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Phospholipase cleavage of D- and L-chiro-glycosylphosphoinositides asymmetrically incorporated into liposomal membranes
- Source :
- Digital.CSIC. Repositorio Institucional del CSIC, instname
- Publication Year :
- 2005
-
Abstract
- 16 páginas, 3 figuras, 1 tabla, 3 esquemas.<br />The nature of chiro-inositol-containing inositolphosphoglycans (IPGs), reported to be putative insulin mediators, was studied by examination of the substrate specificities of the phosphatidylinositol-specific phospholipase C (PI-PLC) and the glycosylphosphatidylinositol-specific phospholipase D (GPI-PLD) by using a series of synthetic D- and L-chiro-glycosylphosphoinositides. 3-O-α-D-Glucosaminyl- (3) and -galactosaminyl-2-phosphatidyl-L-chiro-inositol (4), which show the maximum stereochemical similarity to the 6-O-α-D-glucosaminylphosphatidylinositol pseudodisaccharide motifs of GPI anchors, were synthesized and asymmetrically incorporated into phospholipid bilayers in the form of large unilamellar vesicles (LUVs). Similarly, 2-O-α-D-glucosaminyl- (5) and -galactosaminyl-1-phosphatidyl-D-chiro-inositol (6), which differ from the corresponding pseudodisaccharide motif of the GPI anchors only in the axial orientation of the phosphatidyl moiety, were also synthesized and asymmetrically inserted into LUVs. The cleavage of these synthetic molecules in the liposomal constructs by PI-PLC from Bacillus cereus and by GPI-PLD from bovine serum was studied with the use of 6-O-α-D-glucosaminylphosphatidylinositol (7) and the conserved GPI anchor structure (8) as positive controls. Although PI-PLC cleaved 3 and 4 with about the same efficiency as 7 and 8, this enzyme did not accept 5 or 6. GPI-PLD accepted both the L-chiro- (3 and 4) and the D-chiro- (5 and 6) glycosylinositolphosphoinositides. Therefore, IPGs containing L-chiro-inositol only are expected to be released from chiro-inositol-containing GPIs if the cleavage is effected by a PI-PLC, whereas GPI-PLD cleavage could result in both L-chiro- and D-chiro-inositol-containing IPGs.<br />We thank the Dirección General de Investigación for financial support (Grants BQU 2002–03734 and BFU 2004–02955), Dr. J. López-Prados and F. Alfonso for providing samples of 8, and 31 and 32, respectively, and the Ministerio de Educación y Ciencia for a Ramón y Cajal contract (to M.B.C.).
- Subjects :
- Stereochemistry
Glycosylphosphatidylinositols
Lipid Bilayers
Phospholipid
Phospholipase
Glycophosphoinositides
Cleavage (embryo)
Catalysis
chemistry.chemical_compound
Glycolipid
Phosphoinositide Phospholipase C
Phosphoinositide phospholipase C
Bovine serum albumin
Phospholipids
Liposome
biology
Phospholipase C
Molecular Structure
Phospholipase D
Chemistry
Vesicle
Phosphatidylinositol Diacylglycerol-Lyase
Organic Chemistry
General Chemistry
General Medicine
Membrane
Phospholipases
Type C Phospholipases
Liposomes
biology.protein
lipids (amino acids, peptides, and proteins)
Glycolipids
Inositols
Subjects
Details
- ISSN :
- 09476539
- Volume :
- 12
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Chemistry (Weinheim an der Bergstrasse, Germany)
- Accession number :
- edsair.doi.dedup.....e11dbc81459c52d4771c2b036ead2194