Lectin-dependent inhibition of antigen-antibody reaction: application for measuring α2,6-sialylated glycoforms of transferrin

We developed a high-throughput Enzyme-linked immunosorbent assay (ELISA) for measuring α2,6-sialylated transferrin (Tf), based on inhibition of anti-Tf antibody binding to α2,6-sialylated Tf by a lectin, Sambucus sieboldiana Agglutinin (SSA). The inhibition was not observed with other glycoforms, su...

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Veröffentlicht in:Journal of biochemistry (Tokyo) 2013-09, Vol.154 (3), p.229-232
Hauptverfasser: Hoshi, Kyoka, Kariya, Yoshinobu, Nara, Kiyomitsu, Ito, Hiromi, Matsumoto, Kana, Nagae, Masamichi, Yamaguchi, Yoshiki, Nakajima, Madoka, Miyajima, Masakazu, Arai, Hajime, Kuno, Atsushi, Narimatsu, Hisashi, Shirotani, Keiro, Hashimoto, Yasuhiro
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Sprache:eng
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Zusammenfassung:We developed a high-throughput Enzyme-linked immunosorbent assay (ELISA) for measuring α2,6-sialylated transferrin (Tf), based on inhibition of anti-Tf antibody binding to α2,6-sialylated Tf by a lectin, Sambucus sieboldiana Agglutinin (SSA). The inhibition was not observed with other glycoforms, such as periodate-treated, sialidase-treated and sialidase/galactosidase-treated Tf, suggesting that the assay was glycoform specific. This finding was applied to an automated latex-agglutination immunoassay, using SSA lectin as an inhibitor (SSA-ALI). The concentration of α2,6-sialylated Tf measured by SSA-ALI in human cerebrospinal fluid was correlated with that of ELISA (r2 = 0.8554), previously developed for measuring α2,6-sialylated Tf.
ISSN:1756-2651
DOI:10.1093/jb/mvt065