Investigation into the Acyl Chain Packing of Endotoxins and Phospholipids under Near Physiological Conditions by WAXS and FTIR Spectroscopy

The acyl chain packing of various endotoxins and phospholipids was monitored via the main wideangle reflection between 0.410 and 0.460 nm by wide-angle X-ray scattering (WAXS) and via the absorption band of the symmetric stretching vibration of the methylene groups vs(CH2) around 2849 to 2853 cm−1 b...

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Published inJournal of structural biology Vol. 128; no. 2; pp. 175 - 186
Main Authors Brandenburg, K., Funari, S.S., Koch, M.H.J., Seydel, U.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.12.1999
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Abstract The acyl chain packing of various endotoxins and phospholipids was monitored via the main wideangle reflection between 0.410 and 0.460 nm by wide-angle X-ray scattering (WAXS) and via the absorption band of the symmetric stretching vibration of the methylene groups vs(CH2) around 2849 to 2853 cm−1 by Fourier-transform infrared spectroscopy. The lipids investigated included various rough mutant (R) and smooth form (S) lipopolysaccharides (LPS) differing in the length of the sugar portion, lipid A, the “endotoxic principle” of LPS, and various saturated and unsaturated phospholipids with different head groups under a near physiological (≥85%) water content. The packing density of the saturated endotoxin acyl chains is lower than those of saturated phospholipids but similar to those of monounsaturated phospholipids, each in the gel phase. The hydrophobic moiety of endotoxins thus exhibits significant conformational disorder already in the gel phase. The acyl chain packing of the endotoxins decreases with increasing length of the sugar chain lengths, which seems to be relevant to the observed differences in biological activity. For Re-LPS with different counterions (salt forms), in the presence of externally added cations or at reduced water content (50%), no change of the acyl chain packing density is deduced in the X-ray data, although the FT-IR data indicate its increase. The position of the vs(CH2) vibration is, thus, only a relative measure of lipid order, in particular when lipids with different head groups and in the presence of external agents are compared.
AbstractList The acyl chain packing of various endotoxins and phospholipids was monitored via the main wide-angle reflection between 0.410 and 0.460 nm by wide-angle X-ray scattering (WAXS) and via the absorption band of the symmetric stretching vibration of the methylene groups v(s)(CH(2)) around 2849 to 2853 cm(-1) by Fourier-transform infrared spectroscopy. The lipids investigated included various rough mutant (R) and smooth form (S) lipopolysaccharides (LPS) differing in the length of the sugar portion, lipid A, the "endotoxic principle" of LPS, and various saturated and unsaturated phospholipids with different head groups under a near physiological (>/=85%) water content. The packing density of the saturated endotoxin acyl chains is lower than those of saturated phospholipids but similar to those of monounsaturated phospholipids, each in the gel phase. The hydrophobic moiety of endotoxins thus exhibits significant conformational disorder already in the gel phase. The acyl chain packing of the endotoxins decreases with increasing length of the sugar chain lengths, which seems to be relevant to the observed differences in biological activity. For Re-LPS with different counterions (salt forms), in the presence of externally added cations or at reduced water content (50%), no change of the acyl chain packing density is deduced in the X-ray data, although the FT-IR data indicate its increase. The position of the v(s)(CH(2)) vibration is, thus, only a relative measure of lipid order, in particular when lipids with different head groups and in the presence of external agents are compared.
The acyl chain packing of various endotoxins and phospholipids was monitored via the main wideangle reflection between 0.410 and 0.460 nm by wide-angle X-ray scattering (WAXS) and via the absorption band of the symmetric stretching vibration of the methylene groups vs(CH2) around 2849 to 2853 cm−1 by Fourier-transform infrared spectroscopy. The lipids investigated included various rough mutant (R) and smooth form (S) lipopolysaccharides (LPS) differing in the length of the sugar portion, lipid A, the “endotoxic principle” of LPS, and various saturated and unsaturated phospholipids with different head groups under a near physiological (≥85%) water content. The packing density of the saturated endotoxin acyl chains is lower than those of saturated phospholipids but similar to those of monounsaturated phospholipids, each in the gel phase. The hydrophobic moiety of endotoxins thus exhibits significant conformational disorder already in the gel phase. The acyl chain packing of the endotoxins decreases with increasing length of the sugar chain lengths, which seems to be relevant to the observed differences in biological activity. For Re-LPS with different counterions (salt forms), in the presence of externally added cations or at reduced water content (50%), no change of the acyl chain packing density is deduced in the X-ray data, although the FT-IR data indicate its increase. The position of the vs(CH2) vibration is, thus, only a relative measure of lipid order, in particular when lipids with different head groups and in the presence of external agents are compared.
The acyl chain packing of various endotoxins and phospholipids was monitored via the main wide-angle reflection between 0.410 and 0.460 nm by wide-angle X-ray scattering (WAXS) and via the absorption band of the symmetric stretching vibration of the methylene groups v(s)(CH(2)) around 2849 to 2853 cm(-1) by Fourier-transform infrared spectroscopy. The lipids investigated included various rough mutant (R) and smooth form (S) lipopolysaccharides (LPS) differing in the length of the sugar portion, lipid A, the "endotoxic principle" of LPS, and various saturated and unsaturated phospholipids with different head groups under a near physiological (>/=85%) water content. The packing density of the saturated endotoxin acyl chains is lower than those of saturated phospholipids but similar to those of monounsaturated phospholipids, each in the gel phase. The hydrophobic moiety of endotoxins thus exhibits significant conformational disorder already in the gel phase. The acyl chain packing of the endotoxins decreases with increasing length of the sugar chain lengths, which seems to be relevant to the observed differences in biological activity. For Re-LPS with different counterions (salt forms), in the presence of externally added cations or at reduced water content (50%), no change of the acyl chain packing density is deduced in the X-ray data, although the FT-IR data indicate its increase. The position of the v(s)(CH(2)) vibration is, thus, only a relative measure of lipid order, in particular when lipids with different head groups and in the presence of external agents are compared.
Author Koch, M.H.J.
Funari, S.S.
Brandenburg, K.
Seydel, U.
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– sequence: 4
  givenname: U.
  surname: Seydel
  fullname: Seydel, U.
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/10600571$$D View this record in MEDLINE/PubMed
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Keywords outer membrane
lipid A
acyl chain packing
phospholipid
WAXS
LPS
endotoxin
FTIR spectroscopy
Language English
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Snippet The acyl chain packing of various endotoxins and phospholipids was monitored via the main wideangle reflection between 0.410 and 0.460 nm by wide-angle X-ray...
The acyl chain packing of various endotoxins and phospholipids was monitored via the main wide-angle reflection between 0.410 and 0.460 nm by wide-angle X-ray...
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StartPage 175
SubjectTerms acyl chain packing
endotoxin
Endotoxins - chemistry
FTIR spectroscopy
lipid A
Lipid A - chemistry
Lipopolysaccharides - chemistry
LPS
Molecular Conformation
outer membrane
phospholipid
Phospholipids - chemistry
Salmonella
Spectroscopy, Fourier Transform Infrared
WAXS
X-Ray Diffraction
Title Investigation into the Acyl Chain Packing of Endotoxins and Phospholipids under Near Physiological Conditions by WAXS and FTIR Spectroscopy
URI https://dx.doi.org/10.1006/jsbi.1999.4186
https://www.ncbi.nlm.nih.gov/pubmed/10600571
https://search.proquest.com/docview/69364001
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