Experiment OP - 10.1021/ja029029o/1

Article DOI 10.1021/ja029029o
Data DOI N/A
Internal ID 10.1021/ja029029o/1
Membrane composition (molar fraction)
SDPC 1-stearyl-2-docosahexaenoyl-sn-glycero-3-phosphocholine 1
Solution composition Pure water
Temperature (K) 303.15
Total hydration 50 (mass %)
pH UNKNOWN
Reagent sources
SDPC (d3518:0)-SDPC was synthesized by Avanti Polar lipids.
water Carefully degassed, deuterium-depleted water or D2O (Cambridge Isotope Laboratories, Woburn, MA)
Sample protocol lipid/water dispersions were homogenized by stirring and centrifugation and then packed
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Name Value
DATE 2003-05-21 05:48:00
ADDITIONAL_MOLECULES
Key Value
DTPA diethylenetriaminepentaacetic acid, 1 mM
BHT 2,6-di-tert-butyl-4-methylphenol, 1:150 (bht:lipid)
NMR
Key Value
T_RF_HEATING measured
INSTRUMENT Bruker DMX500 and DMX300, 4mm MAS probe
METHOD 2H:QE, 13C:INVREC/CP
SIGN_MEASURED NONE
DETAILS Deuterium NMR spectra were observed at 46.1 MHz using a quadrupolar echo pulse sequence (d1-90°x-τ-90°y-acquire) with a repetition time d1=0.5s, a 2.7-μs 90° pulse, a delay time τ=50μs, and a spectral width of 200kHz. T1 were measured at a MAS spinning frequency of 10 kHz by the inversion−recovery pulse sequence (d1-180°-τ-90°-acquire), a delay time d1=11.5s, a 5.5-μs 90° pulse, and a spectral width of 27.7kHz. The experiments were conducted with 50 kHz of proton noise decoupling during data acquisition. The 13C NMR cross-polarization experiments were conducted at a MAS spinning frequency of 5kHz using a shaped spin-lock pulse that increments the carbon spin-lock field strength from 20kHz to 25kHz in 10 steps. 24 The spin-lock field strength for 1H resonances was adjusted to achieve maximum signal intensity using an adamantane sample. Signal intensity of lipid samples was recorded as a function of contact time over the range from 100 μs to 300 ms. Order parameter for 13C-1H was estimated form CP magnetization transfer as described in the manuscript.

Order Parameters SDPC

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