Allosterism in human complement component 5a (hC5a): A damper of C5a receptor (C5aR) signaling

Abstract

The phenomena of allosterism continues to advance the field of drug discovery, by illuminating gainful insights for many key processes, related to the structure-function relationships in proteins and enzymes, including the transmembrane G-protein coupled receptors (GPCRs), both in normal as well as in the disease states. However, allosterism is completely unexplored in the native protein ligands, especially when a small covalent change significantly modulates the pharmacology of the protein ligands toward the signaling axes of the GPCRs. One such example is the human C5a (hC5a), the potent cationic anaphylatoxin that engages C5aR and C5L2 to elicit numerous immunological and non-immunological responses in humans. From the recently available structure-function data, it is clear that unlike the mouse C5a (mC5a), thehC5a displays conformational heterogeneity. However, the molecular basis of such conformational heterogeneity, otherwise allosterism inhC5a and its precise contribution toward the overall C5aR signaling is not known. This study attempts to decipher the functional role of allosterism inhC5a, by exploring the inherent conformational dynamics inmC5a,hC5a and in its point mutants, including the proteolytic mutant des-Arg74_hC5a. Prima facie, the comparative molecular dynamics study, over total 500 ns, identifies Arg74_Tyr23 and Arg37_Phe51 �cation-?� pairs as the molecular �allosteric switches� onhC5a that potentially functions as a damper of C5aR signaling. � 2015 Taylor & Francis.