Abstract
X-ray diffraction is used to solve the low-resolution structures of fully hydrated aqueous dispersions of seven different diacyl phosphatidylethanolamines (PEs) whose hydrocarbon chains have the same effective chain length but whose structures vary widely. Both the lower-temperature, liquid-crystalline lamellar (L(alpha)) and the higher-temperature, inverted hexagonal (H(II)) phase structures are solved, and the resultant internal dimensions (d-spacing, water layer thickness, average lipid length, and headgroup area at the lipid-water interface) of each phase are determined as a function of temperature. The magnitude of the L(alpha) and H(II) phase d-spacings on either side of the L(alpha)/H(II) phase transition temperature (T(h)) depends significantly on the structure of the PE hydrocarbon chains. The L(alpha) phase d-spacings range from 51.2 to 56.4 A, whereas those of the H(II) phase range from 74.9 to 82.7 A. These new results differ from our earlier measurements of these PEs (Lewis et al., Biochemistry, 28:541-548, 1989), which found near constant d-spacings of 52.5 and 77.0-78.0 A for the L(alpha) and H(II) phases, respectively. In both phases, the d-spacings decrease with increasing temperature independent of chain structure, but, in both phases, the rate of decrease in the L(alpha) phase is smaller than that in the H(II) phase. A detailed molecular description of the L(alpha)/H(II) phase transition in these PEs is also presented.
Full Text
The Full Text of this article is available as a PDF (736.9 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Lewis R. N., Mannock D. A., McElhaney R. N., Turner D. C., Gruner S. M. Effect of fatty acyl chain length and structure on the lamellar gel to liquid-crystalline and lamellar to reversed hexagonal phase transitions of aqueous phosphatidylethanolamine dispersions. Biochemistry. 1989 Jan 24;28(2):541–548. doi: 10.1021/bi00428a020. [DOI] [PubMed] [Google Scholar]
- Mariani P., Rivas E., Luzzati V., Delacroix H. Polymorphism of a lipid extract from Pseudomonas fluorescens: structure analysis of a hexagonal phase and of a novel cubic phase of extinction symbol Fd--. Biochemistry. 1990 Jul 24;29(29):6799–6810. doi: 10.1021/bi00481a007. [DOI] [PubMed] [Google Scholar]
- Melchior D. L., Scavitto F. J., Steim J. M. Dilatometry of dipalmitoyllecithin-cholesterol bilayers. Biochemistry. 1980 Oct 14;19(21):4828–4834. doi: 10.1021/bi00562a018. [DOI] [PubMed] [Google Scholar]
- Nagle J. F., Wilkinson D. A. Lecithin bilayers. Density measurement and molecular interactions. Biophys J. 1978 Aug;23(2):159–175. doi: 10.1016/S0006-3495(78)85441-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- So PT, Gruner SM, Erramilli S. Pressure-induced topological phase transitions in membranes. Phys Rev Lett. 1993 May 31;70(22):3455–3458. doi: 10.1103/PhysRevLett.70.3455. [DOI] [PubMed] [Google Scholar]
- Stamatoff J. B., Krimm S. Phase determination of x-ray reflections for membrane-type systems with constant fluid density. Biophys J. 1976 May;16(5):503–516. doi: 10.1016/S0006-3495(76)85705-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tate M. W., Gruner S. M. Temperature dependence of the structural dimensions of the inverted hexagonal (HII) phase of phosphatidylethanolamine-containing membranes. Biochemistry. 1989 May 16;28(10):4245–4253. doi: 10.1021/bi00436a019. [DOI] [PubMed] [Google Scholar]
- Turner D. C., Gruner S. M. X-ray diffraction reconstruction of the inverted hexagonal (HII) phase in lipid-water systems. Biochemistry. 1992 Feb 11;31(5):1340–1355. doi: 10.1021/bi00120a009. [DOI] [PubMed] [Google Scholar]
- Wiener M. C., White S. H. Structure of a fluid dioleoylphosphatidylcholine bilayer determined by joint refinement of x-ray and neutron diffraction data. III. Complete structure. Biophys J. 1992 Feb;61(2):434–447. doi: 10.1016/S0006-3495(92)81849-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yang C. P., Wiener M. C., Lewis R. N., McElhaney R. N., Nagle J. F. Dilatometric studies of isobranched phosphatidylcholines. Biochim Biophys Acta. 1986 Dec 1;863(1):33–44. doi: 10.1016/0005-2736(86)90384-6. [DOI] [PubMed] [Google Scholar]