Abstract

The rapid development of biomolecular NMR spectroscopy in the last decade(s) has paved the way for novel insights into the structure, dynamic properties, as well as the interaction of proteins. However, NMR data interpretation of large protein complexes is only feasible if the corresponding sample is selectively enriched in NMR active nuclei ( 13 C and 15 N) and/or 1 H-depleted by 2 H incorporation. One important strategy for selective protein isotope labeling is given by the addition of metabolic amino acid precursor compounds to the growth medium of a protein-overexpressing microorganism. Herein, we highlight the synthetic concepts to access these precursors from commercially available isotope sources. 1 Introduction 2 Aliphatic Residue Precursors 3 Aromatic Residue Precursors 4 Precursors of Other Labeled Residues 5 Conclusions

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