Literature DB >> 18762866

A simple method for amino acid selective isotope labeling of recombinant proteins in E. coli.

Kit I Tong1, Masayuki Yamamoto, Toshiyuki Tanaka.   

Abstract

A simple and user-friendly method of labeling protein selectively with amino acids in vivo is introduced. This technique does not require the use of transaminase-deficient or auxotrophic strains. By manipulating the product feedback inhibitory loops of the E. coli amino acid metabolic pathways and, if necessary, by using enzyme inhibitors, proteins were labeled efficiently in vivo even with amino acid types that are central to the metabolic pathways, such as glutamine. The sequential backbone resonance assignment of the Neh2 domain of Nrf2 transcriptional factor, an intrinsically disordered protein with high spectral degeneracy, was achieved using this labeling method.

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Year:  2008        PMID: 18762866     DOI: 10.1007/s10858-008-9264-0

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  37 in total

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Journal:  J Biomol NMR       Date:  2004-09       Impact factor: 2.835

2.  The past, present and future of cell-free protein synthesis.

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5.  Expression and nitrogen-15 labeling of proteins for proton and nitrogen-15 nuclear magnetic resonance.

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Journal:  Proteins       Date:  2005-05-15

8.  NMR experiments for resonance assignments of 13C, 15N doubly-labeled flexible polypeptides: application to the human prion protein hPrP(23-230).

Authors:  A Liu; R Riek; G Wider; C von Schroetter; R Zahn; K Wüthrich
Journal:  J Biomol NMR       Date:  2000-02       Impact factor: 2.835

9.  Uniform and residue-specific 15N-labeling of proteins on a highly deuterated background.

Authors:  Jocelyne Fiaux; Eric B Bertelsen; Arthur L Horwich; Kurt Wüthrich
Journal:  J Biomol NMR       Date:  2004-07       Impact factor: 2.835

10.  EcoCyc: a comprehensive database resource for Escherichia coli.

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  29 in total

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2.  Probing ground and excited states of phospholamban in model and native lipid membranes by magic angle spinning NMR spectroscopy.

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5.  13C NMR detects conformational change in the 100-kD membrane transporter ClC-ec1.

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6.  New amino acid residue type identification experiments valid for protonated and deuterated proteins.

Authors:  David Pantoja-Uceda; Jorge Santoro
Journal:  J Biomol NMR       Date:  2012-09-04       Impact factor: 2.835

7.  Solid-state nuclear magnetic resonance (NMR) spectroscopy of human immunodeficiency virus gp41 protein that includes the fusion peptide: NMR detection of recombinant Fgp41 in inclusion bodies in whole bacterial cells and structural characterization of purified and membrane-associated Fgp41.

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8.  An economical method for producing stable-isotope labeled proteins by the E. coli cell-free system.

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9.  Electron spin density on the axial His ligand of high-spin and low-spin nitrophorin 2 probed by heteronuclear NMR spectroscopy.

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10.  Enhanced biosynthetically directed fractional carbon-13 enrichment of proteins for backbone NMR assignments.

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