SBIR-STTR Award

Trimer-Tag: A Technology For Producing Trivalent Biologics
Award last edited on: 1/31/12

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$224,700
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Peng Liang

Company Information

Genhunter Corporation

624 Grassmere Park Drive Suite 17
Nashville, TN 37211
   (615) 833-0665
   info@genhunter.com
   www.genhunter.com
Location: Single
Congr. District: 05
County: Davidson

Phase I

Contract Number: 1R43AI091286-01A1
Start Date: 7/15/11    Completed: 6/30/12
Phase I year
2011
Phase I Amount
$224,700
One of the modern strategies for treating autoimmune diseases such as rheumatoid arthritis and psoriasis involves the use of biologic TNF receptor decoys, such as soluble receptors or therapeutic antibodies, to intercept the inflammatory ligand TNF-1, and thus block the pathological activation of its receptors. However, current TNF-1 biologic blockers are all dimeric in structure, whereas TNF-1 itself is homotrimeric in nature. From a structural biology point of view, a homodimeric structure with a two-fold symmetry cannot perfectly dock to a homotrimeric structure with a three-fold symmetry, thus limiting the affinity between the two molecules. Here we describe a general methodology for efficient creation of trimeric soluble receptors as secreted proteins. The process involves gene fusion between a soluble receptor with a ligand binding domain or any biologically active protein and a trimerization tag from the C-propeptide domain of pro-collagen (Trimer-Tag), which is capable of self-assembly into a disulfide bond-linked trimer. We show that the homotrimeric soluble TNF receptor produced with such method is a more potent blocker than dimeric TNF receptor decoys in inhibiting TNF- 1 signaling in vitro. Moreover, we have also demonstrated that covalently strengthened homotrimeric TRAIL/Apo2L-Trimer ligand is a potent anticancer agent, in contrast to its dimeric Fc fusion counterpart. Thus, Trimer-Tag has the potential to become a new platform technology for rational design of the next generation biologic drugs against autoimmune diseases, cancer, AIDS, osteoporosis, and heart disease. In this Phase I SBIR application, we seek to significantly increase the expression level and optimize the purification scheme of these recombinant trimeric fusion proteins in the hope that this novel technology, which is covered by 3 U.S. patents, can quickly move from preclinical stage towards the bedsides of millions of patients.

Public Health Relevance:
This Phase I SBIR application seeks to further optimize and streamline a newly patented protein trimerization technology for the design and production of secreted therapeutic biologics targeting major diseases such as autoimmune diseases, cancer, AIDS, osteoporosis, and heart disease.

Thesaurus Terms:
Aids;Aids Virus;Apo2l;Acquired Immune Deficiency;Acquired Immune Deficiency Syndrome;Acquired Immune Deficiency Syndrome Virus;Acquired Immuno-Deficiency Syndrome;Acquired Immunodeficiency Syndrome;Acquired Immunodeficiency Syndrome Virus;Acquired Immunologic Deficiency Syndrome;Affinity;Aminoacetic Acid;Anti-Cancer Agents;Antineoplastic Agents;Antineoplastic Drugs;Antineoplastics;Apo-2l;Arthritis;Aspartate;Atrophic Arthritis;Autoimmune Diseases;Bmp-1;Bacteria;Bacteriophages;Binding Site Domain;Bioreactors;Blood Serum;Body Tissues;Cho Cells;Cachectin Receptors;Cancer Drug;Cancers;Carbamoyl Transferases;Cardiac Diseases;Cardiac Disorders;Cell Communication And Signaling;Cell Signaling;Cell Surface Antigens;Cell-Extracellular Matrix;Cells;Chimera Protein;Chimeric Proteins;Chinese Hamster Ovary Cell;Chromatography;Chromatography / Separation Science;Clinical;Clinical Treatment Moab;Codon;Codon Nucleotides;Collagen;Collagen Fibril;Complex;Dif;Disease;Disorder;Docking;Drug Design;Drugs;Ecm;Enbrel;Escherichia;Esteroproteases;Etanercept;Event;Extracellular Matrix;Family;Frequencies (Time Pattern);Frequency;Fusion Protein;Gene Amplification;Gene Fusion;Gene Transcription;Genetic Transcription;Glycine;Hiv;Hiv Envelope Glycoprotein Gp120;Hiv Envelope Protein Gp120;Hiv Env Protein Gp120;Htlv-Iii;Htlv-Iii Gp120;Heart Diseases;Homo;Human;Human Figure;Human Immunodeficiency Viruses;Human T-Cell Leukemia Virus Type Iii;Human T-Cell Lymphotropic Virus Type Iii;Human T-Lymphotropic Virus Type Iii;Human Body;Immunologic Surface Markers;Immunological Surface Markers;In Vitro;Infection;Inflammatory;Inflammatory Arthritis;Injection Of Therapeutic Agent;Injections;Intercept;Intracellular Communication And Signaling;L-Aspartate;Lav-Htlv-Iii;Legal Patent;Ligand Binding Domain;Ligands;Link;Logistics;Lymphadenopathy-Associated Virus;Malignant Neoplasms;Malignant Tumor;Mammalia;Mammals;Man (Taxonomy);Marketing;Mediating;Medication;Method Loinc Axis 6;Methodology;Methods;Modern Man;Molecular;Monoclonal Antibodies;N-Terminal;Nh2-Terminal;Nature;Neoplastic Disease Chemotherapeutic Agents;Non-Human Protein;Opgl;Osteoporosis;Patents;Patients;Peptidases;Peptide Hydrolases;Phages;Pharmaceutic Preparations;Pharmaceutical Preparations;Phase;Play;Process;Procollagen;Production;Proteases;Proteinases;Proteins;Proteolytic Enzymes;Psoriasis;Rankl;Rna Expression;Receptor Protein;Recombinants;Rheumatoid Arthritis;Sbir;Sbirs (R43/44);Scheme;Serum;Signal Transduction;Signal Transduction Systems;Signaling;Site;Small Business Innovation Research;Small Business Innovation Research Grant;Staging;Structure;Subcutaneous Injections;Surface Antigens;Suspension Culture;Tl2;Tnf;Tnf A;Tnf Receptor Family Protein;Tnf Receptor Superfamily;Tnf Receptors;Tnf Gene;Tnfr;Tnfsf10;Tnfsf10 Gene;Tnfsf11;Tnfsf11 Gene;Tnfsf2;Trail;Technology;Therapeutic;Therapeutic Antibodies;Tissues;Transcription;Translations;Tumor Necrosis Factor Gene;Tumor Necrosis Factor Receptor;Tumor Necrosis Factor Receptor Family;Tumor Necrosis Factor Receptor Superfamily;Tumor-Specific Treatment Agents;Type I Procollagen Carboxyl-Terminal Proteinase;Viral;Virus-Hiv;Yeasts;Analog;Anticancer Agent;Anticancer Drug;Arthritic;Autoimmune Disorder;Bacterial Virus;Base;Biological Signal Transduction;Bioprocess;Bone Morphogenetic Protein 1;Bone Morphogenic Protein 1;Carbamoyltransferase;Cost;Cytokine;Design;Designing;Disease/Disorder;Disulfide Bond;Drug/Agent;Expression Cloning;Fibrous Protein;Gene Product;Gene Synthesis;Gp120;Gp120 Env Glycoprotein;Gp120(Hiv);Hrankl2;Heart Disorder;Immunogenicity;Joint Inflammation;Malignancy;Member;Molecular Assembly;Molecular Assembly/Self Assembly;Molecular Self Assembly;Natural Gene Amplification;Neoplasm/Cancer;New Technology;Next Generation;Novel Technologies;Polypeptide;Pre-Clinical;Preclinical;Procollagen C-Endopeptidase;Procollagen C-Protease;Procollagen C-Proteinase;Procollagen Endopeptidase (Carboxy Terminal Splitting);Psoriasiform;Psoriatic;Psoriatiform;Receptor;Response;Sodf;Self Assembly;Structural Biology;Therapeutic Target;Transcarbamoylase;Triple Helix

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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