Aminooxypentane-RANTES induces CCR5 internalization but inhibits recycling: a novel inhibitory mechanism of HIV infectivity
about
Trafficking of the HIV coreceptor CXCR4. Role of arrestins and identification of residues in the c-terminal tail that mediate receptor internalizationDifferential activation of CC chemokine receptors by AOP-RANTESViral entry through CXCR4 is a pathogenic factor and therapeutic target in human immunodeficiency virus type 1 diseaseRab11-family interacting protein 2 and myosin Vb are required for CXCR2 recycling and receptor-mediated chemotaxisHsc/Hsp70 interacting protein (hip) associates with CXCR2 and regulates the receptor signaling and traffickingSpontaneous and antigen-induced production of HIV-inhibitory beta-chemokines are associated with AIDS-free statusImmuno-pathomechanism of liver fibrosis: targeting chemokine CCL2-mediated HIV:HCV nexusStructural and functional studies of the potent anti-HIV chemokine variant P2-RANTESThe BBXB motif of RANTES is the principal site for heparin binding and controls receptor selectivityNatural truncation of the chemokine MIP-1 beta /CCL4 affects receptor specificity but not anti-HIV-1 activityStructure-function relationship between the human chemokine receptor CXCR3 and its ligandsA small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activityVariable sensitivity of CCR5-tropic human immunodeficiency virus type 1 isolates to inhibition by RANTES analogsHIV-1 escape from a small molecule, CCR5-specific entry inhibitor does not involve CXCR4 useNatural proteolytic processing of hemofiltrate CC chemokine 1 generates a potent CC chemokine receptor (CCR)1 and CCR5 agonist with anti-HIV propertiesPotent, broad-spectrum inhibition of human immunodeficiency virus type 1 by the CCR5 monoclonal antibody PRO 140Identification and characterization of ZEL-H16 as a novel agonist of the histamine H3 receptorC-terminal engineering of CXCL12 and CCL5 chemokines: functional characterization by electrophysiological recordingsAnalysis of ligand-stimulated CC chemokine receptor 5 (CCR5) phosphorylation in intact cells using phosphosite-specific antibodiesPeptide and protein-based inhibitors of HIV-1 co-receptorsFlat clathrin lattices: stable features of the plasma membrane.Multiple active states and oligomerization of CCR5 revealed by functional properties of monoclonal antibodies.Human immunodeficiency virus type 1 entry inhibitors selected on living cells from a library of phage chemokines.Enhancement of the HIV-1 inhibitory activity of RANTES by modification of the N-terminal region: dissociation from CCR5 activation.A new mouse model for female genital schistosomiasis.HIV coreceptors, cell tropism and inhibition by chemokine receptor ligands.Will multiple coreceptors need to be targeted by inhibitors of human immunodeficiency virus type 1 entry?Highly potent RANTES analogues either prevent CCR5-using human immunodeficiency virus type 1 infection in vivo or rapidly select for CXCR4-using variants.Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5Chemokine receptor trafficking and viral replication.Emerging concepts and approaches for chemokine-receptor drug discovery.Use of inhibitors to evaluate coreceptor usage by simian and simian/human immunodeficiency viruses and human immunodeficiency virus type 2 in primary cells.Chemokine receptor oligomerization and allostery.Donor- and ligand-dependent differences in C-C chemokine receptor 5 reexpression.Human immunodeficiency virus type 1 (HIV-1)-induced GRO-alpha production stimulates HIV-1 replication in macrophages and T lymphocytesDifferential effects of CC chemokines on CC chemokine receptor 5 (CCR5) phosphorylation and identification of phosphorylation sites on the CCR5 carboxyl terminus.Seven transmembrane receptors as shapeshifting proteins: the impact of allosteric modulation and functional selectivity on new drug discovery.Highly potent inhibition of human immunodeficiency virus type 1 replication by TAK-220, an orally bioavailable small-molecule CCR5 antagonist.Resistance to the CCR5 inhibitor 5P12-RANTES requires a difficult evolution from CCR5 to CXCR4 coreceptor use.Simian immunodeficiency virus infection alters chemokine networks in lung tissues of cynomolgus macaques: association with Pneumocystis carinii infection.
P2860
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P2860
Aminooxypentane-RANTES induces CCR5 internalization but inhibits recycling: a novel inhibitory mechanism of HIV infectivity
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Aminooxypentane-RANTES induces ...... y mechanism of HIV infectivity
@en
Aminooxypentane-RANTES induces ...... mechanism of HIV infectivity.
@nl
type
label
Aminooxypentane-RANTES induces ...... y mechanism of HIV infectivity
@en
Aminooxypentane-RANTES induces ...... mechanism of HIV infectivity.
@nl
prefLabel
Aminooxypentane-RANTES induces ...... y mechanism of HIV infectivity
@en
Aminooxypentane-RANTES induces ...... mechanism of HIV infectivity.
@nl
P2093
P2860
P356
P1476
Aminooxypentane-RANTES induces ...... y mechanism of HIV infectivity
@en
P2093
Clapham PR
Proudfoot AE
Schlöndorff D
Signoret N
Stangassinger M
P2860
P304
P356
10.1084/JEM.187.8.1215
P407
P577
1998-04-01T00:00:00Z