نتایج جستجو برای: v3

تعداد نتایج: 5209  

2012
Masaru Yokoyama Satoshi Naganawa Kazuhisa Yoshimura Shuzo Matsushita Hironori Sato

BACKGROUND The net charge of the hypervariable V3 loop on the HIV-1 envelope gp120 outer domain plays a key role in modulating viral phenotype. However, the molecular mechanisms underlying the modulation remain poorly understood. METHODOLOGY/PRINCIPAL FINDINGS By combining computational and experimental approaches, we examined how V3 net charge could influence the phenotype of the gp120 inter...

Journal: :Journal of virology 1993
K Holmbäck P Kusk E F Hulgaard T H Bugge E Scheibel B O Lindhardt

High titers of neutralizing antibodies in human immunodeficiency virus type 1 (HIV-1) infection are directed primarily against the third hypervariable domain (V3) of the virion envelope glycoprotein gp120. This region has been designated the principal neutralizing domain of HIV-1. Because the frequency and significance of autologous V3 antibodies in natural infection are not fully clarified, we...

2010
Catarina E. Hioe Terri Wrin Michael S. Seaman Xuesong Yu Blake Wood Steve Self Constance Williams Miroslaw K. Gorny Susan Zolla-Pazner

BACKGROUND The V3 loop of the HIV-1 envelope (Env) glycoprotein gp120 was identified as the "principal neutralizing domain" of HIV-1, but has been considered too variable to serve as a neutralizing antibody (Ab) target. Structural and immunochemical data suggest, however, that V3 contains conserved elements which explain its role in binding to virus co-receptors despite its sequence variability...

2013
Yuzhe Yuan Masaru Yokoyama Yosuke Maeda Hiromi Terasawa Shinji Harada Hironori Sato Keisuke Yusa

Maraviroc, an (HIV-1) entry inhibitor, binds to CCR5 and efficiently prevents R5 human immunodeficiency virus type 1 (HIV-1) from using CCR5 as a coreceptor for entry into CD4(+) cells. However, HIV-1 can elude maraviroc by using the drug-bound form of CCR5 as a coreceptor. This property is known as noncompetitive resistance. HIV-1(V3-M5) derived from HIV-1(JR-FLan) is a noncompetitive-resistan...

Journal: :Virology 2013
Raiees Andrabi Constance Williams Xiao-Hong Wang Liuzhe Li Alok K Choudhary Naveet Wig Ashutosh Biswas Kalpana Luthra Arthur Nadas Michael S Seaman Phillipe Nyambi Susan Zolla-Pazner Miroslaw K Gorny

One approach to the development of an HIV vaccine is to design a protein template which can present gp120 epitopes inducing cross-neutralizing antibodies. To select a V3 sequence for immunogen design, we compared the neutralizing activities of 18 anti-V3 monoclonal antibodies (mAbs) derived from Cameroonian and Indian individuals infected with clade AG and C, respectively. It was found that V3 ...

Journal: :Odontología Activa Revista Científica 2018

Journal: :Journal of virology 1993
P N Nehete R B Arlinghaus K J Sastry

Because V3 loop-specific antibodies have been shown to inhibit human immunodeficiency virus type 1 (HIV-1) infection of human cells and because specific mutations in the V3 loop render the virus ineffective for infection and syncytium formation, we tested the anti-HIV effects of V3 loop peptides from different HIV-1 strains. We obtained evidence that V3 loop synthetic peptides of 8 to 15 amino ...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2013
Joanna Borowska Christopher T Jones Han Zhang Jake Blacklaws Martyn Goulding Ying Zhang

V3 interneurons (INs) are a major group of excitatory commissural interneurons in the spinal cord, and they are essential for producing a stable and robust locomotor rhythm. V3 INs are generated from the ventral-most progenitor domain, p3, but migrate dorsally and laterally during postmitotic development. At birth, they are located in distinctive clusters in the ventral horn and deep dorsal hor...

Journal: :Journal of virology 2009
Katie L Davis Frederic Bibollet-Ruche Hui Li Julie M Decker Olaf Kutsch Lynn Morris Aidy Salomon Abraham Pinter James A Hoxie Beatrice H Hahn Peter D Kwong George M Shaw

Deciphering antibody specificities that constrain human immunodeficiency virus type 1 (HIV-1) envelope (Env) diversity, limit virus replication, and contribute to neutralization breadth and potency is an important goal of current HIV/AIDS vaccine research. Transplantation of discrete HIV-1 neutralizing epitopes into HIV-2 scaffolds may provide a sensitive, biologically functional context by whi...

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