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A Linear Epitope in the N-Terminal Domain of CCR5 and Its Interaction with Antibody

Chain, B; Arnold, J; Akthar, S; Brandt, M; Davis, D; Noursadeghi, M; Lapp, T; ... Chayen, N; + view all (2015) A Linear Epitope in the N-Terminal Domain of CCR5 and Its Interaction with Antibody. PLoS One , 10 (6) , Article e0128381. 10.1371/journal.pone.0128381. Green open access

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Abstract

The CCR5 receptor plays a role in several key physiological and pathological processes and is an important therapeutic target. Inhibition of the CCR5 axis by passive or active immunisation offers one very selective strategy for intervention. In this study we define a new linear epitope within the extracellular domain of CCR5 recognised by two independently produced monoclonal antibodies. A short peptide encoding the linear epitope can induce antibodies which recognise the intact receptor when administered colinear with a tetanus toxoid helper T cell epitope. The monoclonal antibody RoAb 13 is shown to bind to both cells and peptide with moderate to high affinity (6x10^8 and 1.2x107 M-1 respectively), and binding to the peptide is enhanced by sulfation of tyrosines at positions 10 and 14. RoAb13, which has previously been shown to block HIV infection, also blocks migration of monocytes in response to CCR5 binding chemokines and to inflammatory macrophage conditioned medium. A Fab fragment of RoAb13 has been crystallised and a structure of the antibody is reported to 2.1 angstrom resolution.

Type: Article
Title: A Linear Epitope in the N-Terminal Domain of CCR5 and Its Interaction with Antibody
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1371/journal.pone.0128381
Publisher version: http://dx.doi.org/10.1371/journal.pone.0128381
Language: English
Additional information: © 2015 Chain et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Infection and Immunity
URI: https://discovery.ucl.ac.uk/id/eprint/1472163
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