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Dr Mark Young 


Introduction

P2X receptors are ATP-gated ion channels which play key roles in a variety of physiological processes such as synaptic transmission, taste sensation and smooth muscle control.  They function in cells as trimers, with two transmembrane domains per monomer and large, glycosylated extracellular domains.

P2X receptors are important drug targets primarily because of their involvement in pain following nerve damage and inflammation.  In a rat model of neuropathic pain, tactile allodynia was abolished when levels of the P2X4 receptor subtype were knocked down using antisense oligonucleotides [1].  It is therefore likely that drugs which target P2X4 may have significant analgesic properties, but the current lack of human P2X4-selective antagonists is hampering research into its specific roles.

Our understanding of the structure of human P2X4 is limited to 21Å resolution at present [2], but the recent publication of the 3D crystal structures of a truncated mutant of zebrafish P2X4.1 in both the closed and ATP-bound open state [3] raises hopes that crystal structures of suitably modified human P2X receptors can be determined. High-resolution structures of the ligand-binding sites of human P2X receptors, solved in the presence of ATP, would enable structure-based drug design, leading to new analgesic and anti-inflammatory therapies.

P2X receptors are also involved in inflammation. The P2X7 receptor subtype is expressed in immune cells; and in knock-out mice lacking P2X7, chronic inflammatory pain was abolished, while acute pain responses remained unchanged [4]. P2X7 is unique among the P2X receptors in that its activation leads to the release of pro-inflammatory cytokines, and prolonged activation causes cell death [5]. The properties of P2X7 are regulated by its long intracellular C-terminal domain, which couples ion channel activation to downstream signalling, and it has recently been suggested that targeting P2X7-mediated downstream signalling might represent a good strategy to develop more selective anti-inflammatory drugs [6].

Aims

Optimisation of human P2X4 for 3D-structure determination

Previously, His-tagged human P2X4 trimers (over-expressed in human cells) were purified by a combination of metal affinity chromatography and non-denaturing gel electrophoresis.  Electron microscopy of single protein particles was used to determine a 3D structure at a resolution of 21Å [2].  The dimensions and overall architecture of the low-resolution structure were highly consistent with that of the 3D crystal structure of the closed state of zebrafish P2X4.1 [7], and the fit of the extracellular domain was particularly good (Figure 1).

Using large-scale mammalian cell culture at the Oxford Protein Production Facility (collaboration with Dr Ray Owens), we can recover ~1 mg of human P2X4 protein from one 50-bottle roller culture run (~6x109 cells), which is sufficient for structural studies using both 2D and 3D crystallography.  We are currently exploring ways to optimise human P2X4 constructs for structural study using a combination of mutagenesis, biochemical analysis and functional assay.

Exploring the expression of P2X receptors in other eukaryotic systems

We have also expressed P2X receptors in both baculovirus-infected insect cells [8] collaboration with Dr Mark Parker, Case Western, USA) and the yeast Saccharomyces cerevisiae.  Insect cell expression was successfully used in solving the structure of zebrafish P2X4.1 [7], so it represents a proven system for the expression of P2X receptors.  We are currently developing the fruit fly Drosophila melanogaster as an expression system for membrane proteins (collaboration with Dr Wynand Van der Goes Van Naters).

 

P2X receptors

The yeast system has the advantages of being both cost-effective and easy to use; initial expression trials of rat P2X7 are encouraging and, once suitably optimised, this system will provide a straightforward way to screen multiple constructs for expression, folding and suitability for further structural studies.

P2X7 downstream signalling pathways

Upon activation by extracellular ATP, P2X7 couples via its long C-terminal domain to several intracellular signalling pathways, leading to recruitment of the NRLP3 inflammasome and release of pro-inflammatory cytokines [5]. This signalling has important consequences in pain and inflammation, particularly in conditions of chronic inflammation such as arthritis and Alzheimer’s disease. Although many downstream components of the signalling pathways have been characterised, the molecular basis of the first step in this process remains unknown. What is the 3D-structure of the P2X7 C-terminal domain, which proteins does it interact with, and how are these interactions regulated? In collaboration with Dr Amanda MacKenzie (University of Bath), we are currently using the isolated, purified P2X7 C-terminal domain in structural and proteomic studies to address these questions.

Tsuda M et al. (2003) P2X4 receptors induced in spinal microglia gate tactile allodynia after nerve injury. Nature 424, 778-783

Young MT et al. (2008) Molecular shape, architecture, and size of P2X4 receptors determined using fluorescence resonance energy transfer and electron microscopy. J Biol Chem 283, 26241-26251

Hattori M and Gouaux E (2012) Molecular mechanism of ATP binding and ion channel activation in P2X receptors. Nature 485, 207-212

Chessell IP et al. (2005) Disruption of the P2X7 purinoceptor gene abolishes chronic inflammatory and neuropathic pain. Pain 114, 386-396

Surprenant A and North RA (2009) Signaling at purinergic P2X receptors. Annu Rev Physiol 71, 333-359

Sorge RE et al. (2012) Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity. Nat Med 18, 595-599

Kawate T et al. (2009) Crystal structure of the ATP-gated P2X4 ion channel in the closed state. Nature 460, 592-598

Valente M et al. (2011) Expression, purification, electron microscopy, N-glycosylation mutagenesis and molecular modelling of human P2X4 and Dictyostelium discoideum P2XA. Biochim Biophys Acta 1808, 2859-2866

Collaborators

Cardiff University

Dr Pierre Rizkallah

Professor Kenneth Harris

Oxford Protein Production Facility:    

Dr Ray Owens

Case Western (USA):                              

Dr Mark Parker

University of Bath                                  

Dr Amanda MacKenzie