4.3 Article

Low-E probe for 19F-1H NMR of dilute biological solids

Journal

JOURNAL OF MAGNETIC RESONANCE
Volume 189, Issue 2, Pages 182-189

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jmr.2007.09.008

Keywords

RF sample heating; fluorine NMR; membrane proteins; dielectric loss; loop-gap resonator; flat coil probe; solid state NMR probe; low-E; LGR; Alderman-Grant

Funding

  1. NIGMS NIH HHS [P01 GM64676] Funding Source: Medline

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Sample heating induced by radio frequency (RF) irradiation presents a significant challenge to solid state NMR experiments in proteins and other biological systems, causing the sample to dehydrate which may result in distorted spectra and a damaged sample. In this work we describe a large volume, low-E F-19-H-1 solid state NMR probe, which we developed for the 2D F-19 CPMG studies of dilute membrane proteins in a static and electrically lossy environment at 600 MHz field. In (19)FCPMG and related multi-pulse F-19-H-1 experiments the sample is heated by the conservative electric fields E produced in the sample coil at both F-19 and H-1 frequencies. Instead of using a traditional sample solenoid, our low-E F-19-H-1 probe utilizes two orthogonal loop-gap resonators in order to minimize the conservative electric fields responsible for sample heating. Absence of the wavelength effects in loop-gap resonators results in homogeneous RF fields and enables the study of large sample volumes, an important feature for the dilute protein preparations. The orthogonal resonators also provide intrinsic isolation between the F-19 and H-1 channels, which is another major challenge for the F-19-H-1 circuits where Larmor frequencies are only 6% apart. We detail steps to reduce 19F background signals from the probe, which included careful choice of capacitor lubricants and manufacture of Custom non-fluorinated coaxial cables. Application of the probe for two-dimensional F-19 CPMG spectroscopy in oriented lipid membranes is demonstrated with Flufenamic acid (FFA), a non-steroidal anti-inflammatory drug. (c) 2007 Elsevier Inc. All rights reserved.

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