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NMR analysis of in vitro-synthesized proteins without purification: a high-throughput approach
Faculty of Science, Medicine and Health - Papers
  • Laurent Guignard, Australian National University
  • Kiyoshi Ozawa, University of Wollongong
  • Sharon E Pursglove, Australian National University
  • Gottfried Otting, Australian National University
  • Nicholas E Dixon, University of Wollongong
RIS ID
16965
Publication Date
1-1-2002
Publication Details

Guignard, L., Ozawa, K., Pursglove, S. E., Otting, G. & Dixon, N. E. (2002). NMR analysis of in vitro-synthesized proteins without purification: a high-throughput approach. FEBS Letters, 524 (1-3), 159-162.

Abstract

A cell-free protein expression system was established that provides protein samples of adequate concentration and purity for direct NMR analysis. The Escherichia coli peptidyl–prolyl cistrans isomerase PpiB was expressed in this system with dual amino acid-selective isotope labeling to identify the NMR signal from the active site-residue Arg87. Addition of the substrate succinyl-Ala-Ala-Pro-Phe-p-nitroanilide selectively shifted its 15N-HSQC cross peak, confirming binding to the active site. As cell-free protein expression provides high yields of protein per unit mass of labeled amino acid and sample handling is minimal, this strategy presents an exceptionally inexpensive and rapid approach to protein analysis.

Citation Information
Laurent Guignard, Kiyoshi Ozawa, Sharon E Pursglove, Gottfried Otting, et al.. "NMR analysis of in vitro-synthesized proteins without purification: a high-throughput approach" (2002)
Available at: http://works.bepress.com/nick_dixon/27/