S. Hendy et al., Rapid production of single-chain Fv fragments in plants using a potato virus X episomal vector, J IMMUNOL M, 231(1-2), 1999, pp. 137-146
We have used a plant virus episomal vector, based on potato virus X (PVX) t
o transiently express a single-chain Fv (scFv) and its diabody derivative i
n plants. The scFv was directed against a continuous epitope (cryptotope) o
n the coat protein of potato virus V. A cloned, full-length PVX vector sequ
ence, containing the scFv gene, was used to direct in vitro transcription a
nd the resulting RNA was used to inoculate Nicotiana clevelandii plants. Wi
thin a few days, plants developed characteristic symptoms and immunoblot an
alysis showed that accumulation of scFv protein coincided with accumulation
of PVX. Targeting of the scFv to the apoplast greatly increased protein ac
cumulation compared with cytosolic scFv and produced more severe symptoms o
n infected plants. ELISA demonstrated that the scFv and diabody extracted f
rom infected plants showed the same antigen-binding specificity as that of
the parental monoclonal antibody. The PVX vector is a convenient, rapid, lo
w-cost in planta expression system that can also be used. for assessment of
scFv production and function prior to stable plant transformation. (C) 199
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