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Cloning and plant-based production of antibody MC10E7 for a lateral flow immunoassay to detect [4-arginine]microcystin in freshwater.
Melnik, Stanislav; Neumann, Anna-Cathrine; Karongo, Ryan; Dirndorfer, Sebastian; Stübler, Martin; Ibl, Verena; Niessner, Reinhard; Knopp, Dietmar; Stoger, Eva.
Afiliação
  • Melnik S; Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria.
  • Neumann AC; Institute of Hydrochemistry and Chair for Analytical Chemistry, Technical University Munich, Munich, Germany.
  • Karongo R; Institute of Hydrochemistry and Chair for Analytical Chemistry, Technical University Munich, Munich, Germany.
  • Dirndorfer S; Institute of Hydrochemistry and Chair for Analytical Chemistry, Technical University Munich, Munich, Germany.
  • Stübler M; Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria.
  • Ibl V; Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria.
  • Niessner R; Institute of Hydrochemistry and Chair for Analytical Chemistry, Technical University Munich, Munich, Germany.
  • Knopp D; Institute of Hydrochemistry and Chair for Analytical Chemistry, Technical University Munich, Munich, Germany.
  • Stoger E; Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria.
Plant Biotechnol J ; 16(1): 27-38, 2018 01.
Article em En | MEDLINE | ID: mdl-28421663
Antibody MC10E7 is one of a small number of monoclonal antibodies that bind specifically to [Arg4]-microcystins, and it can be used to survey natural water sources and food samples for algal toxin contamination. However, the development of sensitive immunoassays in different test formats, particularly user-friendly tests for on-site analysis, requires a sensitive but also cost-effective antibody. The original version of MC10E7 was derived from a murine hybridoma, but we determined the sequence of the variable regions using the peptide mass-assisted cloning strategy and expressed a scFv (single-chain variable fragment) format of this antibody in yeast and a chimeric full-size version in leaves of Nicotiana tabacum and Nicotiana benthamiana to facilitate inexpensive and scalable production. The specific antigen-binding activity of the purified antibody was verified by surface plasmon resonance spectroscopy and ELISA, confirming the same binding specificity as its hybridoma-derived counterpart. The plant-derived antibody was used to design a lateral flow immunoassay (dipstick) for the sensitive detection of [Arg4]-microcystins at concentrations of 100-300 ng/L in freshwater samples collected at different sites. Plant-based production will likely reduce the cost of the antibody, currently the most expensive component of the dipstick immunoassay, and will allow the development of further antibody-based analytical devices and water purification adsorbents for the efficient removal of toxic contaminants.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoensaio / Água / Microcistinas Idioma: En Revista: Plant Biotechnol J Assunto da revista: BIOTECNOLOGIA / BOTANICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoensaio / Água / Microcistinas Idioma: En Revista: Plant Biotechnol J Assunto da revista: BIOTECNOLOGIA / BOTANICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Áustria