Please use this identifier to cite or link to this item: http://buratest.brunel.ac.uk/handle/2438/13512
Title: Analysis of the interaction between globular head modules of candidate receptor gC1qR
Authors: Pednekar, L
Pathan, AA
Paudyal, B
Tsolaki, A
Kaur, A
Abozaid, S
Kouser, L
Khan, HA
Peerschke, EI
Shamji, MH
Stenbeck, G
Ghebrehiwet, B
Kishore, U
Keywords: C1q;Globular head;gC1qR;Protein-protein interaction;Cell proliferation
Issue Date: 2016
Citation: Frontiers in Immunology, 2016
Abstract: he 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.
Description: This Document is Protected by copyright and was first published by Frontiers. All rights reserved. it is reproduced with permission.
URI: http://bura.brunel.ac.uk/handle/2438/13512
ISSN: 1664-3224
Appears in Collections:Dept of Life Sciences Research Papers

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