Fourier transform infrared spectroscopy of aqueous dispersions of phosphatidylserine-cholesterol mixtures
β Scribed by V. Brumfeld; D. Bach; I. R. Miller
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 657 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1432-1017
No coin nor oath required. For personal study only.
β¦ Synopsis
The effect of cholesterol on vibrational spectra in the non polar and in the polar region of dimyristoyl phosphatidylserine (DMPS) and of phosphatidylserine from bovine spinal cord (PS) has been investigated. The small shifts in the methylene CH stretching frequencies after taking into account the contribution of the cholesterol spectrum were interpreted as a combined effect of cholesterol on the conformation of the chains and of the lesser contributions of the cholesterol methyl groups. Cholesterol also influences the ratio of the trans (1465 cm-1) to the lower wavelength (1457 cm-1) CH2 bending bands. No significant direct effect of cholesterol on the vibration of the polar residues was discerned. The small shift of the carboxylate band observed below the phase transition is probably due to the change in the intermolecular zwitterions when the average distance between the neighboring polar groups increases due to incorporation of cholesterol molecules.
π SIMILAR VOLUMES
Near-infrared (NIR) spectroscopy has been extensively and successfully used in food industries, but it has never been widely used in the chemical industry or chemical laboratories. For process and quality control measurements, NIR spectroscopy, with the development of new, rugged, reliable technique
Modern protein Fourier transform infrared (FT-IR) spectroscopy has proven to be a versatile and sensitive technique, applicable to many aspects of protein characterization. The major practical drawback for the FT-IR spectroscopy of proteins is the large absorbance band of water, which overlaps the a
The infrared vibration-rotation bands of SeH have been measured in the X 2 βΈ ground state using a Fourier transform spectrometer. The bands were observed in a microwave discharge of a mixture of H 2 and Se in the presence of He. The rotational structure of the 1-0, 2-1, 3-2 bands of the X 2 βΈ 3/ 2 s