نتایج جستجو برای: gp41

تعداد نتایج: 1630  

Journal: :BioTechniques 1997
R Grabherr W Ernst O Doblhoff-Dier M Sara H Katinger

Based on the method of direct cloning into the baculovirus genome by linearizing and re-ligation in presence of the target insert, we designed viral constructs that express foreign genes on the surface of baculovirus particles. We chose the glycosylated envelope protein gp41 of human immunodeficiency virus type 1 (HIV-1) as a model for displaying recombinant proteins on budded virus. The ectodo...

Journal: :Journal of virology 2010
Brett D Welch J Nicholas Francis Joseph S Redman Suparna Paul Matthew T Weinstock Jacqueline D Reeves Yolanda S Lie Frank G Whitby Debra M Eckert Christopher P Hill Michael J Root Michael S Kay

The HIV gp41 N-trimer pocket region is an ideal viral target because it is extracellular, highly conserved, and essential for viral entry. Here, we report on the design of a pocket-specific D-peptide, PIE12-trimer, that is extraordinarily elusive to resistance and characterize its inhibitory and structural properties. D-peptides (peptides composed of D-amino acids) are promising therapeutic age...

Journal: :AIDS research and human retroviruses 2000
C Yang F Gao P N Fonjungo L Zekeng G van der Groen D Pieniazek C Schable R B Lal

The molecular diversity and phylogenetic relationship of 22 HIV-1 group O strains were examined on the basis of the protease gene and the N-terminal region of gp41env. Analysis of the newly characterized protease sequences with 12 reference sequences revealed no specific clustering patterns, despite the distinct geographic locations of the specimens. In contrast, analysis of the newly sequenced...

2014
Bin Hu Hua-Xin Liao S. Munir Alam Byron Goldstein

A few broadly neutralizing antibodies, isolated from HIV-1 infected individuals, recognize epitopes in the membrane proximal external region (MPER) of gp41 that are transiently exposed during viral entry. The best characterized, 4E10 and 2F5, are polyreactive, binding to the viral membrane and their epitopes in the MPER. We present a model to calculate, for any antibody concentration, the proba...

Journal: :Virology 2009
Elena Gustchina John M Louis Christian Frisch Francisco Ylera Annette Lechner Carole A Bewley G Marius Clore

Previously we reported a broadly HIV-1 neutralizing mini-antibody (Fab 3674) of modest potency that was derived from a human non-immune phage library by panning against the chimeric gp41-derived construct N(CCG)-gp41. This construct presents the N-heptad repeat of the gp41 ectodomain as a stable, helical, disulfide-linked trimer that extends in helical phase from the six-helix bundle of gp41. I...

Journal: :Molecular medicine 1999
D C Adamson J C McArthur T M Dawson V L Dawson

BACKGROUND Fifteen to thirty percent of AIDS patients develop some type of neurologic disorder during the course of their illness and the vast majority of these neurologic disorders will be HIV-associated dementia (HAD). These patients can exhibit varying degrees of severity and rates of progression of HAD. Neuropathologic variables that are associated with the rate of progression of HAD are no...

Journal: :The Journal of Experimental Medicine 1993
B F Haynes L O Arthur P Frost T J Matthews A J Langlois T J Palker M K Hart R M Scearce D M Jones C McDanal

The fusogenic (F) domain of human immunodeficiency virus (HIV) gp41 envelope (env) protein has sequence similarities to many virus and mediates the fusion of HIV-infected cells. During a survey of the immunogenicity of HIV env peptides in chimpanzees, we have observed that HIV peptide immunogenicity was dramatically altered by the NH2-terminal synthesis of the gp41 F domain to an otherwise immu...

2014
John M. Louis Annie Aniana Katheryn Lohith Jane M. Sayer Julien Roche Carole A. Bewley G. Marius Clore

We previously reported a series of antibodies, in fragment antigen binding domain (Fab) formats, selected from a human non-immune phage library, directed against the internal trimeric coiled-coil of the N-heptad repeat (N-HR) of HIV-1 gp41. Broadly neutralizing antibodies from that series bind to both the fully exposed N-HR trimer, representing the pre-hairpin intermediate state of gp41, and to...

2017
Constantinos Kurt Wibmer Jason Gorman Gabriel Ozorowski Jinal N Bhiman Daniel J Sheward Debra H Elliott Julie Rouelle Ashley Smira M Gordon Joyce Nonkululeko Ndabambi Aliaksandr Druz Mangai Asokan Dennis R Burton Mark Connors Salim S Abdool Karim John R Mascola James E Robinson Andrew B Ward Carolyn Williamson Peter D Kwong Lynn Morris Penny L Moore

A comprehensive understanding of the regions on HIV-1 envelope trimers targeted by broadly neutralizing antibodies may contribute to rational design of an HIV-1 vaccine. We previously identified a participant in the CAPRISA cohort, CAP248, who developed trimer-specific antibodies capable of neutralizing 60% of heterologous viruses at three years post-infection. Here, we report the isolation by ...

Journal: :Journal of virology 2000
P N Nyambi H A Mbah S Burda C Williams M K Gorny A Nádas S Zolla-Pazner

We have examined the exposure and conservation of antigenic epitopes on the surface envelope glycoproteins (gp120 and gp41) of 26 intact, native, primary human immunodeficiency virus type 1 (HIV-1) group M virions of clades A to H. For this, 47 monoclonal antibodies (MAbs) derived from HIV-1-infected patients were used which were directed at epitopes of gp120 (specifically V2, C2, V3, the CD4-b...

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