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A Multifunctional Single-Attachment-Point Reagent for Controlled Protein Biotinylation
Author(s) -
Élisabeth Garanger,
Ralph Weissleder,
Lee Josephson
Publication year - 2008
Publication title -
bioconjugate chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.279
H-Index - 172
eISSN - 1520-4812
pISSN - 1043-1802
DOI - 10.1021/bc800392t
Subject(s) - biotinylation , biotin , chemistry , avidin , reagent , streptavidin , fluorophore , combinatorial chemistry , bifunctional , substrate (aquarium) , fluorescence , biochemistry , organic chemistry , physics , oceanography , quantum mechanics , geology , catalysis
The biotin/avidin system is one of the most widely used affinity detection and affinity capture systems in biology. However, the determination of the exact number of biotin tags attached onto a substrate is complicated by the fact that biotin does not present any light-absorbing or -emitting properties. Here, we describe a fluorescent biotinylation reagent designed from the general multifunctional single-attachment-point (MSAP) reagent concept. A Lys-Cys dipeptide scaffold was used to display a biotin functional group and a fluorescein functional group along with an N-hydroxysuccinimide ester reactive group. The resulting bifunctional MSAP reagent, Fl-Biotin-NHS, was used to prepare a monobiotinylated version of cetuximab, which was further reacted with avidin to obtain a soluble avidin-based cetuximab oligomer. The MSAP peptide-scaffold approach allows fluorophores, chromophores, or reactive groups to be combined with biotin and provides a broad approach to obtain multifunctional biotin-based reagents.

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