Literature DB >> 9172743

Influence of lipid chain unsaturation on melittin-induced micellization.

M Monette1, M Lafleur.   

Abstract

It is well known that melittin, an amphipathic helical peptide, causes the micellization of phosphatidylcholine vesicles. In the present work, we conclude that the extent of micellization is dependent on the level of unsaturation of the lipid acyl chains. We report the results obtained on two systems: dipalmitoylphosphatidylcholine (DPPC), containing 10(mol)% saturated or unsaturated fatty acid (palmitic, oleic, or linoleic), and DPPC, containing 10(mol)% positively charged diacyloxy-3-(trimethylammonio)propane bearing palmitic or oleic acyl chains. For both systems, the presence of unsaturation in the lipid acyl chains inhibits melittin-induced micellization. Conversely, the addition of saturated palmitic acid to the DPPC matrix enhances the micellization. This modulation is proposed to be associated with the cohesion of the hydrophobic core. When the lipid chain packing of the gel-phase bilayer is already perturbed by the presence of unsaturation, it seems easier for the membrane to accommodate melittin at the interface, and the distribution of the peptide in the bilayer could be the origin of the inhibition of the micellization. The cohesion of the apolar core is shown to play an unquestionable role in melittin-induced micellization; however, this contribution does not appear to be as important as the electrostatic interactions between melittin and positively or negatively charged lipids.

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Year:  1996        PMID: 9172743      PMCID: PMC1225194          DOI: 10.1016/S0006-3495(96)79785-0

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  26 in total

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Authors:  J Seelig
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Authors:  E Habermann
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4.  Effects of tumbling and lateral diffusion on phosphatidylcholine model membrane 31P-NMR lineshapes.

Authors:  E E Burnell; P R Cullis; B de Kruijff
Journal:  Biochim Biophys Acta       Date:  1980-12-02

5.  Action of melittin on the DPPC-cholesterol liquid-ordered phase: a solid state 2H-and 31P-NMR study.

Authors:  T Pott; E J Dufourc
Journal:  Biophys J       Date:  1995-03       Impact factor: 4.033

6.  Physicochemical studies of the protein-lipid interactions in melittin-containing micelles.

Authors:  J Lauterwein; C Bösch; L R Brown; K Wüthrich
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7.  Modulation of melittin-induced lysis by surface charge density of membranes.

Authors:  M Monette; M Lafleur
Journal:  Biophys J       Date:  1995-01       Impact factor: 4.033

8.  The effect of free fatty acids on the thermotropic phase transition of dimyristoyl glycerophosphocholine.

Authors:  J R Usher; R M Epand; D Papahadjopoulos
Journal:  Chem Phys Lipids       Date:  1978-10       Impact factor: 3.329

9.  Incorporation of saturated fatty acids into phosphatidylcholine bilayers.

Authors:  S Mabrey; J M Sturtevant
Journal:  Biochim Biophys Acta       Date:  1977-03-25

10.  Differential thermal analysis of dipalmitoylphosphatidylcholine--fatty acid mixtures.

Authors:  S E Schullery; T A Seder; D A Weinstein; D A Bryant
Journal:  Biochemistry       Date:  1981-11-24       Impact factor: 3.162

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  8 in total

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2.  Melittin-lipid bilayer interactions and the role of cholesterol.

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3.  Composition effect on peptide interaction with lipids and bacteria: variants of C3a peptide CNY21.

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4.  Melittin-Induced Lipid Extraction Modulated by the Methylation Level of Phosphatidylcholine Headgroups.

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5.  The lipid dependence of melittin action investigated by dual-color fluorescence burst analysis.

Authors:  Geert van den Bogaart; Jacek T Mika; Victor Krasnikov; Bert Poolman
Journal:  Biophys J       Date:  2007-04-13       Impact factor: 4.033

6.  Sizing membrane pores in lipid vesicles by leakage of co-encapsulated markers: pore formation by melittin.

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Journal:  Biophys J       Date:  1997-04       Impact factor: 4.033

7.  The activity of the amphipathic peptide delta-lysin correlates with phospholipid acyl chain structure and bilayer elastic properties.

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Review 8.  Mechanistic Landscape of Membrane-Permeabilizing Peptides.

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