Selective Lsotopic labeling of recombinant proteins using amino acid auxotroph strains

James W. Whittaker

Research output: Chapter in Book/Report/Conference proceedingChapter

24 Scopus citations


Labeling proteins with stable isotopes is important for many analytical and structural techniques, including NMR spectroscopy and mass spectrometry. Nonselective labeling, which uniformly labels all amino acids in the protein, may be accomplished with readily available wild-type expression hosts. However, there are often advantages to labeling a specific amino acid, and residue-selective labeling generally requires the use of an expression strain that is auxotrophic for the amino acid in order to efficiently incorporate the isotopic label. The behavior of an auxotrophic strain may be complicated by the regulatory properties of the biosynthetic pathway, by secondary nutritional requirements resulting from disruption of a biosynthetic pathway, and from acquired sensitivity to environmental factors resulting from build-up of metabolic intermediates. As a result, it is important to characterize the phenotype of the each auxotrophic strain in order to optimize its performance as an expression host for selective labeling of proteins. The application of aromatic auxotroph strains of Pichia pastoris to labeling tyrosines in a recombinant protein (galactose oxidase) will be used to illustrate selective-labeling methods.

Original languageEnglish (US)
Title of host publicationPichia Protocols, Second Edition
EditorsJames M Cregg
Number of pages13
StatePublished - Aug 8 2007
Externally publishedYes

Publication series

NameMethods in Molecular Biology
ISSN (Print)1064-3745


  • Amino acid labeling
  • Auxotroph
  • EPR
  • Isotope
  • Isotopic labeling
  • Mass spectrometry
  • NMR
  • Phenylalanine
  • Spectroscopy
  • Tryptophan
  • Tyrosine

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics


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