Source:http://linkedlifedata.com/resource/pubmed/id/17438823
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2007-4-18
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pubmed:abstractText |
The microcystin (MC) producing P. rubescens occurs in pre-alpine lakes and may impact fishery success, bathing, and raw water quality. P. rubescens extracts, characterized via LC-MS, contained the two MC-RR variants [Asp3]MC-RR and [Asp3,Dhb7]MC-RR. The protein-phosphatase-inhibition assay (cPPIA with phosphatases 1 and 2A) in its capability to quantify [Asp3]MC-RR, [Asp3,Dhb7]MC-RR, and MC-RR was compared to HPLC-DAD and anti-Adda-ELISA. The IC50 values (PP1 and PP2A) determined for MC-LR, MC-RR, and [Asp3]MC-RR were in the same range (1.9-3.8 and 0.45-0.75 nM). A 50-fold higher concentration of [Asp3,Dhb7]MC-RR (29.8 nM) was necessary to inhibit the PP2A by 50%. The PP1-IC50 of [Asp3,Dhb7]MC-RR was 22-fold higher (56.4 nM) than those of the other MCs, suggesting that specific structural characteristics are responsible for its weaker PPI capacity. Western blots demonstrated that [Asp3,Dhb7]MC-RR does not covalently bind to PP1. [Asp3,Dhb7]MC-RR has comparable in vivo LD50 values to MC-RR, despite a far lower PP-inhibiting capacity, suggesting that toxicodynamic and toxicokinetic characteristics of [Asp3,Dhb7]MC-RR are responsible for its high in vivo toxicity. The data demonstrate that cPPIA analysis of [Asp3,Dhb7]MC-RR-containing samples prevent reliable MC determination and lead to underestimation of potential toxicity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Microcystins,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/protein phosphatase inhibitor-1,
http://linkedlifedata.com/resource/pubmed/chemical/protein phosphatase inhibitor-2
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0013-936X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
41
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2609-16
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pubmed:meshHeading |
pubmed-meshheading:17438823-Blotting, Western,
pubmed-meshheading:17438823-Chromatography, High Pressure Liquid,
pubmed-meshheading:17438823-Cyanobacteria,
pubmed-meshheading:17438823-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:17438823-Eutrophication,
pubmed-meshheading:17438823-Fresh Water,
pubmed-meshheading:17438823-Germany,
pubmed-meshheading:17438823-Inhibitory Concentration 50,
pubmed-meshheading:17438823-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:17438823-Lethal Dose 50,
pubmed-meshheading:17438823-Mass Spectrometry,
pubmed-meshheading:17438823-Microcystins,
pubmed-meshheading:17438823-Proteins,
pubmed-meshheading:17438823-Risk Assessment,
pubmed-meshheading:17438823-Toxicity Tests
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pubmed:year |
2007
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pubmed:articleTitle |
Analytical and functional characterization of microcystins [Asp3]MC-RR and [Asp3,Dhb7]MC-RR: consequences for risk assessment?
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pubmed:affiliation |
Environmental Toxicology, University of Konstanz, Germany.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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