Determination of Long-Range Distances by Fast Magic-Angle-Spinning Radiofrequency-Driven 19F-19F Dipolar Recoupling NMR

摘要

Nanometer-range distances are important for restraining the three-dimensional structure and oligomeric assembly of proteins and other biological molecules. Solid-state NMR determination of protein structures typically utilizes ¹³C–¹³C and ¹³C–¹⁵N distance restraints, which can only be measured up to ~7 Å due to the low gyromagnetic ratios of these nuclear spins. To extend the distance reach of NMR, one can harvest the power of ¹⁹F, whose large gyromagnetic ratio in principle allows distances up to 2 nm to be measured. However, ¹⁹F possesses large chemical shift anisotropies (CSAs) as well as large isotropic chemical shift dispersions, which pose challenges to dipolar coupling measurements. Here we demonstrate ¹⁹F–¹⁹F distance measurements at high magnetic fields under fast magic-angle spinning (MAS) using radiofrequency-driven dipolar recoupling (RFDR). We show that ¹⁹F–¹⁹F cross peaks for distances up to 1 nm can be readily observed in 2D ¹⁹F–¹⁹F correlation spectra using less than 5 ms of RFDR mixing. This efficient ¹⁹F–¹⁹F dipolar recoupling is achieved using practically accessible MAS frequencies of 15–55 kHz, moderate ¹⁹F rf field strengths, and no ¹H decoupling. Experiments and simulations show that the fastest polarization transfer for aromatic fluorines with the highest distance accuracy is achieved using either fast MAS (e.g. 60 kHz) with large pulse duty cycles (> 50%) or slow MAS with strong ¹⁹F pulses. Fast MAS considerably reduces relaxation losses during the RFDR π-pulse train, making finite-pulse RFDR under fast-MAS the method of choice. Under intermediate MAS frequencies (25–40 kHz) and intermediate pulse duty cycles (15–30%), the ¹⁹F CSA tensor orientation has a quantifiable effect on the polarization transfer rate, thus the RFDR buildup curves encode both distance and orientation information. At fast MAS, the impact of CSA orientation is minimized, allowing pure distance restraints to be extracted. We further investigate how relayed transfer and dipolar truncation in multi-fluorine environments affect polarization transfer. This fast-MAS ¹⁹F RFDR approach is complementary to ¹⁹F spin diffusion for distance measurements, and will be the method of choice under high-field fast-MAS conditions that are increasingly important for protein structure determination by solid-state NMR.