Bringing dynamic molecular machines into focus by methyl-TROSY NMR
- PMID: 24905784
- DOI: 10.1146/annurev-biochem-060713-035829
Bringing dynamic molecular machines into focus by methyl-TROSY NMR
Abstract
Large macromolecular assemblies, so-called molecular machines, are critical to ensuring proper cellular function. Understanding how proper function is achieved at the atomic level is crucial to advancing multiple avenues of biomedical research. Biophysical studies often include X-ray diffraction and cryo-electron microscopy, providing detailed structural descriptions of these machines. However, their inherent flexibility has complicated an understanding of the relation between structure and function. Solution NMR spectroscopy is well suited to the study of such dynamic complexes, and continued developments have increased size boundaries; insights into function have been obtained for complexes with masses as large as 1 MDa. We highlight methyl-TROSY (transverse relaxation optimized spectroscopy) NMR, which enables the study of such large systems, and include examples of applications to several cellular machines. We show how this emerging technique contributes to an understanding of cellular function and the role of molecular plasticity in regulating an array of biochemical activities.
Keywords: allostery; deuteration; high–molecular weight complexes; methyl labeling; protein NMR; protein–substrate interactions.
Similar articles
-
Solution NMR spectroscopy of supra-molecular systems, why bother? A methyl-TROSY view.J Magn Reson. 2011 Jun;210(2):159-70. doi: 10.1016/j.jmr.2011.03.008. Epub 2011 Mar 8. J Magn Reson. 2011. PMID: 21458338
-
TROSY NMR spectroscopy of large soluble proteins.Top Curr Chem. 2013;335:97-119. doi: 10.1007/128_2011_228. Top Curr Chem. 2013. PMID: 21928013 Review.
-
TROSY in NMR studies of the structure and function of large biological macromolecules.Curr Opin Struct Biol. 2003 Oct;13(5):570-80. doi: 10.1016/j.sbi.2003.09.009. Curr Opin Struct Biol. 2003. PMID: 14568611 Review.
-
Exploring long-range cooperativity in the 20S proteasome core particle from Thermoplasma acidophilum using methyl-TROSY-based NMR.Proc Natl Acad Sci U S A. 2020 Mar 10;117(10):5298-5309. doi: 10.1073/pnas.1920770117. Epub 2020 Feb 24. Proc Natl Acad Sci U S A. 2020. PMID: 32094174 Free PMC article.
-
NMR techniques used with very large biological macromolecules in solution.Methods Enzymol. 2005;394:382-98. doi: 10.1016/S0076-6879(05)94015-9. Methods Enzymol. 2005. PMID: 15808229
Cited by
-
13C NMR detects conformational change in the 100-kD membrane transporter ClC-ec1.J Biomol NMR. 2015 Apr;61(3-4):209-26. doi: 10.1007/s10858-015-9898-7. Epub 2015 Jan 29. J Biomol NMR. 2015. PMID: 25631353 Free PMC article.
-
Oligomeric assembly regulating mitochondrial HtrA2 function as examined by methyl-TROSY NMR.Proc Natl Acad Sci U S A. 2021 Mar 16;118(11):e2025022118. doi: 10.1073/pnas.2025022118. Proc Natl Acad Sci U S A. 2021. PMID: 33692127 Free PMC article.
-
Visualizing Conformational Ensembles of the Nucleosome by NMR.ACS Chem Biol. 2022 Mar 18;17(3):495-502. doi: 10.1021/acschembio.1c00954. Epub 2022 Feb 23. ACS Chem Biol. 2022. PMID: 35196453 Free PMC article. Review.
-
Reversible inhibition of the ClpP protease via an N-terminal conformational switch.Proc Natl Acad Sci U S A. 2018 Jul 10;115(28):E6447-E6456. doi: 10.1073/pnas.1805125115. Epub 2018 Jun 25. Proc Natl Acad Sci U S A. 2018. PMID: 29941580 Free PMC article.
-
Distortion of histone octamer core promotes nucleosome mobilization by a chromatin remodeler.Science. 2017 Jan 20;355(6322):eaaa3761. doi: 10.1126/science.aaa3761. Science. 2017. PMID: 28104838 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
