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1.
Dehydration reduces the main phase transition pressure of phospholipids. An analysis based on the Gibbs-Duhem equation shows how the shift of the transition pressure is correlated to the hydration pressure.By using Fourier transform infrared (FT-IR) spectroscopy we determined the hydration-dependent phase transition pressure. The application of our new approach gives hydration pressure values which agree with the values obtained with the osmotic stress method. 相似文献
2.
The synthesis and characterization of rare-earth (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu and Y) thiocyanate adducts with tripiperidinophosphine oxide (tpppO) with general formula (RE)(SCN)3(tpppO)3 are reported. Conductance measurements in acetonitrile indicate the non-electrolytic nature of the complexes. Infrared absorption spectra evidence that the SCN− ion coordinates through the nitrogen atom (isothiocyanate form) and that tpppO coordinates through the phosphoryl oxygen. X-ray powder patterns suggest the existence of three different crystal forms: (1) La; (2) an isomorphous series including Ce, Nd and Pr; and (3) another isomorphous series, including Sm, Gd, Eu, Ho, Er, Tb, Lu and Y. The visible spectra of the Nd adduct and the calculated parameters β = 0.98, b1/2 = 0.072 and δ = 1.06 indicate that the metal-ligand bonds are essentially electrostactic. The emission spectra of the Eu compound showed 5D0 → 7FJ bands (J = 0, 1, 2), suggesting a C3v symmetry for the coordination polyhedron. The lifetime of the 5D0 state is 1.28 ms. The emission spectra of the Tb complex presented 5D4 → 7FJ bands (J = 4, 5, 6) and the Dy complex showed the 4F9/2 → 6H13/2 band. The structure of the Pr complex showed that the coordination polyhedron is a trigonal antiprism, with the isothiocyanate anions in one base and three tpppO ligands in the other. Thermal analyses (TG-DTG) were carried out for the Ce, Nd and Gd adducts. Mass losses start between 250 and 334 °C. The final residues at 1300 °C are the corresponding phosphates. 相似文献
3.
P. L. Hope E. B. Cady D. T. Delpy N. K. Ives R. M. Gardiner E. O. R. Reynolds 《Journal of neurochemistry》1988,50(5):1394-1402
Brain metabolism and intracellular pH were studied during and after episodes of incomplete cerebral ischaemia in lambs under sodium pentobarbitone anaesthesia. 31P and 1H magnetic resonance spectroscopy was used to monitor brain pHi and brain concentrations of inorganic phosphate (Pi), phosphocreatine (PCr), beta-nucleoside triphosphate (beta NTP), and lactate. Simultaneous measurements were made of arterio-cerebral venous concentration differences (AVDs) for oxygen, glucose, and lactate. Cerebral ischaemia was induced by a combination of bilateral carotid clamping and hypotension, and the acute effects of systemic administration of glucose and sodium bicarbonate were examined. The molar ratio of glucose to oxygen uptake by the brain (6G/O2) increased above unity during cerebral ischaemia. Statistically significant AVDs for lactate were not observed. Cerebral ischaemia was associated with a reduction in brain pHi PCr/Pi ratio, and an increase in brain lactate. No effect of arterial plasma glucose on brain lactate concentration or brain pHi was evident during cerebral ischaemia or in the postischaemic period. Administration of sodium bicarbonate systemically in the postischaemic period was associated with a rise in arterial and brain tissue PCO2. A fall in brain pHi occurred which was attributable in part to coincidental brain lactate accumulation. The increase in brain lactate measured by 1H nuclear magnetic resonance in vivo during ischaemia was insufficient to account for the change in buffer base calculated to have occurred from previous estimates of brain buffering capacity. 相似文献
4.
Protochlorophyll (PChl) forms were performed in Triton X-100 detergent micelles. The concentration of Triton X-100 was 7·10?4 M (above the critical micellar concentration); the concentration of PChl varied between 1.6·10?5 and 1.8·10?4 M. Absorption, fluorescence and circular dichroism (CD) spectra were registered. The absorption spectra were resolved into Gaussian components by computer analysis. PChl forms with absorption bands at 632–634, 638, 652–654, 663–664, 668 and 676 nm and with fluorescence emission bands at 634–636, 640–644, 652–655, 677–678, 686 and 694–696 nm were observed in micellar solutions of different PChl concentrations. The CD spectra showed a strong dependence on the concentration of PChl: positive CD signals or positive Cotton effects were observed in the vicinity of 650 nm. The intensity of these signals increased in parallel with increasing concentration of PChl. No CD signals were found in the region of the longer wavelength absorption bands. These data show that the PChl exists in many different forms in this system, and the spectroscopic properties of these forms are determined by different molecular interactions viz., interactions of PChl with Triton X-100 or water molecules and/or by the aggregation of PChl. 相似文献
5.
6.
To study the reliabiliity of formulas for calculating mean skin temperature (T
sk), values were computed by 18 different techniques and were compared with the mean of 10,841 skin temperatures measured by
infrared thermography. One hundred whole-body infrared thermograms were scanned in ten resting males while changing the air
temperature from 40° C to 4° C. Local, regional average and mean skin temperatures were obtained using an image processing
system. The agreement frequency, defined as the percentage of the calculated T
sk values which agreed with the corresponding infrared thermographic T
sk within ±0.2° C, ranged for with the various formulas from 7% to 80%. In many sites, the local skin temperature did not coincide
with the regional average skin temperature. When the local skin temperatures which showed the highest percentage similarity
to the regional average skin temperature within ±0.4° C were applied to the formula, the agreement frequency was markedly
improved for all formulas. However, the agreement frequency was not affected by changing the weighting factors from specific
constants to individually measured values of regional surface area. By applying the physiologically reliable accuracy range
of ±0.2° C in the moderate and ±0.4° C in the cool condition, agreement frequencies of at least 95% were observed in formulas
involving seven or more skin temperature measurement sites, including the hand and foot. We conclude that calculation of a
reliable mean skin temperature must involve more than seven skin temperature measurement sites regardless of ambient temperature.
Optimal sites for skin temperature measurement are proposed for various formulas.
Received: 2 December 1996 / Accepted: 25 June 1997 相似文献
7.
Summary Conformational preferences of secretin as a model peptide have been analyzed by CD and IR spectroscopy in reverse micelles of AOT/isooctane/water and compared to those in aqueous TFE, in SDS micelles and in DMPG vesicles. Among the systems examined, reverse micelles and phospholipid vesicles displayed almost identical conformational equilibria. Very high lipid-to-peptide ratios can be obtained in reverse micelles with full retention of optical transparency, even at millimolar peptide concentrations, thus indicating this system to be an interesting mimic of cell membrane environments for spectroscopic analysis of bioactive peptide conformations.Abbreviations TFE
trifluoroethanol
- SDS
sodium dodecyl sulfate
- DMPG
dimyristoylphosphatidylglycerol
- AOT
bis(2-ethylhexyl)sulfosuccinate
- CMC
critical micellar concentration
- VIP
vasoactive intestinal peptide 相似文献
8.
9.
R.Douglas Carter Robert E. Hardy Kilian Dill 《International journal of biological macromolecules》1984,6(3):164-166
The 13C resonances of Nα,N-[13C]dimethylserine of partially 13C reductively methylated glycophorin AM were monitored as a function of pH at 45°C. For comparison, limited data are also presented for the pH dependence of the 13C resonances of Nα,N- [13C]dimethylserine of fully 13C reductively methylated deglycosylated glycophorin AM. The ‘major’ component of Nα,N- [13C]dimethylserine of glycophorin AM did not titrate, whereas the ‘minor’ component titrated with a pKa of 7.80 (Hill coefficient of 0.95). Similar results are also indicated for the Nα,N- [13C]dimethylserine resonances of 13C reductively methylated deglycosylated glycophorin AM. 相似文献
10.