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• W2795880452 abstract "The quadricyclane (QC) ligation is a bioorthogonal reaction between a quadricyclane moiety and a nickel bis(dithiolene) derivative. Here we show that a QC amino acid can be incorporated into a protein site-specifically using the pyrrolysine-based genetic code expansion platform, and subsequently used for ligation chemistry. Additionally, we exploited the photolability of the QC ligation product to render the adduct cleavable with a handheld UV lamp. We further developed a protein purification method that involves QC ligation of biotin to a protein of interest, capture on streptavidin resin, and finally release using only UV light. The QC ligation thus brings novel chemical manipulations to the realm of bioorthogonal chemistry." @default.
• W2795880452 created "2018-04-13" @default.
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• W2795880452 date "2018-10-01" @default.
• W2795880452 modified "2023-09-24" @default.
• W2795880452 title "Site-specific incorporation of quadricyclane into a protein and photocleavage of the quadricyclane ligation adduct" @default.
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• W2795880452 doi "https://doi.org/10.1016/j.bmc.2018.04.009" @default.
• W2795880452 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6170726" @default.
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