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• W3104893025 abstract "Protein-protein interactions (PPIs) play crucial roles in regulating essentially all cellular processes. Photo-cross-linking represents a powerful method to study PPIs. To fulfil the requirements for the exploration of different PPIs, there is a continuous demand on the development of novel photo-reactive amino acids with diverse structural properties and functionalities. Reported herein is the development of a bifunctional amino acid termed dzANA, which contains a diazirine, for photo-cross-linking, and a terminal alkyne group, for bioorthogonal tagging. Using known PPIs between histone posttranslational modifications (PTMs) and their binding partners as models, we demonstrate that the dzANA-harbouring peptide-based photoaffinity probes could efficiently and selectively capture the weak and transient PPIs mediated by histone modifications. Our study indicates the potential of dzANA to identify and characterize unknown PPIs." @default.
• W3104893025 created "2020-11-23" @default.
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• W3104893025 date "2020-01-01" @default.
• W3104893025 modified "2023-10-14" @default.
• W3104893025 title "A bifunctional amino acid to study protein–protein interactions" @default.
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• W3104893025 doi "https://doi.org/10.1039/d0ra09110c" @default.
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