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Characterization of a CC49-Based Single-Chain Fragment−β-Lactamase Fusion Protein for Antibody-Directed Enzyme Prodrug Therapy (ADEPT)
- Source :
- Bioconjugate Chemistry. 17:410-418
- Publication Year :
- 2006
- Publisher :
- American Chemical Society (ACS), 2006.
-
Abstract
- CC49 is a clinically validated antibody with specificity for TAG-72, a carbohydrate epitope that is overexpressed and exposed on the cell surface in a large fraction of solid malignancies. We constructed a single-chain fragment (scFv) based on CC49 and fused it to beta-lactamase (BLA). Following optimization of the scFv domain by combinatorial consensus mutagenesis (CCM) for increased expression and stability, we characterized the protein variant for binding, in vivo pharmacokinetics (PK), and antitumor efficacy. The fusion protein TAB2.5 possessed a similar binding specificity relative to the parent antibody CC49. TAB2.5 also showed prolonged retention (T(1/2) = 36.9 h) in tumor-bearing mice with tumor/plasma ratios of up to 1000. Preliminary evaluation of TAB2.5, in combination with a novel prodrug, GC-Mel, resulted in significant efficacy in a colorectal xenograft tumor model and supports the utility of the protein as an agent for tumor-selective prodrug activation.
- Subjects :
- Antibodies, Neoplasm
Recombinant Fusion Proteins
Cell
Immunoglobulin Variable Region
Biomedical Engineering
Mice, Nude
Pharmaceutical Science
Mutagenesis (molecular biology technique)
Bioengineering
Irinotecan
beta-Lactamases
Epitope
Mice
Drug Delivery Systems
medicine
Animals
Humans
Prodrugs
Antineoplastic Agents, Alkylating
Immunoglobulin Fragments
Melphalan
Binding selectivity
Pharmacology
Drug Carriers
Antibiotics, Antineoplastic
Molecular Structure
biology
Chemistry
Organic Chemistry
Adept
Prodrug
Antineoplastic Agents, Phytogenic
Fusion protein
Molecular biology
Cephalosporins
medicine.anatomical_structure
Biochemistry
Doxorubicin
Nitrogen Mustard Compounds
biology.protein
Camptothecin
Female
Antibody
Colorectal Neoplasms
Neoplasm Transplantation
Biotechnology
Subjects
Details
- ISSN :
- 15204812 and 10431802
- Volume :
- 17
- Database :
- OpenAIRE
- Journal :
- Bioconjugate Chemistry
- Accession number :
- edsair.doi.dedup.....240871119dc39749e0e8b1fb0c6a9c29
- Full Text :
- https://doi.org/10.1021/bc0503521