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Production of antibodies against microcystin-RR for the assessment of purified microcystins and cyanobacterial environmental samples

  • Fiona M. Young*
  • , James S. Metcalf
  • , Jussi A.O. Meriluoto
  • , Lisa Spoof
  • , Louise F. Morrison
  • , Geoffrey A. Codd
  • *Tämän työn vastaava kirjoittaja

Tutkimustuotos: LehtiartikkeliArtikkeliTieteellinenvertaisarvioitu

36 Sitaatiot (Scopus)

Abstrakti

Microcystins (MC) are cyanobacterial hepatotoxins responsible for animal-poisoning and human health incidents. Immunoassays provide a sensitive means to detect these toxins, although cross-reactivity characteristics of different antibodies are variable, and most antibodies have been produced against MC-LR. Here, we have produced the first polyclonal antibodies against the commonly occurring variant, MC-RR, and compared them with MC-LR antibodies for the analysis of purified MCs and cyanobacterial environmental samples. Both antisera cross-reacted with all MCs tested, and with the related cyanobacterial hepatotoxin nodularin-R, but not with non-toxic cyanobacterial peptides. In general, better cross-reactivity characteristics were observed with the MC-RR antisera and limits of quantification were lower for most variants, with all MCs tested and nodularin-R having limits of quantification of 0.31 nM or below. The antisera had different affinities to mixtures containing pooled MC-LR and MC-RR, with MC-LR antisera underestimating total MC concentration when MC-RR represented over 70% of the total MC pool. Both antisera correlated well with HPLC-UV data when incorporated into ELISAs to screen previously characterised environmental samples from Åland, Finland. MC-RR antisera are useful for screening samples containing multiple MCs, and particularly for samples primarily containing MC-RR variants.

AlkuperäiskieliEnglanti
Sivut295-306
Sivumäärä12
JulkaisuToxicon
Vuosikerta48
Numero3
DOI - pysyväislinkit
TilaJulkaistu - 1 syysk. 2006
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

Rahoitus

We thank the European Commission (EC TOXIC project, EVK1-CT2002-00107 and PEPCY project, QLRT-2001-02634) for support. FMY thanks the UK Natural Environment Research Council for a postgraduate research studentship.

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