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

被引:11
作者
Bondarenko, Vasyl [1 ]
Wells, Marta [1 ]
Chen, Qiang [1 ]
Singewald, Kevin C. [6 ]
Saxena, Sunil [6 ]
Xu, Yan [1 ,3 ,4 ,5 ]
Tang, Pei [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Dept Anesthesiol & Perioperat Med, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Computat & Syst Biol, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Dept Struct Biol, Pittsburgh, PA 15260 USA
[5] Univ Pittsburgh, Dept Phys & Astron, Pittsburgh, PA 15260 USA
[6] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
关键词
DISTANCE MEASUREMENTS; PROTEIN-STRUCTURE; ENHANCEMENT; RESONANCE; CONFORMATIONS; REVEALS; STATES;
D O I
10.1021/acschembio.9b00692
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Quaternary distance restraints are essential to define the three-dimensional structures of protein assemblies, These distances often fall within a range of 10-18 angstrom, which challenges the high and low measurement limits of conventional nuclear magnetic resonance (NMR) and double r electron-electron resonance electron spin resonance spectroscopies. Here, we report the use of F-19 paramagnetic relaxation enhancement (PRE) NMR in combination with F-19/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 F-19 PRE NMR results with previous structural information. The study suggests that F-19 PRE NMR is a viable tool in extracting distance restraints to define quaternary structures.
引用
收藏
页码:2160 / 2165
页数:6
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