Literature DB >> 17762877

Solution NMR of supramolecular complexes: providing new insights into function.

Remco Sprangers1, Algirdas Velyvis, Lewis E Kay.   

Abstract

Solution NMR spectroscopy is an extremely powerful technology for the study of biomolecular dynamics and site-specific molecular interactions. An important limitation in the past has been molecule size, with molecular weights of targets seldom exceeding 50 kDa. New labeling technology and NMR experiments are changing this paradigm so that applications for investigating supramolecular complexes are starting to become feasible. Here we describe a strategy developed in our laboratory that involves the use of labeled methyl groups of isoleucine, leucine and valine residues in proteins as probes, along with experiments that significantly enhance the lifetimes of the resulting signals. We describe the application of these methods to a number of systems with molecular weights in the hundreds of kilodaltons.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17762877     DOI: 10.1038/nmeth1080

Source DB:  PubMed          Journal:  Nat Methods        ISSN: 1548-7091            Impact factor:   28.547


  63 in total

1.  Estimating side-chain order in methyl-protonated, perdeuterated proteins via multiple-quantum relaxation violated coherence transfer NMR spectroscopy.

Authors:  Hechao Sun; Raquel Godoy-Ruiz; Vitali Tugarinov
Journal:  J Biomol NMR       Date:  2012-03       Impact factor: 2.835

2.  Long-range interaction networks in the function and fidelity of poliovirus RNA-dependent RNA polymerase studied by nuclear magnetic resonance.

Authors:  Xiaorong Yang; Jesse L Welch; Jamie J Arnold; David D Boehr
Journal:  Biochemistry       Date:  2010-11-02       Impact factor: 3.162

3.  The proteasome antechamber maintains substrates in an unfolded state.

Authors:  Amy M Ruschak; Tomasz L Religa; Sarah Breuer; Susanne Witt; Lewis E Kay
Journal:  Nature       Date:  2010-10-14       Impact factor: 49.962

4.  Efficient segmental isotope labeling of multi-domain proteins using Sortase A.

Authors:  Lee Freiburger; Miriam Sonntag; Janosch Hennig; Jian Li; Peijian Zou; Michael Sattler
Journal:  J Biomol NMR       Date:  2015-08-30       Impact factor: 2.835

5.  Structural basis for signal-sequence recognition by the translocase motor SecA as determined by NMR.

Authors:  Ioannis Gelis; Alexandre M J J Bonvin; Dimitra Keramisanou; Marina Koukaki; Giorgos Gouridis; Spyridoula Karamanou; Anastassios Economou; Charalampos G Kalodimos
Journal:  Cell       Date:  2007-11-16       Impact factor: 41.582

6.  Independent valine and leucine isotope labeling in Escherichia coli protein overexpression systems.

Authors:  Roman J Lichtenecker; Katharina Weinhäupl; Lukas Reuther; Julia Schörghuber; Walther Schmid; Robert Konrat
Journal:  J Biomol NMR       Date:  2013-11       Impact factor: 2.835

7.  Synthesis, characterization and applications of a perdeuterated amphipol.

Authors:  Fabrice Giusti; Jutta Rieger; Laurent J Catoire; Shuo Qian; Antonio N Calabrese; Thomas G Watkinson; Marina Casiraghi; Sheena E Radford; Alison E Ashcroft; Jean-Luc Popot
Journal:  J Membr Biol       Date:  2014-03-21       Impact factor: 1.843

8.  Monitoring protein conformational changes and dynamics using stable-isotope labeling and mass spectrometry.

Authors:  Alem W Kahsai; Sudarshan Rajagopal; Jinpeng Sun; Kunhong Xiao
Journal:  Nat Protoc       Date:  2014-05-08       Impact factor: 13.491

9.  Structural basis for protein antiaggregation activity of the trigger factor chaperone.

Authors:  Tomohide Saio; Xiao Guan; Paolo Rossi; Anastassios Economou; Charalampos G Kalodimos
Journal:  Science       Date:  2014-05-09       Impact factor: 47.728

10.  Selective 1H- 13C NMR spectroscopy of methyl groups in residually protonated samples of large proteins.

Authors:  Chenyun Guo; Vitali Tugarinov
Journal:  J Biomol NMR       Date:  2009-12-03       Impact factor: 2.835

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.