A Multifunctional Single-Attachment-Point Reagent for Controlled Protein Biotinylation
被引:7
作者:
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Garanger, Elisabeth
[1
,2
]
Weissleder, Ralph
论文数: 0引用数: 0
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机构:
Massachusetts Gen Hosp, Ctr Mol Imaging Res, Boston, MA 02129 USA
Harvard Univ, Sch Med, Boston, MA 02129 USA
Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
Harvard Univ, Sch Med, Boston, MA 02114 USAMassachusetts Gen Hosp, Ctr Mol Imaging Res, Boston, MA 02129 USA
Weissleder, Ralph
[1
,2
,3
,4
]
论文数: 引用数:
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Josephson, Lee
[1
,2
]
机构:
[1] Massachusetts Gen Hosp, Ctr Mol Imaging Res, Boston, MA 02129 USA
[2] Harvard Univ, Sch Med, Boston, MA 02129 USA
[3] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
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.