We have engineered the filamentous fungus Trichoderma reesei to assemb
le and secrete immunologically authentic engineered Fab antibody fragm
ents into the culture medium. A major improvement in yield was achieve
d by fusing the heavy Fd chain to the T. reesei cellulase, CBHI. The y
ields of secreted, immunologically active Fab and CBHI-Fab fusion were
1 mg/l and 150 mg/l, respectively. The Fab fragment can be released f
rom the fusion protein CBHI-Fab by an extracellular T reesei protease.
There was no detectable difference in affinity for the antigen betwee
n the engineered Fab and the idiotypic antibody.