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Characterization of a CC49-Based Single-Chain Fragment−β-Lactamase Fusion Protein for Antibody-Directed Enzyme Prodrug Therapy (ADEPT)

Authors :
Joshua Roy Basler
Lilia Babé
Peter D. Senter
Volker Schellenberger
Enrique Escandon
Ralph F. Alderson
Martin Roberge
Wei Geng
Brian E. Toki
Regina Chin
Roanna Ueda
Judith A. Fox
Tianling Chen
Amy Liu
Tessi Kanavarioti
Douglas Hodges
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.

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