Source:http://linkedlifedata.com/resource/pubmed/id/20164234
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003250,
umls-concept:C0012655,
umls-concept:C0017982,
umls-concept:C0019691,
umls-concept:C0019704,
umls-concept:C0086418,
umls-concept:C0205145,
umls-concept:C0205147,
umls-concept:C0205369,
umls-concept:C0521026,
umls-concept:C0851285,
umls-concept:C1167622,
umls-concept:C1332714,
umls-concept:C1422036,
umls-concept:C1446680,
umls-concept:C1514562,
umls-concept:C1880389,
umls-concept:C1883204,
umls-concept:C1883221
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pubmed:issue |
9
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pubmed:dateCreated |
2010-4-7
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pubmed:abstractText |
A recombinant human monoclonal antibody, IgG1 b12 (b12), recognizes a conformational epitope on human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein (Env) gp120 that overlaps the CD4 binding domain. Although b12 is able to broadly neutralize HIV-1 subtype B, C, and D viruses, many HIV-1 CRF01_AE viruses are resistant to b12-mediated neutralization. In this report, we examined the molecular mechanisms underlying the low neutralization susceptibility of CRF01_AE viruses to b12, using recently established CRF01_AE Env recombinant viruses. Our results showed that two potential N-linked glycosylation (PNLG) sites in the V2 and C2 regions of Env gp120 played an important role in regulating the susceptibility of CRF01_AE Env to b12. The locations of these PNLG sites correspond to amino acid positions 186 and 197 in HXB2 Env gp120; thus, they are designated N186 and N197 in this study. Removal of N186 significantly conferred the b12 susceptibility of 2 resistant CRF01_AE Env clones, 65CC4 and 107CC2, while the introduction of N186 reduced the b12 susceptibility of a susceptible CRF01_AE Env clone, 65CC1. In addition, removal of both N186 and N197 conferred the b12 susceptibility of 3 resistant CRF01_AE Env clones, 45PB1, 62PL1, and 101PL1, whereas the removal of either N186 or N197 was not sufficient to confer the b12 susceptibility of these CRF01_AE Env clones. Finally, removal of N197 conferred the b12 susceptibility of 2 resistant CRF01_AE Env clones lacking N186, 55PL1 and 102CC2. Taken together, we propose that two PNLG sites, N186 and N197, in Env gp120 are important determinants of the b12 resistance of CRF01_AE viruses.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Neutralizing,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Envelope Protein gp120,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Mutant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/gp120 protein, Human...
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1098-5514
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
84
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4311-20
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pubmed:dateRevised |
2010-11-2
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pubmed:meshHeading |
pubmed-meshheading:20164234-Amino Acid Sequence,
pubmed-meshheading:20164234-Antibodies, Monoclonal,
pubmed-meshheading:20164234-Antibodies, Neutralizing,
pubmed-meshheading:20164234-Binding Sites,
pubmed-meshheading:20164234-Epitopes,
pubmed-meshheading:20164234-Glycosylation,
pubmed-meshheading:20164234-HIV Antibodies,
pubmed-meshheading:20164234-HIV Envelope Protein gp120,
pubmed-meshheading:20164234-HIV-1,
pubmed-meshheading:20164234-Humans,
pubmed-meshheading:20164234-Immunoglobulin G,
pubmed-meshheading:20164234-Molecular Sequence Data,
pubmed-meshheading:20164234-Mutant Proteins,
pubmed-meshheading:20164234-Neutralization Tests,
pubmed-meshheading:20164234-Protein Processing, Post-Translational
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pubmed:year |
2010
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pubmed:articleTitle |
Two N-linked glycosylation sites in the V2 and C2 regions of human immunodeficiency virus type 1 CRF01_AE envelope glycoprotein gp120 regulate viral neutralization susceptibility to the human monoclonal antibody specific for the CD4 binding domain.
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pubmed:affiliation |
Thailand-Japan Research Collaboration Center on Emerging and Re-emerging Infections (RCC-ERI), Nonthaburi 11000, Thailand.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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