|
|
||||||||
Journal of Lipid Research, Vol 28, 710-718, Copyright © 1987 by Lipid Research, Inc.
PK Sripada, PR Maulik, JA Hamilton and GG Shipley
A series of sphingomyelins (SM) with different chain length fatty acids
(C14:0, C16:0, C18:0, C20:0, C22:0, and C24:0) N-linked to the primary
amino group of sphingosine have been synthesized starting with bovine brain
SM. Two different acid hydrolysis procedures, butanolic HCl (H. Kaller,
1961. Biochem. Z. 334: 451-456) and methanolic HCl (R.C. Gaver and C.C.
Sweeley. 1965. J. Am. Oil Chem. Soc. 42: 294-298), were used and the
resultant sphingosylphosphocholine (SPC) was converted to SM using two
acylation methods: using fatty acid imidazolide to yield the O-acyl, N-acyl
SPC, followed by mild alkaline hydrolysis for selective deacylation at the
O-acyl linkage, and selective acylation at the amino group of SPC using the
free fatty acid in the presence of dicyclohexylcarbodimide. Following
chromatographic purification, N-acyl SM were obtained in high yield
(80-90%), and were characterized by a combination of thin-layer
chromatography, high performance liquid chromatography, chemical analysis,
optical rotation, circular dichroism, infrared spectroscopy, 13C NMR, and
sphingosine base analysis. The N-acyl SM were chemically homogeneous with
respect to fatty acid composition and the sphingosine base composition
resembled that of the starting bovine brain SM. However, as a consequence
of the epimerization at C-3 of SPC in both acid hydrolysis procedures, the
resulting N-acyl SM consisted of mixtures of D-erythro and L-threo
sphingomyelins. By differential scanning calorimetry hydrated C14:0 to
C24:0 SM exhibited gel-liquid crystal transitions in the range 30-50
degrees C but the chain length dependence was complex.(ABSTRACT TRUNCATED
AT 250 WORDS)
ARTICLES
Partial synthesis and properties of a series of N-acyl sphingomyelins
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
P. S. Niemela, M. T. Hyvonen, and I. Vattulainen Influence of Chain Length and Unsaturation on Sphingomyelin Bilayers Biophys. J., February 1, 2006; 90(3): 851 - 863. [Abstract] [Full Text] [PDF] |
||||
![]() |
M.-L. Wong, B. Xie, N. Beatini, P. Phu, S. Marathe, A. Johns, P. W. Gold, E. Hirsch, K. J. Williams, J. Licinio, et al. Acute systemic inflammation up-regulates secretory sphingomyelinase in vivo: A possible link between inflammatory cytokines and atherogenesis PNAS, July 5, 2000; (2000) 150098097. [Abstract] [Full Text] |
||||
![]() |
X. Buton, Z. Mamdouh, R. Ghosh, H. Du, G. Kuriakose, N. Beatini, G. A. Grabowski, F. R. Maxfield, and I. Tabas Unique Cellular Events Occurring during the Initial Interaction of Macrophages with Matrix-retained or Methylated Aggregated Low Density Lipoprotein (LDL). PROLONGED CELL-SURFACE CONTACT DURING WHICH LDL-CHOLESTERYL ESTER HYDROLYSIS EXCEEDS LDL PROTEIN DEGRADATION J. Biol. Chem., November 5, 1999; 274(45): 32112 - 32121. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Marathe, G. Kuriakose, K. J. Williams, and I. Tabas Sphingomyelinase, an Enzyme Implicated in Atherogenesis, Is Present in Atherosclerotic Lesions and Binds to Specific Components of the Subendothelial Extracellular Matrix Arterioscler. Thromb. Vasc. Biol., November 1, 1999; 19(11): 2648 - 2658. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. L. Schissel, G. A. Keesler, E. H. Schuchman, K. J. Williams, and I. Tabas The Cellular Trafficking and Zinc Dependence of Secretory and Lysosomal Sphingomyelinase, Two Products of the Acid Sphingomyelinase Gene J. Biol. Chem., July 17, 1998; 273(29): 18250 - 18259. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Marathe, S. L. Schissel, M. J. Yellin, N. Beatini, R. Mintzer, K. J. Williams, and I. Tabas Human Vascular Endothelial Cells Are a Rich and Regulatable Source of Secretory Sphingomyelinase. IMPLICATIONS FOR EARLY ATHEROGENESIS AND CERAMIDE-MEDIATED CELL SIGNALING J. Biol. Chem., February 13, 1998; 273(7): 4081 - 4088. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. L. Schissel, X.-c. Jiang, J. Tweedie-Hardman, T.-s. Jeong, E. H. Camejo, J. Najib, J. H. Rapp, K. J. Williams, and I. Tabas Secretory Sphingomyelinase, a Product of the Acid Sphingomyelinase Gene, Can Hydrolyze Atherogenic Lipoproteins at Neutral pH. IMPLICATIONS FOR ATHEROSCLEROTIC LESION DEVELOPMENT J. Biol. Chem., January 30, 1998; 273(5): 2738 - 2746. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. L. Schissel, E. H. Schuchman, K. J. Williams, and I. Tabas Zn2+-stimulated Sphingomyelinase Is Secreted by Many Cell Types and Is a Product of the Acid Sphingomyelinase Gene J. Biol. Chem., August 2, 1996; 271(31): 18431 - 18436. [Abstract] [Full Text] [PDF] |
||||
![]() |
M.-L. Wong, B. Xie, N. Beatini, P. Phu, S. Marathe, A. Johns, P. W. Gold, E. Hirsch, K. J. Williams, J. Licinio, et al. Acute systemic inflammation up-regulates secretory sphingomyelinase in vivo: A possible link between inflammatory cytokines and atherogenesis PNAS, July 18, 2000; 97(15): 8681 - 8686. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Journal of Biological Chemistry |
| Molecular and Cellular Proteomics | ASBMB Today |