Analysis of the Native Quaternary Structure of Vanilloid Receptor 1* 210

Vanilloid receptor subtype 1 (VR1) is a ligand-gated channel that can be activated by capsaicin and other vanilloids as well as by protons and heat. In the present study, we have analyzed the oligomeric state of VR1. Co-immunoprecipitation of differently tagged VR1 molecules indicated that VR1 can form oligomers. Using two different heterologous VR1 expression systems as well as endogenous VR1 expressed in dorsal root ganglion cells, we analyzed oligomer formation using perfluoro-octanoic acid polyacrylamide gel electrophoresis. Results were confirmed both with chemical cross-linking agents as well as through endogenous cross-linking mediated by transglutaminase. Our results clearly show that VR1 forms multimers in each of the expression systems with a homotetramer as a predominant form. The oligomeric structure of VR1 may contribute to the complexity of VR1 pharmacology. Finally, differences in glycosylation between the systems were observed, indicating the need for caution in the use of the heterologous expression systems for analysis of VR1 properties.

[1]  W. Catterall,et al.  Structure and function of voltage-sensitive ion channels. , 1988, Science.

[2]  P. Blumberg,et al.  Differential Activation and Desensitization of Sensory Neurons by Resiniferatoxin , 1997, The Journal of Neuroscience.

[3]  R. Rice,et al.  Transglutaminases: multifunctional cross‐linking enzymes that stabilize tissues , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[4]  S. Yuspa,et al.  Protein kinase C regulates keratinocyte transglutaminase (TGK) gene expression in cultured primary mouse epidermal keratinocytes induced to terminally differentiate by calcium. , 1994, The Journal of investigative dermatology.

[5]  D. Julius,et al.  The capsaicin receptor: a heat-activated ion channel in the pain pathway , 1997, Nature.

[6]  M. Imai,et al.  Cloning of a Stretch-inhibitable Nonselective Cation Channel* , 1999, The Journal of Biological Chemistry.

[7]  L. Fésüs,et al.  Searching for the function of tissue transglutaminase: its possible involvement in the biochemical pathway of programmed cell death. , 1988, Advances in experimental medicine and biology.

[8]  P. Blumberg,et al.  Vanilloid receptors: new insights enhance potential as a therapeutic target , 1996, Pain.

[9]  M. Schumacher,et al.  Molecular Cloning of an N-terminal Splice Variant of the Capsaicin Receptor , 2000, The Journal of Biological Chemistry.

[10]  D. Kim,et al.  Capsaicin activates a nonselective cation channel in cultured neonatal rat dorsal root ganglion neurons , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  M. Hingorani,et al.  Oligomeric structure of bacteriophage T7 DNA primase/helicase proteins. , 1993, The Journal of biological chemistry.

[12]  Makoto Tominaga,et al.  Acid potentiation of the capsaicin receptor determined by a key extracellular site , 2000 .

[13]  S. Deschamps,et al.  Oligomerization State of Water Channels and Glycerol Facilitators , 1998, The Journal of Biological Chemistry.

[14]  O. Kretz,et al.  TRP4 (CCE1) Protein Is Part of Native Calcium Release-activated Ca2+-like Channels in Adrenal Cells* , 2000, The Journal of Biological Chemistry.

[15]  D. Clapham,et al.  Number and Stoichiometry of Subunits in the Native Atrial G-protein-gated K+ Channel, IKACh * , 1998, The Journal of Biological Chemistry.

[16]  R. MacKinnon Determination of the subunit stoichiometry of a voltage-activated potassium channel , 1991, Nature.

[17]  Brij B. Singh,et al.  Assembly of Trp1 in a Signaling Complex Associated with Caveolin-Scaffolding Lipid Raft Domains* , 2000, The Journal of Biological Chemistry.

[18]  R. Elde,et al.  Immunocytochemical localization of the vanilloid receptor 1 (VR1): relationship to neuropeptides, the P2X3 purinoceptor and IB4 binding sites , 1999, The European journal of neuroscience.

[19]  P. Blumberg,et al.  Molecular target size of the vanilloid (capsaicin) receptor in pig dorsal root ganglia. , 1991, Life sciences.

[20]  C. Romanin,et al.  Coassembly of Trp1 and Trp3 proteins generates diacylglycerol- and Ca2+-sensitive cation channels. , 2000 .

[21]  A. Jancsó-Gábor,et al.  Sensory effects of capsaicin congeners I. Relationship between chemical structure and pain-producing potency of pungent agents. , 1975, Arzneimittel-Forschung.

[22]  P. Blumberg,et al.  The cloned rat vanilloid receptor VR1 mediates both R-type binding and C-type calcium response in dorsal root ganglion neurons. , 1999, Molecular pharmacology.

[23]  G. Schultz,et al.  From worm to man: three subfamilies of TRP channels , 2000, Trends in Neurosciences.

[24]  C. Montell,et al.  Coordination of an Array of Signaling Proteins through Homo- and Heteromeric Interactions Between PDZ Domains and Target Proteins , 1998, The Journal of cell biology.

[25]  D. Julius,et al.  A capsaicin-receptor homologue with a high threshold for noxious heat , 1999, Nature.

[26]  A I Basbaum,et al.  Impaired nociception and pain sensation in mice lacking the capsaicin receptor. , 2000, Science.

[27]  C. Montell,et al.  Coassembly of TRP and TRPL Produces a Distinct Store-Operated Conductance , 1997, Cell.

[28]  T. Jessell PAIN , 1982, The Lancet.

[29]  R. Prinjha,et al.  Characterization using FLIPR of rat vanilloid receptor (rVR1) pharmacology , 2000, British journal of pharmacology.

[30]  S. Bevan,et al.  Sensory neuron-specific actions of capsaicin: mechanisms and applications. , 1990, Trends in pharmacological sciences.

[31]  C. Goso,et al.  Characterization of a peripheral vanilloid (capsaicin) receptor in the urinary bladder of the rat. , 1993, Life sciences.

[32]  E. De Clercq,et al.  Chemical crosslinking of the subunits of HIV‐1 reverse transcriptase , 1996, Protein science : a publication of the Protein Society.

[33]  D. Wilkin,et al.  Neuron , 2001, Brain Research.

[34]  A. Basbaum,et al.  The Cloned Capsaicin Receptor Integrates Multiple Pain-Producing Stimuli , 1998, Neuron.

[35]  L. Huan,et al.  Novel method for evaluation of the oligomeric structure of membrane proteins. , 1999 .

[36]  M. Paulsson,et al.  Expression of tissue transglutaminase in skeletal tissues correlates with events of terminal differentiation of chondrocytes , 1993, The Journal of cell biology.

[37]  L. Fésüs Biochemical events in naturally occurring forms of cell death. , 1993 .

[38]  R. Reithmeier,et al.  Self-association of Band 3, the human erythrocyte anion exchanger, in detergent solution. , 1997, Biochimica et biophysica acta.

[39]  M. Iadarola,et al.  Ligand-induced Dynamic Membrane Changes and Cell Deletion Conferred by Vanilloid Receptor 1* , 2001, The Journal of Biological Chemistry.

[40]  H. Handwerker,et al.  Selective excitation by capsaicin of mechano-heat sensitive nociceptors in rat skin , 1988, Brain Research.

[41]  Peter M. Blumberg,et al.  Specific binding of resiniferatoxin, an ultrapotent capsaicin analog, by dorsal root anglion membranes , 1990, Brain Research.

[42]  S. Bingham,et al.  Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia , 2000, Nature.

[43]  M. Saraste,et al.  FEBS Lett , 2000 .