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Binding competition of okadaic acid derivatives to anti-okadaic acid antibody.

作者信息

Yatsunami J, Fujiki H, Suganuma M, Nishiwaki S, Ojika M, Yamada K, Levine L

机构信息

Cancer Prevention Division, National Cancer Center Research Institute, Tokyo, Japan.

出版信息

Toxicon. 1991;29(11):1409-12. doi: 10.1016/0041-0101(91)90129-f.

Abstract

The serologic activities of structurally related okadaic acid derivatives have been determined. Binding of [3H]okadaic acid to rabbit anti-okadaic acid is inhibited with equal effectiveness by okadaic acid, dinophysistoxin-1, acanthifolicin, okadaic acid tetramethyl ether, and okadaic acid spiroketal II. Okadaic acid spiroketal I, which lacks the F- and G-rings of okadaic acid, inhibits serologic binding about 60 times less effectively. The F- and G-rings of okadaic acid may comprise part of the epitopes recognized by some of the polyclonal antibodies.

摘要

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