tyrosine-o-sulfate and Acquired-Immunodeficiency-Syndrome

tyrosine-o-sulfate has been researched along with Acquired-Immunodeficiency-Syndrome* in 1 studies

Other Studies

1 other study(ies) available for tyrosine-o-sulfate and Acquired-Immunodeficiency-Syndrome

Article	Year
Structural basis of tyrosine sulfation and VH-gene usage in antibodies that recognize the HIV type 1 coreceptor-binding site on gp120. Proceedings of the National Academy of Sciences of the United States of America, 2004, Mar-02, Volume: 101, Issue:9 The conserved surface of the HIV-1 gp120 envelope glycoprotein that binds to the HIV-1 coreceptor is protected from humoral recognition by multiple layers of camouflage. Here we present sequence and genomic analyses for 12 antibodies that pierce these defenses and determine the crystal structures of 5. The data reveal mechanisms and atomic-level details for three unusual immune features: posttranslational mimicry of coreceptor by tyrosine sulfation of antibody, an alternative molecular mechanism controlling such sulfation, and highly selective V(H)-gene usage. When confronted by extraordinary viral defenses, the immune system unveils novel adaptive capabilities, with tyrosine sulfation enhancing the vocabulary of antigen recognition. Topics: Acquired Immunodeficiency Syndrome; Amino Acid Sequence; Antibody Formation; CD4 Antigens; Crystallography, X-Ray; Genes, Immunoglobulin; HIV Envelope Protein gp120; HIV Infections; HIV-1; Humans; Immunoglobulin Fab Fragments; Immunoglobulin Heavy Chains; Immunoglobulin Joining Region; Immunoglobulin Variable Region; Molecular Sequence Data; Sulfates; Tyrosine	2004

Article

Year

Structural basis of tyrosine sulfation and VH-gene usage in antibodies that recognize the HIV type 1 coreceptor-binding site on gp120.

Proceedings of the National Academy of Sciences of the United States of America, 2004, Mar-02, Volume: 101, Issue:9

The conserved surface of the HIV-1 gp120 envelope glycoprotein that binds to the HIV-1 coreceptor is protected from humoral recognition by multiple layers of camouflage. Here we present sequence and genomic analyses for 12 antibodies that pierce these defenses and determine the crystal structures of 5. The data reveal mechanisms and atomic-level details for three unusual immune features: posttranslational mimicry of coreceptor by tyrosine sulfation of antibody, an alternative molecular mechanism controlling such sulfation, and highly selective V(H)-gene usage. When confronted by extraordinary viral defenses, the immune system unveils novel adaptive capabilities, with tyrosine sulfation enhancing the vocabulary of antigen recognition.

Topics: Acquired Immunodeficiency Syndrome; Amino Acid Sequence; Antibody Formation; CD4 Antigens; Crystallography, X-Ray; Genes, Immunoglobulin; HIV Envelope Protein gp120; HIV Infections; HIV-1; Humans; Immunoglobulin Fab Fragments; Immunoglobulin Heavy Chains; Immunoglobulin Joining Region; Immunoglobulin Variable Region; Molecular Sequence Data; Sulfates; Tyrosine

2004