Esmaielbeiki, Reyhaneh, Naughton, Declan and Nebel, Jean-Christophe (2012) Structure prediction of LDLR-HNP1 complex based on docking enhanced by LDLR binding 3D motif. Protein and Peptide Letters, 19(4), pp. 458-467. ISSN (print) 0929-8665Full text not available from this archive.
Human antimicrobial peptides (AMPs), including defensins, have come under intense scrutiny owing to their key multiple roles as antimicrobial agents. Not only do they display direct action on microbes, but also recently they have shown to interact with the immune system to increase antimicrobial activity. Unfortunately, since mechanisms involved in the binding of AMPs to mammalian cells are largely unknown, their potential as novel anti-infective agents cannot be exploited yet. Following the reported interaction of Human Neutrophil Peptide 1 dimer (HNP1) with a low density lipoprotein receptor (LDLR), a computational study was conducted to discover their putative mode of interaction. State-of-the-art docking software produced a set of LDLR-HNP1 complex 3D models. Creation of a 3D motif capturing atomic interactions of LDLR binding interface allowed selection of the most plausible configurations. Eventually, only two models were in agreement with the literature. Binding energy estimations revealed that not only one of them is particularly stable, but also interaction with LDLR weakens significantly bonds within the HNP1 dimer. This may be significant since it suggests a mechanism for internalisation of HNP1 in mammalian cells. In addition to a novel approach for complex structure prediction, this study proposes a 3D model of the LDLR-HNP1 complex which highlights the key residues which are involved in the interactions. The putative identification of the receptor binding mechanism should inform the future design of synthetic HNPs to afford maximum internalisation, which could lead to novel anti-infective drugs.
|Uncontrolled Keywords:||low density lipoprotein receptor, 3d motif, protein-protein interaction, docking, human alpha defensin, human immune system, low-density-lipoprotein, ligand recognition, protein complexes, rap complex, rounds 6-11, in-vitro, receptor, generation, cluspro, capri|
|Research Area:||Allied health professions and studies
|Faculty, School or Research Centre:||Faculty of Science, Engineering and Computing
Faculty of Science, Engineering and Computing > School of Life Sciences
|Depositing User:||Automatic Import Agent|
|Date Deposited:||03 Jan 2012 15:54|
|Last Modified:||17 Jan 2013 14:04|
Actions (Repository Editors)
|Item Control Page|