Literature DB >> 26651836

Solution NMR Spectroscopy Provides an Avenue for the Study of Functionally Dynamic Molecular Machines: The Example of Protein Disaggregation.

Rina Rosenzweig1, Lewis E Kay1,2.   

Abstract

Solution-based NMR spectroscopy has been an important tool for studying the structure and dynamics of relatively small proteins and protein complexes with aggregate molecular masses under approximately 50 kDa. The development of new experiments and labeling schemes, coupled with continued improvements in hardware, has significantly reduced this size limitation, enabling atomic-resolution studies of molecular machines in the 1 MDa range. In this Perspective, some of the important advances are highlighted in the context of studies of molecular chaperones involved in protein disaggregation. New insights into the structural biology of disaggregation obtained from NMR studies are described, focusing on the unique capabilities of the methodology for obtaining atomic-resolution descriptions of dynamic systems.

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Year:  2015        PMID: 26651836     DOI: 10.1021/jacs.5b11346

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  4 in total

1.  Unfolding the mechanism of the AAA+ unfoldase VAT by a combined cryo-EM, solution NMR study.

Authors:  Rui Huang; Zev A Ripstein; Rafal Augustyniak; Michal Lazniewski; Krzysztof Ginalski; Lewis E Kay; John L Rubinstein
Journal:  Proc Natl Acad Sci U S A       Date:  2016-07-11       Impact factor: 11.205

2.  An intrinsically disordered motif regulates the interaction between the p47 adaptor and the p97 AAA+ ATPase.

Authors:  Alexander E Conicella; Rui Huang; Zev A Ripstein; Ai Nguyen; Eric Wang; Thomas Löhr; Peter Schuck; Michele Vendruscolo; John L Rubinstein; Lewis E Kay
Journal:  Proc Natl Acad Sci U S A       Date:  2020-10-07       Impact factor: 11.205

3.  NMR characterization of HtpG, the E. coli Hsp90, using sparse labeling with 13C-methyl alanine.

Authors:  Kari Pederson; Gordon R Chalmers; Qi Gao; Daniel Elnatan; Theresa A Ramelot; Li-Chung Ma; Gaetano T Montelione; Michael A Kennedy; David A Agard; James H Prestegard
Journal:  J Biomol NMR       Date:  2017-06-26       Impact factor: 2.835

4.  Unraveling self-assembly pathways of the 468-kDa proteolytic machine TET2.

Authors:  Pavel Macek; Rime Kerfah; Elisabetta Boeri Erba; Elodie Crublet; Christine Moriscot; Guy Schoehn; Carlos Amero; Jerome Boisbouvier
Journal:  Sci Adv       Date:  2017-04-07       Impact factor: 14.136

  4 in total

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