEG Glyconanoparticle
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- Fluorescent Glyconanoparticle
- Silica Glyconanoparticle
- Liposome Glyconanoparticle
- Glycol Nanohydrogel Development
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- Glycol Nanocrystal/Nanosheet/Nanosphere/Nanofiber
- Glyconanoparticle Preclinical Study
- Glyconanoparticle Formulation
- Glyconanotechnology-based Biosensor Development
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