Literature DB >> 28686451

Revival of the Intermolecular Nuclear Overhauser Effect for Mapping Local Protein Hydration Dynamics.

Daniel Braun1, Michael Schmollngruber1, Othmar Steinhauser1.   

Abstract

The highly heterogeneous hydration dynamics of protein-water interfaces is considered important for protein stability and dynamics, protein folding, enzymatic activity, and even drug design. The nuclear Overhauser effect (NOE) between protein and water protons is the only experimental observable which, in principle, can provide a map of locally resolved hydration dynamics. However, its utility was questioned in various theoretical studies that emphasized the contributions of long-range NOE interactions. We show by a detailed analysis based on molecular dynamics simulations that, contrary to recent claims, the protein-water NOE is an excellent observable to map local hydration dynamics at the protein surface.

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Year:  2017        PMID: 28686451     DOI: 10.1021/acs.jpclett.7b01013

Source DB:  PubMed          Journal:  J Phys Chem Lett        ISSN: 1948-7185            Impact factor:   6.475


  3 in total

1.  Characterizing Protein Hydration Dynamics Using Solution NMR Spectroscopy.

Authors:  Christine Jorge; Bryan S Marques; Kathleen G Valentine; A Joshua Wand
Journal:  Methods Enzymol       Date:  2018-12-04       Impact factor: 1.600

2.  Mapping temperature-dependent conformational change in the voltage-sensing domain of an engineered heat-activated K+ channel.

Authors:  Hongbo Chen; Jiahua Deng; Qiang Cui; Baron Chanda; Katherine Henzler-Wildman
Journal:  Proc Natl Acad Sci U S A       Date:  2021-04-06       Impact factor: 11.205

3.  Changes in protein hydration dynamics by encapsulation or crowding of ubiquitin: strong correlation between time-dependent Stokes shift and intermolecular nuclear Overhauser effect.

Authors:  Philipp Honegger; Esther Heid; Stella Schmode; Christian Schröder; Othmar Steinhauser
Journal:  RSC Adv       Date:  2019-11-13       Impact factor: 4.036

  3 in total

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