Rapid production of single-chain Fv fragments in plants using a potato virus X episomal vector

Simon Hendy, Zhao Chun Chen, Hugh Barker, Simon Santa Cruz, Scan Chapman, Lesley Torrance, William Cockburn, Garry C. Whitelam*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

40 Citations (Scopus)

Abstract

We have used a plant virus episomal vector, based on potato virus X (PVX) to transiently express a single-chain Fv (scFv) and its diabody derivative in plants. The scFv was directed against a continuous epitope (cryptotope) on the coat protein of potato virus V. A cloned, full-length PVX vector sequence, containing the scFv gene, was used to direct in vitro transcription and the resulting RNA was used to inoculate Nicotiana clevelandii plants. Within a few days, plants developed characteristic symptoms and immunoblot analysis showed that accumulation of scFv protein coincided with accumulation of PVX. Targeting of the scFv to the apoplast greatly increased protein accumulation compared with cytosolic scFv and produced more severe symptoms on infected plants. ELISA demonstrated that the scFv and diabody extracted from infected plants showed the same antigen- binding specificity as that of the parental monoclonal antibody. The PVX vector is a convenient, rapid, low-cost in planta expression system that can also be used for assessment of scFv production and function prior to stable plant transformation. (C) 1999 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)137-146
Number of pages10
JournalJournal of Immunological Methods
Volume231
Issue number1-2
DOIs
Publication statusPublished - 10 Dec 1999

Keywords

  • Plant virus vector
  • Potato virus X
  • Single-chain Fv

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