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19F Paramagnetic Relaxation-Based NMR for Quaternary Structural Restraints of Ion Channels.


ABSTRACT: Quaternary distance restraints are essential to define the three-dimensional structures of protein assemblies. These distances often fall within a range of 10-18 Å, which challenges the high and low measurement limits of conventional nuclear magnetic resonance (NMR) and double electron-electron resonance electron spin resonance spectroscopies. Here, we report the use of 19F paramagnetic relaxation enhancement (PRE) NMR in combination with 19F/paramagnetic labeling to equivalent sites in different subunits of a protein complex in micelles to determine intersubunit distances. The feasibility of this strategy was evaluated on a pentameric ligand-gated ion channel, for which we found excellent agreement of the 19F PRE NMR results with previous structural information. The study suggests that 19F PRE NMR is a viable tool in extracting distance restraints to define quaternary structures.

SUBMITTER: Bondarenko V 

PROVIDER: S-EPMC7092367 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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<sup>19</sup>F Paramagnetic Relaxation-Based NMR for Quaternary Structural Restraints of Ion Channels.

Bondarenko Vasyl V   Wells Marta M MM   Chen Qiang Q   Singewald Kevin C KC   Saxena Sunil S   Xu Yan Y   Tang Pei P  

ACS chemical biology 20190918 10


Quaternary distance restraints are essential to define the three-dimensional structures of protein assemblies. These distances often fall within a range of 10-18 Å, which challenges the high and low measurement limits of conventional nuclear magnetic resonance (NMR) and double electron-electron resonance electron spin resonance spectroscopies. Here, we report the use of <sup>19</sup>F paramagnetic relaxation enhancement (PRE) NMR in combination with <sup>19</sup>F/paramagnetic labeling to equiva  ...[more]

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