Although much progress has been made in the production of recombinant
antibodies and their fusions, there are still problems with solubility
and folding. Useful antibodies produced from cloned hybridomas do not
always result in scFvs behaving favourably. We report here further wo
rk on an scFv (H17E2) against the oncofetal antigen human placental al
kaline phosphatase. The overall expression was greatly improved and th
e H17E2 scFv was redesigned by manipulation of the interdomain linker,
resulting in much higher expression levels of the soluble scFv in its
active conformation at 0.2-0.5 mg/l of bacterial culture. We show tha
t the new soluble version of this scFv has similar characteristics to
the refolded version in terms of antigen and tumour cell binding, stab
ility and in vivo pharmacokinetics. The final tumour uptake behaviour
of these scFvs is superior to that of the parental whole antibody with
respect to tumour:organ ratios, but still requires further developmen
t before considering it as a suitable molecule for clinical use in ova
rian or testicular cancer.