Mechanisms and specificity of HIV entry into host cells

1993 ◽  
Vol 160 (2) ◽  
pp. 274
Author(s):  
F. Borek
Keyword(s):  
2020 ◽  
Vol 12 (13) ◽  
pp. 1213-1225 ◽  
Author(s):  
Shristi Pawnikar ◽  
Yinglong Miao

Background: Chemokine GPCRs play key roles in biology and medicine. Particularly, CXCR4 promotes cancer metastasis and facilitate HIV entry into host cells. Plerixafor (PLX) is a CXCR4 drug, but the pathway and binding site of PLX in CXCR4 remain unknown. Results & methodology: We have performed molecular docking and all-atom simulations using Gaussian accelerated molecular dynamics (GaMD), which are consistent with previous mutation experiments, suggesting that PLX binds to the orthosteric site of CXCR4 as an antagonist. The GaMD simulations further revealed an intermediate allosteric binding site at the extracellular mouth of CXCR4. Conclusion: The newly identified allosteric site can be targeted for novel drug design targeting CXCR4 and other chemokine receptors.


2019 ◽  
Author(s):  
Elizabeth Kruse ◽  
Tamer Abdalrahman ◽  
Philippe Selhorst ◽  
Thomas Franz

AbstractWhile HIV entry into host cells has been extensively studied from a biological and biochemical perspective, the influence of mechanical parameters of virions and cells on engulfment and invagination is not well understood. The present work aimed at developing a mathematical model to quantify effects of mechanical and morphological parameters on engulfment forces and energies of HIV particles. Invagination force and engulfment energy were described as analytical functions of radius and elastic modulus of virion and cell, ligand-receptor energy density, receptor complex density, and engulfment depth for early stage engulfment. The models were employed to study the effects of (a) virion-membrane contact geometry on required invagination force for global cell geometries and ultrastructural cell membrane features, and (b) virion radius and number of gp120 proteins on engulfment energy. The invagination force was equal for cells of various sizes (i.e. macrophages and lymphocytes), but lower when considering ultrastructural membrane. The magnitude of the normalised engulfment energy was higher for a mature than for an immature, larger virion with the same number of 72 gp120 spikes, but it decreased for a mature virion with a reduced number of gp120 spikes. The results suggest that for early stage engulfment (1) localised cell membrane features promote invagination and may play a role in entry ability, and (2) shedding of gp120 proteins during maturation reduces engulfment energy which is expected to reduce entry ability.


2017 ◽  
Vol 112 (3) ◽  
pp. 80a
Author(s):  
Sung-Tae Yang ◽  
Volker Kiessling ◽  
Lukas K. Tamm

1998 ◽  
Vol 72 (6) ◽  
pp. 5251-5255 ◽  
Author(s):  
Sujatha Iyengar ◽  
James E. K. Hildreth ◽  
David H. Schwartz

ABSTRACT Human immunodeficiency virus (HIV) envelope binds CD4 and a chemokine receptor in sequence, releasing hydrophobic viral gp41 residues into the target membrane. HIV entry required actin-dependent concentration of coreceptors, which could be disrupted by cytochalasin D (CytoD) without an effect on cell viability or mitosis. Pretreatment of peripheral blood mononuclear cells, but not virus, inhibited entry and infection. Immunofluorescent confocal microscopy of activated cells revealed CD4 and CXCR4 in nonoverlapping patterns. Addition of gp120 caused polarized cocapping of both molecules with subsequent pseudopod formation, while CytoD pretreatment blocked these membrane changes completely.


Author(s):  
H.M. Mazzone ◽  
W.F. Engler ◽  
G. Wray ◽  
A. Szirmae ◽  
J. Conroy ◽  
...  

Viral inclusion bodies isolated from infected pest insects are being evaluated by the U.S. Dept. of Agriculture as biological insecticides against their hosts. Our research on these inclusion bodies constitutes part of an effort to support their approval by the Environmental Protection Agency as insect control agents. The inclusion bodies in this study are polyhedral in shape and contain rod-shaped viral particles. When ingested by pest insects, the inclusion bodies are broken down in the insect gut and release the viral particles which infect and multiply in the nuclei of host cells. These viruses are termed nucleopolyhedrosis viruses (NPV) and are representatives of the baculoviruses (Wildy, P. 1971 IN J.L. Melnick, ed., Monographs in Virology, vol. 5, S.Karger, New York).


2009 ◽  
Author(s):  
Nadia Bergeron ◽  
J. Corriveau ◽  
Ann Letellier ◽  
F. Daigle ◽  
L. Lessard ◽  
...  

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