Conformational Preferences of a Chimeric Peptide HIV-1 Immunogen from the C4−V3 Domains of gp120 Envelope Protein of HIV-1 CAN0A Based on Solution NMR:  Comparison to a Related Immunogenic Peptide from HIV-1 RF†

Biochemistry ◽  
1996 ◽  
Vol 35 (16) ◽  
pp. 5158-5165 ◽  
Author(s):  
Hai M. Vu ◽  
Robert de Lorimier ◽  
M. Anthony Moody ◽  
Barton F. Haynes ◽  
Leonard D. Spicer
Keyword(s):  
Envelope Protein ◽  
Solution Nmr ◽  
Immunogenic Peptide ◽  
Chimeric Peptide ◽  
Gp120 Envelope ◽  
Conformational Preferences ◽  
Hiv 1

scholarly journals P12-11. Resistance to the CD4 mimetic mini protein M48-U1 induces changes in a highly conserved region on the HIV-1 gp120 envelope protein

Retrovirology ◽  
2009 ◽  
Vol 6 (S3) ◽  
Author(s):  
K Grupping ◽  
L Heyndrickx ◽  
J Michiels ◽  
G Martin ◽  
L Martin ◽  
...  
Keyword(s):  
Envelope Protein ◽  
Gp120 Envelope ◽  
Conserved Region ◽  
Hiv 1

scholarly journals Sequence-Conserved and Antibody-Accessible Sites in the V1V2 Domain of HIV-1 gp120 Envelope Protein

2014 ◽  
Vol 30 (9) ◽  
pp. 927-931 ◽  
Author(s):  
Evgeny Shmelkov ◽  
Arsen Grigoryan ◽  
Chavdar Krachmarov ◽  
Ruben Abagyan ◽  
Timothy Cardozo
Keyword(s):  
Envelope Protein ◽  
Gp120 Envelope ◽  
Hiv 1

Jacalin, a lectin with anti-HIV-1 properties, and HIV-1 gp120 envelope protein interact with distinct regions of the CD4 molecule

1994 ◽  
Vol 31 (8) ◽  
pp. 569-575 ◽  
Author(s):  
Pierre Corbeau ◽  
Muriel Haran ◽  
Hans Binz ◽  
Christian Devaux
Keyword(s):  
Envelope Protein ◽  
Gp120 Envelope ◽  
Anti Hiv ◽  
Hiv 1

Different HIV-1 gp120 envelope protein mutants differentially affect calcium responses in cultured cortical astrocytes

2005 ◽  
Vol 32 (S 4) ◽  
Author(s):  
R Steinbach ◽  
H Schaal ◽  
T Nolting ◽  
M Schreiber ◽  
G Arendt ◽  
...  
Keyword(s):  
Envelope Protein ◽  
Gp120 Envelope ◽  
Cortical Astrocytes ◽  
Protein Mutants ◽  
Hiv 1

scholarly journals Human immunodeficiency virus type 1 gp120 envelope characteristics associated with disease progression differ in family members infected with genetically similar viruses

2013 ◽  
Vol 94 (1) ◽  
pp. 20-29 ◽  
Author(s):  
Elly Baan ◽  
Renée M. van der Sluis ◽  
Margreet E. Bakker ◽  
Vincent Bekker ◽  
Dasja Pajkrt ◽  
...  
Keyword(s):  
Human Immunodeficiency Virus ◽  
Disease Progression ◽  
Human Immunodeficiency Virus Type ◽  
Virus Type ◽  
Positive Charge ◽  
Gp120 Envelope ◽  
Immunodeficiency Virus ◽  
Virus Strains ◽  
Hiv 1

The human immunodeficiency virus type 1 (HIV-1) envelope protein provides the primary contact between the virus and host, and is the main target of the adaptive humoral immune response. The length of gp120 variable loops and the number of N-linked glycosylation events are key determinants for virus infectivity and immune escape, while the V3 loop overall positive charge is known to affect co-receptor tropism. We selected two families in which both parents and two children had been infected with HIV-1 for nearly 10 years, but who demonstrated variable parameters of disease progression. We analysed the gp120 envelope sequence and compared individuals that progressed to those that did not in order to decipher evolutionary alterations that are associated with disease progression when individuals are infected with genetically related virus strains. The analysis of the V3-positive charge demonstrated an association between higher V3-positive charges with disease progression. The ratio between the amino acid length and the number of potential N-linked glycosylation sites was also shown to be associated with disease progression with the healthier family members having a lower ratio. In conclusion in individuals initially infected with genetically linked virus strains the V3-positive charges and N-linked glycosylation are associated with HIV-1 disease progression and follow varied evolutionary paths for individuals with varied disease progression.

scholarly journals A glycoside analog of mammalian oligomannose formulated with a TLR4-stimulating adjuvant elicits HIV-1 cross-reactive antibodies

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jean-François Bruxelle ◽  
Tess Kirilenko ◽  
Nino Trattnig ◽  
Yiqiu Yang ◽  
Matteo Cattin ◽  
...  
Keyword(s):  
Transgenic Mice ◽  
Envelope Protein ◽  
Protein Sequence ◽  
Neutralizing Antibodies ◽  
Human Antibody ◽  
Broadly Neutralizing Antibodies ◽  
Specific Antibodies ◽  
Strong Binding ◽  
Hiv Envelope ◽  
Hiv 1

AbstractThe occurrence of oligomannose-specific broadly neutralizing antibodies (bnAbs) has spurred efforts to develop immunogens that can elicit similar antibodies. Here, we report on the antigenicity and immunogenicity of a CRM197-conjugate of a previously reported oligomannose mimetic. Oligomannose-specific bnAbs that are less dependent on interactions with the HIV envelope protein sequence showed strong binding to the glycoconjugates, with affinities approximating those reported for their cognate epitope. The glycoconjugate is also recognized by inferred germline precursors of oligomannose-specific bnAbs, albeit with the expected low avidity, supporting its potential as an immunogen. Immunization of human-antibody transgenic mice revealed that only a TLR4-stimulating adjuvant formulation resulted in antibodies able to bind a panel of recombinant HIV trimers. These antibodies bound at relatively modest levels, possibly explaining their inability to neutralize HIV infectivity. Nevertheless, these findings contribute further to understanding conditions for eliciting HIV-cross-reactive oligomannose-specific antibodies and inform on next steps for improving on the elicited response.

scholarly journals Antibody responses to prime–boost vaccination with an HIV-1 gp145 envelope protein and chimpanzee adenovirus vectors expressing HIV-1 gp140

AIDS ◽  
2016 ◽  
Vol 30 (16) ◽  
pp. 2405-2414 ◽  
Author(s):  
Kristel L. Emmer ◽  
Lindsay Wieczorek ◽  
Steven Tuyishime ◽  
Sebastian Molnar ◽  
Victoria R. Polonis ◽  
...  
Keyword(s):  
Envelope Protein ◽  
Antibody Responses ◽  
Boost Vaccination ◽  
Adenovirus Vectors ◽  
Hiv 1
Sign in / Sign up

Export Citation Format

Share Document