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Colloids and Surfaces B: Biointerfaces
Volume 41, Issue 1, 10 March 2005, Pages 15-20
 
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doi:10.1016/j.colsurfb.2004.10.026    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2004 Elsevier B.V. All rights reserved.

Cooperative effects in phospholipid monolayers induced by a peptide from HIV-1 capsid protein

Marli L. Moraesa, Cláudia Bonardia, Cleber R. Mendonçaa, Patrícia T. Campanaa, Javier Lottersbergerb, Georgina Tonarellib, Osvaldo N. Oliveira, Jr.a, Corresponding Author Contact Information, E-mail The Corresponding Author and Leila M. Beltraminia

aInstituto de Física de São Carlos, USP, CP 369, 13560-970 São Carlos, Brazil bFacultad de Bioquímica y Cs. Biológicas, Departamento de Química Orgánica, Santa Fé, Argentina

Received 28 October 2004; 
accepted 28 October 2004. 
Available online 15 December 2004.

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Abstract

The study of interactions between biological molecules and model membranes is essential for the understanding of a number of physiological mechanisms involved in viral infections and dissemination. In this paper, the analysis of the interaction between a peptide from the p24 protein of Human Immunodeficiency Virus type 1 (HIV-1) and a phospholipid monolayer has pointed to a cooperative response in which very small amounts of peptide p24-1 (e.g. 0.05 mol%) can lead to measurable effects. Monolayer surface pressure and surface potential isotherms were affected for peptide concentrations as low as 0.05 mol%, with saturation at 0.5 mol%. The expansion effect from p24-1 is confirmed by changes in morphology of the monolayers using Brewster angle microscopy. Even though p24-1 is disordered in aqueous solutions, the interaction with dipalmitoyl phosphatidylcholine (DPPC) causes it to adopt an α-helix structure, as shown by circular dichroism (CD) data for multilamellar vesicles (MLV). The expansion of the phospholipid monolayer in a cooperative way may imply that p24-1 has potential antiviral activity, by participating in the cell rupture, with no need of specific receptors in the membrane.

Keywords: Phospholipid monolayer; HIV-1 peptide; Brewster angle microscopy; Circular dichroism; Multilamellar vesicles

Article Outline

1. Introduction
2. Materials and methods
2.1. Lipids and peptide
2.2. Langmuir monolayers
2.3. Multilamellar vesicles
2.4. Secondary structure prediction
3. Results and discussion
Acknowledgements
References







 
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