Controlled coupling of aminoglycoside antibiotics to proteins for use in homogeneous enzyme immunoassays

Selective N-acylation of aminoglycoside antibiotics with the N-hydroxysuccinimide ester of methyldithioacetic acid, followed by reaction with methanethiol or dithioerythritol, gives sulfhydryl labeled antibiotics. Alternatively, the nucleophilic sulfhydryl group is incorporated into an antibiotic by...

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Veröffentlicht in:Canadian journal of chemistry 1984-01, Vol.62 (11), p.2471-2477
Hauptverfasser: Singh, Prithipal, Pirio, Marcel, Leung, Danton K, Tsay, Yuh-Geng
Format: Artikel
Sprache:eng
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Zusammenfassung:Selective N-acylation of aminoglycoside antibiotics with the N-hydroxysuccinimide ester of methyldithioacetic acid, followed by reaction with methanethiol or dithioerythritol, gives sulfhydryl labeled antibiotics. Alternatively, the nucleophilic sulfhydryl group is incorporated into an antibiotic by treatment with N-acetyl-d,l-homocysteine thiolactone. These derivatives couple readily with proteins that have previously been modified with bromoacetylglycyl groups to provide conjugates for use in the development of homogeneous enzyme immunoassays.
ISSN:0008-4042
1480-3291
DOI:10.1139/v84-425