2018
DOI: 10.2217/fvl-2017-0114
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HIV Antivirals: Targeting the Functional Organization of the Lipid Envelope

Abstract: Most of the surface of the lipid bilayer covering the human immunodeficiency virus type 1 (HIV-1) particle is directly accessible from the aqueous medium. Its peculiar chemical composition and physical properties appear to be critical for infection and, therefore, may comprise a target for selective antiviral activity. The HIV-1 membrane is enriched in raft-type lipids and also displays aminophospholipids on its external leaflet. We contend here that a great deal of membrane-active compounds described to block… Show more

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Cited by 6 publications
(5 citation statements)
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“…These results suggested that the HIV membrane constitutes a functional viral component during entry. In line with this hypothesis, different membrane-targeting compounds present antiviral activity, as reviewed in [16] and [17].…”
Section: Introductionmentioning
confidence: 73%
See 1 more Smart Citation
“…These results suggested that the HIV membrane constitutes a functional viral component during entry. In line with this hypothesis, different membrane-targeting compounds present antiviral activity, as reviewed in [16] and [17].…”
Section: Introductionmentioning
confidence: 73%
“…Many membrane-targeting compounds have been shown to inhibit -or promote -HIV-1 fusion, suggesting that the viral membrane constitutes a functional element of the entry process [16,17]. Still, the exact role of lipids during HIV-1 entry is unknown [38].…”
Section: Imaging Lipids During Hiv Entrymentioning
confidence: 99%
“…Another mediator of HIV cell entry has been described; the phosphatidylserine exposed on the viral membrane can interact with host phosphatidylserine-binding molecules [ 63 ]. However, while membrane-active compounds could inhibit HIV-1 cell entry and display virucidal activity, they face the same challenges as all lipophilic antivirals, a lack of specificity and high cell toxicity [ 64 ].…”
Section: Viral and Host Factors Modulating Hiv-1 Entrymentioning
confidence: 99%
“…Although these interactions often imply the presence of membrane receptors, some bioactive amphiphilic molecules directly interact with the lipid matrix of membranes [1][2][3]. Among these, two main classes of molecules, rhamnolipids and lipopeptides, have been the subjects of several studies reporting the crucial role of the biomolecule-lipid phase interactions for their antimicrobial activities (for examples see: [2,[4][5][6][7][8][9]). While the mechanism is well described for some biological activities of these membrane-active molecules [10,11], for other bioactivities such as plant immunity stimulation by rhamnolipids [12] or lipopeptides [13][14][15], or their antifungal activities [6,16], the mechanism is still elusive.…”
Section: Introductionmentioning
confidence: 99%