4.5 Article

Phospholipids in Motion: High-Resolution 31P NMR Field Cycling Studies

期刊

JOURNAL OF PHYSICAL CHEMISTRY B
卷 125, 期 31, 页码 8827-8838

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.1c02105

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资金

  1. National Science Foundation [MCB-0950331]

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Diverse phospholipid motions were analyzed using high-resolution NMR technique, revealing different lateral diffusion constants for phospholipids in the same bilayer and the effects of additives on phospholipid motion. Additionally, it was found that polar headgroup motion of phospholipids is not restricted on a microsecond timescale.
Diverse phospholipid motions are key to membrane function but can be quite difficult to untangle and quantify. High-resolution field cycling P-31 NMR spin-lattice relaxometry, where the sample is excited at high field, shuttled in the magnet bore for low-field relaxation, then shuttled back to high field for readout of the residual magnetization, provides data on phospholipid dynamics and structure. This information is encoded in the field dependence of the P-31 spin-lattice relaxation rate (R-1). In the field range from 11.74 down to 0.003 T, three dipolar nuclear magnetic relaxation dispersions (NMRDs) and one due to P-31 chemical shift anisotropy contribute to R1 of phospholipids. Extraction of correlation times and maximum relaxation amplitudes for these NMRDs provides (1) lateral diffusion constants for different phospholipids in the same bilayer, (2) estimates of how additives alter the motion of the phospholipid about its long axis, and (3) an average P-31-H-1 angle with respect to the bilayer normal, which reveals that polar headgroup motion is not restricted on a microsecond timescale. Relative motions within a phospholipid are also provided by comparing P-31 NMRD profiles for specifically deuterated molecules as well as C-13 and H-1 field dependence profiles to that of P-31. Although this work has dealt exclusively with phospholipids in small unilamellar vesicles, these same NMRDs can be measured for phospholipids in micelles and nanodisks, making this technique useful for monitoring lipid behavior in a variety of structures and assessing how additives alter specific lipid motions.

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