The Role of Antibody Polyspecificity and Lipid Reactivity in Binding of Broadly Neutralizing Anti-HIV-1 Envelope Human Monoclonal Antibodies 2F5 and 4E10 to Glycoprotein 41 Membrane Proximal Envelope Epitopes Export

@article{citeulike:2766839, abstract = {Two neutralizing human mAbs, 2F5 and 4E10, that react with the HIV-1 envelope gp41 membrane proximal region are also polyspecific autoantibodies that bind to anionic phospholipids. To determine the autoantibody nature of these Abs, we have compared their reactivities with human anti-cardiolipin mAbs derived from a primary antiphospholipid syndrome patient. To define the role of lipid polyreactivity in binding of 2F5 and 4E10 mAbs to HIV-1 envelope membrane proximal epitopes, we determined the kinetics of binding of mAbs 2F5 and 4E10 to their nominal gp41 epitopes vs liposome-gp41 peptide conjugates. Both anti-HIV-1 mAbs 2F5 and 4E10 bound to cardiolipin with Kd values similar to those of autoimmune anti-cardiolipin Abs, IS4 and IS6. Binding kinetics studies revealed that mAb 2F5 and 4E10 binding to their respective gp41 peptide-lipid conjugates could best be defined by a two-step (encounter-docking) conformational change model. In contrast, binding of 2F5 and 4E10 mAbs to linear peptide epitopes followed a simple Langmuir model. A mouse mAb, 13H11, that cross-blocks mAb 2F5 binding to the gp41 epitope did not cross-react with lipids nor did it neutralize HIV-1 viruses. Taken together, these data demonstrate the similarity of 2F5 and 4E10 mAbs to known anti-cardiolipin Abs and support the model that mAb 2F5 and 4E10 binding to HIV-1 involves both viral lipid membrane and gp41 membrane proximal epitopes.}, author = {Alam, Munir S. and Mcadams, Mildred and Boren, David and Rak, Michael and Scearce, Richard M. and Gao, Feng and Camacho, Zenaido T. and Gewirth, Daniel and Kelsoe, Garnett and Chen, Pojen and Haynes, Barton F.}, citeulike-article-id = {2766839}, citeulike-linkout-0 = {http://www.jimmunol.org/cgi/content/abstract/178/7/4424}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/17372000}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=17372000}, day = {1}, journal = {J Immunol}, keywords = {2f5, 4e10, neutralization}, month = {April}, number = {7}, pages = {4424--4435}, posted-at = {2008-05-07 16:39:37}, priority = {2}, title = {The Role of Antibody Polyspecificity and Lipid Reactivity in Binding of Broadly Neutralizing Anti-HIV-1 Envelope Human Monoclonal Antibodies 2F5 and 4E10 to Glycoprotein 41 Membrane Proximal Envelope Epitopes}, url = {http://www.jimmunol.org/cgi/content/abstract/178/7/4424}, volume = {178}, year = {2007} }

TY - JOUR ID - citeulike:2766839 L3 - citeulike-article-id:2766839 N2 - Two neutralizing human mAbs, 2F5 and 4E10, that react with the HIV-1 envelope gp41 membrane proximal region are also polyspecific autoantibodies that bind to anionic phospholipids. To determine the autoantibody nature of these Abs, we have compared their reactivities with human anti-cardiolipin mAbs derived from a primary antiphospholipid syndrome patient. To define the role of lipid polyreactivity in binding of 2F5 and 4E10 mAbs to HIV-1 envelope membrane proximal epitopes, we determined the kinetics of binding of mAbs 2F5 and 4E10 to their nominal gp41 epitopes vs liposome-gp41 peptide conjugates. Both anti-HIV-1 mAbs 2F5 and 4E10 bound to cardiolipin with Kd values similar to those of autoimmune anti-cardiolipin Abs, IS4 and IS6. Binding kinetics studies revealed that mAb 2F5 and 4E10 binding to their respective gp41 peptide-lipid conjugates could best be defined by a two-step (encounter-docking) conformational change model. In contrast, binding of 2F5 and 4E10 mAbs to linear peptide epitopes followed a simple Langmuir model. A mouse mAb, 13H11, that cross-blocks mAb 2F5 binding to the gp41 epitope did not cross-react with lipids nor did it neutralize HIV-1 viruses. Taken together, these data demonstrate the similarity of 2F5 and 4E10 mAbs to known anti-cardiolipin Abs and support the model that mAb 2F5 and 4E10 binding to HIV-1 involves both viral lipid membrane and gp41 membrane proximal epitopes. IS - 7 JF - J Immunol EP - 4435 TI - The Role of Antibody Polyspecificity and Lipid Reactivity in Binding of Broadly Neutralizing Anti-HIV-1 Envelope Human Monoclonal Antibodies 2F5 and 4E10 to Glycoprotein 41 Membrane Proximal Envelope Epitopes VL - 178 SP - 4424 KW - 2f5 KW - 4e10 KW - neutralization AU - Alam, Munir AU - Mcadams, Mildred AU - Boren, David AU - Rak, Michael AU - Scearce, Richard AU - Gao, Feng AU - Camacho, Zenaido AU - Gewirth, Daniel AU - Kelsoe, Garnett AU - Chen, Pojen AU - Haynes, Barton PY - 2007/04/01/ UR - http://www.jimmunol.org/cgi/content/abstract/178/7/4424 ER -