Please use this identifier to cite or link to this item: http://buratest.brunel.ac.uk/handle/2438/13512
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dc.contributor.authorPednekar, L-
dc.contributor.authorPathan, AA-
dc.contributor.authorPaudyal, B-
dc.contributor.authorTsolaki, A-
dc.contributor.authorKaur, A-
dc.contributor.authorAbozaid, S-
dc.contributor.authorKouser, L-
dc.contributor.authorKhan, HA-
dc.contributor.authorPeerschke, EI-
dc.contributor.authorShamji, MH-
dc.contributor.authorStenbeck, G-
dc.contributor.authorGhebrehiwet, B-
dc.contributor.authorKishore, U-
dc.date.accessioned2016-11-17T15:13:19Z-
dc.date.available2016-11-17T15:13:19Z-
dc.date.issued2016-
dc.identifier.citationFrontiers in Immunology, 2016en_US
dc.identifier.issn1664-3224-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/13512-
dc.descriptionThis Document is Protected by copyright and was first published by Frontiers. All rights reserved. it is reproduced with permission.-
dc.description.abstracthe heterotrimeric globular head (gC1q) domain of human C1q is made up of the C-terminal ends of the three individual chains, ghA, ghB and ghC. The receptor for the gC1q domain is a multi-functional pattern recognition protein, gC1qR. Since understanding of gC1qR and gC1q interaction could provide an insight into the pleiotropic functions of gC1qR, this study was undertaken to identify the gC1qR binding site on the gC1q domain, using the recombinant ghA, ghB and ghC modules and their substitution mutants. Our results show that ghA, ghB and ghC modules can interact with gC1qR independently, thus reinforcing the notion of modularity within the gC1q domain of human C1q. Mutational analysis revealed that while Arg162 in the ghA module is central to interaction between gC1qR and C1q, a single amino acid substitution (Arginine to Glutamate) in residue 114 of the ghB module resulted in enhanced binding. Expression of gC1qR and C1q in adherent monocytes with or without pro-inflammatory stimuli was also analyzed by qPCR; it showed an autocrine/paracrine basis of C1q and gC1qR interaction. Microscopic studies revealed that C1q and gC1qR are co-localized on PBMCs. Cell proliferation assays indicated that ghA, ghB and ghC modules were able to attenuate PHA stimulated proliferation of PBMCs. Addition of gC1qR had an additive effect on the anti-proliferative effect of gh modules. In summary, our results identify residues involved in C1q interaction and explain, to a certain level, their involvement on the immune cell surface, which is relevant for C1q-induced functions including inflammation, infection and immunity.en_US
dc.language.isoenen_US
dc.subjectC1qen_US
dc.subjectGlobular headen_US
dc.subjectgC1qRen_US
dc.subjectProtein-protein interactionen_US
dc.subjectCell proliferationen_US
dc.titleAnalysis of the interaction between globular head modules of candidate receptor gC1qRen_US
dc.typeArticleen_US
dc.relation.isPartOfFrontiers in Immunology-
pubs.publication-statusAccepted-
Appears in Collections:Dept of Life Sciences Research Papers

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