Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1988 Oct;43(4):226-34.
doi: 10.1007/BF02555139.

Modulation of calcium phosphate formation by phosphatidate-containing anionic liposomes

Affiliations

Modulation of calcium phosphate formation by phosphatidate-containing anionic liposomes

E D Eanes et al. Calcif Tissue Int. 1988 Oct.

Abstract

Liposome prepared from 7:2:1 molar mixtures of phosphatidylcholine, dicetyl phosphate, and cholesterol to which 1-20 mole % dioleoylphosphatidic acid (DOPA) was added were used to examine the effect of membrane-bound monoester phosphatidate anions on calcium phosphate formation in aqueous solutions at 22 degrees C, pH 7.4 and 240 mOsm. Results showed that up to 20 mole % DOPA in the liposomal envelope did not initiate mineralization in solutions made metastable with 2.25 mM CaCl2 and 1.50 mM KH2PO4. Results alos revealed that precipitation induced in metastable solutions by the seeding action of intraliposomally formed mineral was measurably reduced with as little as 1 mole % DOPA and completely suppressed with 5 mole % DOPA. In contrast, 10 mole % concentrations of diester phosphate lipids either had no effect on extraliposomal precipitation (e.g., phosphatidylglycerol and phosphatidylinositol) or, as reported previously for phosphatidylserine) only partially reduced the amount of precipitate formed. Transmission electron microscopical analysis suggests that DOPA-containing lipid bilayers adhering to the seed crystals inhibited extraliposomal mineralization by encapsulating the crystals within the liposomes and/or by blocking potential growth sites on the crystal faces. The polar head group of DOPA, being more negatively charged and sterically less encumbered than diester phosphate ligands, most probably was responsible for this adherence of the lipid bilayers to the crystal surfaces.

PubMed Disclaimer

References

    1. Eur J Biochem. 1967 Mar;1(1):61-9 - PubMed
    1. Biochim Biophys Acta. 1984 Nov 7;777(2):343-6 - PubMed
    1. J Biol Chem. 1982 May 10;257(9):4746-52 - PubMed
    1. J Biol Chem. 1981 Mar 25;256(6):2736-41 - PubMed
    1. J Biol Chem. 1976 Mar 10;251(5):1326-32 - PubMed

MeSH terms