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A study of HIV-1 FP inhibition by GBV-C peptides using lipid nano-assemblies

•P 45 GBV-C peptide inhibits HIV-1 FP activity at membrane level in vitro.•P45+HIV-1 FP mixture produces dissolution of lipid condensed domains at high pressure.•AFM reveals arrowhead structures when P45 peptide interact with DMPC:DMPS (3:2) film. Langmuir–Blodgett films (LBs) and supported lipid bi...

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Published in:Colloids and surfaces. A, Physicochemical and engineering aspects Physicochemical and engineering aspects, 2015-09, Vol.480, p.184-190
Main Authors: Ortiz, Alba, Domènech, Oscar, Muñoz-Juncosa, Montserrat, Prat, Josefina, Haro, Isabel, Girona, Victoria, Alsina, M. Asunción, Pujol, Montserrat
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Language:English
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Summary:•P 45 GBV-C peptide inhibits HIV-1 FP activity at membrane level in vitro.•P45+HIV-1 FP mixture produces dissolution of lipid condensed domains at high pressure.•AFM reveals arrowhead structures when P45 peptide interact with DMPC:DMPS (3:2) film. Langmuir–Blodgett films (LBs) and supported lipid bilayers (SLBs) of dimyristoylphosphatidylcholine (DMPC)–dimyristoylphosphatidylserine (DMPS) (3:2) were used to investigate the way that a GBV-C peptide (P45) inhibits the immunodeficiency human virus fusion peptide (HIV-1 FP) action at membrane level. Supported lipid bilayers (SLBs) were prepared by direct adsorption of a liposomal dispersion on solid mica slides and Langmuir–Blodgett films (LBs) by a deposition of a monolayer onto mica solid surface at different compression pressures. The behaviour of P45, HIV-1 FP and a mixture of P45 and HIV-1 FP (1:1) were monitored in the two phospholipid membrane models by fluorescence microscopy (FM) and atomic force microscopy (AFM). Experiments with SLBs confirmed that P45 inhibited HIV-1 FP action in vitro. LBs obtained at 10 and 25mNm−1 confirmed different lipid interactions for DMPC/DMPS (3:2) in combination with either P45 (8:2), HIV-1 FP (8:2), or P45 and HIV-1 FP (8:1:1). The P45 peptide was confirmed to modulate the action of HIV-1 FP. Furthermore, FM and AFM images showed that HIV-1 FP had a pressure-independent membrane-level behaviour when compared with P45 and the P45+HIV-1 FP (1:1) mixture. This mixture also had dramatic effects on the appearance of liquid expanded (LE)–liquid condensed (LC) phase coexistence as shown by FM and AFM.
ISSN:0927-7757
1873-4359
DOI:10.1016/j.colsurfa.2014.12.048