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• W2023628417 abstract "[ 15 N]‐heteronuclear single quantum coherence (HSQC) spectra provide a readily accessible fingerprint of [ 15 N]‐labelled proteins, where the backbone amide group of each nonproline amino acid residue contributes a single cross‐peak. Cell‐free protein synthesis offers a fast and economical route to enhance the information content of [ 15 N]‐HSQC spectra by amino acid type selective [ 15 N]‐labelling. The samples can be measured without chromatographic protein purification, dilution of isotopes by transaminase activities are suppressed, and a combinatorial isotope labelling scheme can be adopted that combines reduced spectral overlap with a minimum number of samples for the identification of all [ 15 N]‐HSQC cross‐peaks by amino acid residue type. These techniques are particularly powerful for tracking [ 15 N]‐HSQC cross‐peaks after titration with unlabelled ligand molecules or macromolecular binding partners. In particular, combinatorial isotope labelling can provide complete cross‐peak identification by amino acid type in 24 h, including protein production and NMR measurement." @default.
• W2023628417 created "2016-06-24" @default.
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• W2023628417 date "2006-08-23" @default.
• W2023628417 modified "2023-10-15" @default.
• W2023628417 title "15N-Labelled proteins by cell-free protein synthesis." @default.
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• W2023628417 doi "https://doi.org/10.1111/j.1742-4658.2006.05433.x" @default.
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