Isotope labeling methods for studies of excited protein states by relaxation dispersion NMR spectroscopy

被引:0
|
作者
Patrik Lundström
Pramodh Vallurupalli
D Flemming Hansen
Lewis E Kay
机构
[1] Chemistry and Biology,Division of Molecular Biotechnology, Department of Physics
[2] Linköping University,Departments of Molecular Genetics
[3] Biochemistry and Chemistry,undefined
[4] The University of Toronto,undefined
来源
Nature Protocols | 2009年 / 4卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The utility of nuclear magnetic resonance (NMR) spectroscopy as a tool for the study of biomolecular structure and dynamics has benefited from the development of facile labeling methods that incorporate NMR active probes at key positions in the molecule. Here we describe a protocol for the labeling of proteins that facilitates their study using a technique that is sensitive to millisecond conformational exchange processes. The samples necessary for an analysis of exchange dynamics are discussed, using the Abp1p SH3 domain from Saccharomyces cerevisiae as an example. For this system, the time frame for production of each sample, including in vitro refolding, is about 80 h. The samples so produced facilitate the measurement of accurate chemical shifts of low populated, invisible conformers that are part of the exchange pathway. The accuracy of the methodology has been established experimentally and the chemical shifts that are obtained provide important restraints in structure calculations of the excited state.
引用
收藏
页码:1641 / 1648
页数:7
相关论文
共 50 条
  • [1] Isotope labeling methods for studies of excited protein states by relaxation dispersion NMR spectroscopy
    Lundstroem, Patrik
    Vallurupalli, Pramodh
    Hansen, D. Flemming
    Kay, Lewis E.
    NATURE PROTOCOLS, 2009, 4 (11) : 1641 - 1648
  • [2] Structures of invisible, excited protein states by relaxation dispersion NMR spectroscopy
    Vallurupalli, Pramodh
    Hansen, D. Flemming
    Kay, Lewis E.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (33) : 11766 - 11771
  • [3] Stable isotope labeling methods for protein NMR spectroscopy
    Ohki, Shin-Ya
    Kainosho, Masatsune
    PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2008, 53 (04) : 208 - 226
  • [4] Using relaxation dispersion NMR spectroscopy to determine structures of excited, invisible protein states
    Hansen, D. Flemming
    Vallurupalli, Pramodh
    Kay, Lewis E.
    JOURNAL OF BIOMOLECULAR NMR, 2008, 41 (03) : 113 - 120
  • [5] Using relaxation dispersion NMR spectroscopy to determine structures of excited, invisible protein states
    D. Flemming Hansen
    Pramodh Vallurupalli
    Lewis E. Kay
    Journal of Biomolecular NMR, 2008, 41 : 113 - 120
  • [6] Accurate measurement of alpha proton chemical shifts of excited protein states by relaxation dispersion NMR spectroscopy
    Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada
    J. Am. Chem. Soc., 2009, 5 (1915-1926):
  • [7] Accurate Measurement of Alpha Proton Chemical Shifts of Excited Protein States by Relaxation Dispersion NMR Spectroscopy
    Lundstroem, Patrik
    Hansen, D. Flemming
    Vallurupalli, Pramodh
    Kay, Lewis E.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (05) : 1915 - 1926
  • [8] Excited States of Nucleic Acids Probed by Proton Relaxation Dispersion NMR Spectroscopy
    Juen, Michael Andreas
    Wunderlich, Christoph Hermann
    Nussbaumer, Felix
    Tollinger, Martin
    Kontaxis, Georg
    Konrat, Robert
    Hansen, D. Flemming
    Kreutz, Christoph
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (39) : 12008 - 12012
  • [9] Relaxation Dispersion NMR Spectroscopy as a Tool for Detailed Studies of Protein Folding
    Neudecker, Philipp
    Lundstrom, Patrik
    Kay, Lewis E.
    BIOPHYSICAL JOURNAL, 2009, 96 (06) : 2045 - 2054
  • [10] Measurement of methyl axis orientations in invisible, excited states of proteins by relaxation dispersion NMR spectroscopy
    Baldwin, Andrew J.
    Hansen, D. Flemming
    Vallurupalli, Pramodh
    Kay, Lewis E.
    Journal of the American Chemical Society, 2009, 131 (33): : 11939 - 11948