A. Miyawaki and Y. Niino, Molecular Spies for Bioimaging???Fluorescent Protein-Based Probes, Molecular Cell, vol.58, issue.4, pp.632-643, 2015.
DOI : 10.1016/j.molcel.2015.03.002

M. A. Ayoub, Resonance Energy Transfer-Based Approaches to Study GPCRs, Methods Cell Biol, vol.132, pp.255-292, 2016.
DOI : 10.1016/bs.mcb.2015.10.008

URL : https://hal.archives-ouvertes.fr/hal-01353276

T. Niehörster, A. Löschberger, and M. Sauer, Multi-target spectrally resolved fluorescence lifetime imaging microscopy, Nature Methods, vol.81, issue.3, pp.257-262, 2016.
DOI : 10.1016/j.bpj.2008.10.068

H. E. Grecco, S. Imtiaz, and E. Zamir, Multiplexed imaging of intracellular protein networks, Cytometry Part A, vol.521, issue.8, pp.761-775, 2016.
DOI : 10.1038/nature14541

D. E. Clapham, TRP channels as cellular sensors, Nature, vol.36, issue.6966, pp.517-524, 2003.
DOI : 10.1016/S0896-6273(02)01048-6

Y. Kaneko and A. Szallasi, Transient receptor potential (TRP) channels: a clinical perspective, British Journal of Pharmacology, vol.400, issue.10, pp.2474-2507, 2014.
DOI : 10.1038/22761

L. Vay, C. Gu, and P. A. Mcnaughton, The thermo-TRP ion channel family: properties and therapeutic implications, British Journal of Pharmacology, vol.10, issue.4, pp.787-801, 2012.
DOI : 10.1038/nn1843

A. M. Loening, T. D. Fenn, and S. S. Gambhir, Consensus guided mutagenesis of Renilla luciferase yields enhanced stability and light output, Protein Engineering Design and Selection, vol.19, issue.9, pp.391-400, 2006.
DOI : 10.1093/protein/gzl023

M. Erard, A. Fredj, and F. Merola, Minimum set of mutations needed to optimize cyan fluorescent proteins for live cell imaging, Mol. BioSyst., vol.28, issue.2, pp.258-267, 2013.
DOI : 10.1021/bi00434a038

URL : https://hal.archives-ouvertes.fr/hal-01545402

Y. Percherancier, Y. A. Berchiche, and N. Heveker, Bioluminescence Resonance Energy Transfer Reveals Ligand-induced Conformational Changes in CXCR4 Homo- and Heterodimers, Journal of Biological Chemistry, vol.173, issue.11, pp.9895-9903, 2005.
DOI : 10.4049/jimmunol.173.2.855

F. F. Hamdan, Y. Percherancier, and M. Bouvier, Monitoring Protein-Protein Interactions in Living Cells by Bioluminescence Resonance Energy Transfer (BRET), Current Protocols in Neuroscience, vol.3, issue.1, 2006.
DOI : 10.1186/1472-6750-3-5

K. Levenberg, A method for the solution of certain non-linear problems in least squares, Quarterly of Applied Mathematics, vol.2, issue.2, pp.164-168, 1944.
DOI : 10.1090/qam/10666

E. Kobrinsky, L. Stevens, and N. M. Soldatov, 2.1 Potassium Channel Termini Associated with Voltage Gating, Journal of Biological Chemistry, vol.81, issue.28, pp.19233-19240, 2006.
DOI : 10.1074/jbc.M412140200

T. Rosenbaum, A. Gordon-shaag, and S. E. Gordon, /Calmodulin Modulates TRPV1 Activation by Capsaicin, The Journal of General Physiology, vol.22, issue.1, pp.53-62, 2004.
DOI : 10.1038/20200

URL : http://jgp.rupress.org/content/jgp/123/1/53.full.pdf

M. Numazaki, T. Tominaga, and M. Tominaga, Structural determinant of TRPV1 desensitization interacts with calmodulin, Proc. Natl. Acad. Sci. USA, pp.8002-8006, 2003.
DOI : 10.1111/j.1469-7793.2001.00813.x

W. Cheng, F. Yang, and J. Zheng, Thermosensitive TRPV Channel Subunits Coassemble into Heteromeric Channels with Intermediate Conductance and Gating Properties, The Journal of General Physiology, vol.337, issue.3, pp.191-207, 2007.
DOI : 10.1085/jgp.118.5.547

V. De-la-rosa, G. E. Rangel-yescas, and L. D. Islas, Coarse Architecture of the Transient Receptor Potential Vanilloid 1 (TRPV1) Ion Channel Determined by Fluorescence Resonance Energy Transfer, Journal of Biological Chemistry, vol.1783, issue.41, 2013.
DOI : 10.1002/jcc.20084

M. Liao, E. Cao, and Y. Cheng, Structure of the TRPV1 ion channel determined by electron cryo-microscopy, Nature, vol.14, issue.7478, pp.107-112, 2013.
DOI : 10.1016/S0263-7855(97)00009-X

R. Flynn, K. Chapman, and C. Altier, Targeting the Transient Receptor Potential Vanilloid Type 1 (TRPV1) Assembly Domain Attenuates Inflammation-induced Hypersensitivity, Journal of Biological Chemistry, vol.19, issue.24, pp.16675-16687, 2014.
DOI : 10.1096/fj.10-174433

J. F. Mercier, A. Salahpour, and M. Bouvier, -Adrenergic Receptor Homo- and Heterodimerization by Bioluminescence Resonance Energy Transfer, Journal of Biological Chemistry, vol.2, issue.47, pp.44925-44931, 2002.
DOI : 10.1161/01.RES.59.3.297

M. J. Caterina, M. A. Schumacher, and D. Julius, The capsaicin receptor: a heat-activated ion channel in the pain pathway, Nature, vol.389, pp.816-824, 1997.

Y. Cui, F. Yang, and J. Zheng, Selective disruption of high sensitivity heat activation but not capsaicin activation of TRPV1 channels by pore turret mutations, The Journal of General Physiology, vol.23, issue.4, pp.273-283, 2012.
DOI : 10.1016/S0092-8674(02)01013-9

P. Mcintyre, L. M. Mclatchie, and I. F. James, Pharmacological differences between the human and rat vanilloid receptor 1 (VR1) Br, 2001.

J. A. Matta and G. P. Ahern, Voltage is a partial activator of rat thermosensitive TRP channels, The Journal of Physiology, vol.400, issue.2, pp.469-482, 2007.
DOI : 10.1038/22761

V. Vlachová, A. Lyfenko, L. Vyklicky´, and . Vyklicky´, The effects of capsaicin and acidity on currents generated by noxious heat in cultured neonatal rat dorsal root ganglion neurones, The Journal of Physiology, vol.64, issue.3, pp.717-728, 2001.
DOI : 10.1111/j.1469-7793.1999.0181z.x

Y. C. Shin, S. Y. Shin, and J. H. Jeon, TRIP Database 2.0: A Manually Curated Information Hub for Accessing TRP Channel Interaction Network, PLoS ONE, vol.7, issue.10, p.47165, 2012.
DOI : 10.1371/journal.pone.0047165.g007

C. B. Phelps, R. R. Wang, and R. Gaudet, Differential Regulation of TRPV1, TRPV3, and TRPV4 Sensitivity through a Conserved Binding Site on the Ankyrin Repeat Domain, Journal of Biological Chemistry, vol.11, issue.1, pp.731-740, 2010.
DOI : 10.1093/nar/gki370

C. E. Deering-rice, V. K. Mitchell, and C. A. Reilly, Drofenine: a 2-APB analogue with greater selectivity for human TRPV3, Pharmacol . Res. Perspect, vol.2, p.62, 2014.

M. Jin, Z. Wu, and R. G. , Determinants of TRPV4 Activity following Selective Activation by Small Molecule Agonist GSK1016790A, PLoS ONE, vol.18, issue.2, p.16713, 2011.
DOI : 10.1371/journal.pone.0016713.g006

L. Bertrand, S. Parent, and L. Ménard, /ARRESTIN ASSAY IN STABLE RECOMBINANT CELLS: A PLATFORM TO SCREEN FOR COMPOUNDS THAT INTERACT WITH G PROTEIN-COUPLED RECEPTORS (GPCRS)*, Journal of Receptors and Signal Transduction, vol.22, issue.1-4, pp.533-541, 2002.
DOI : 10.1081/RRS-120014619

L. Zhang, F. Xu, and W. Min, Bioluminescence Assisted Switching and Fluorescence Imaging (BASFI), The Journal of Physical Chemistry Letters, vol.4, issue.22, pp.3897-3902, 2013.
DOI : 10.1021/jz402128j

B. Breton, E. ´. Sauvageau, and M. Bouvier, Multiplexing of Multicolor Bioluminescence Resonance Energy Transfer, Biophysical Journal, vol.99, issue.12, pp.4037-4046, 2010.
DOI : 10.1016/j.bpj.2010.10.025

D. M. Shcherbakova, M. A. Hink, and V. V. Verkhusha, An Orange Fluorescent Protein with a Large Stokes Shift for Single-Excitation Multicolor FCCS and FRET Imaging, Journal of the American Chemical Society, vol.134, issue.18, pp.7913-7923, 2012.
DOI : 10.1021/ja3018972

A. Takai, M. Nakano, and T. Nagai, Expanded palette of nanolanterns for real-time multicolor luminescence imaging, Proc. Natl, 2015.

J. Kusch and G. Zifarelli, Patch-Clamp Fluorometry: Electrophysiology meets Fluorescence, Biophysical Journal, vol.106, issue.6, pp.1250-1257, 2014.
DOI : 10.1016/j.bpj.2014.02.006

URL : https://doi.org/10.1016/j.bpj.2014.02.006

M. C. Trudeau and W. N. Zagotta, -Calmodulin???dependent Inhibition of Rod Cyclic Nucleotide-gated Channels Measured by Patch-clamp Fluorometry, The Journal of General Physiology, vol.23, issue.3, pp.211-223, 2004.
DOI : 10.1016/S0166-2236(00)01765-3

I. Derler, M. Hofbauer, and C. Romanin, -dependent inactivation, The Journal of Physiology, vol.95, issue.1, pp.31-44, 2006.
DOI : 10.1073/pnas.95.6.3287

S. Biswas, I. Deschênes, and G. F. Tomaselli, Calmodulin regulation of Nav1, 2008.

J. T. Gonçalves and W. St?-uhmer, Calmodulin Interaction with hEAG1 Visualized by FRET Microscopy, PLoS ONE, vol.7, issue.3, p.10873, 2010.
DOI : 10.1371/journal.pone.0010873.s003

K. D. Pfleger and K. A. Eidne, Illuminating insights into protein-protein interactions using bioluminescence resonance energy transfer (BRET), Nature Methods, vol.173, issue.3, pp.165-174, 2006.
DOI : 10.1016/S1389-1723(02)80234-1

G. C. Terstappen, R. Roncarati, and R. Peri, Screening technologies for ion channel drug discovery, Future Medicinal Chemistry, vol.4, issue.5, pp.715-730, 2010.
DOI : 10.1016/j.jneumeth.2008.10.007

J. M. Chambard, E. Tagat, and M. Partiseti, Transforming TRP Channel Drug Discovery Using Medium-Throughput Electrophysiological Assays, Journal of Biomolecular Screening, vol.67, issue.3, pp.468-477, 2014.
DOI : 10.1016/j.vascn.2012.10.005

H. B. Yu, M. Li, and X. L. Wang, High throughput screening technologies for ion channels, Acta Pharmacologica Sinica, vol.54, issue.1, pp.34-43, 2016.
DOI : 10.1177/1087057109348941

D. N. Robertson, R. Sleno, and G. Pineyro, Design and construction of conformational biosensors to monitor ion channel activation: A prototype FlAsH/BRET-approach to Kir3 channels, Methods, vol.92, pp.19-35, 2016.
DOI : 10.1016/j.ymeth.2015.07.011

P. V. Lishko, E. Procko, and R. Gaudet, The Ankyrin Repeats of TRPV1 Bind Multiple Ligands and Modulate Channel Sensitivity, Neuron, vol.54, issue.6, pp.905-918, 2007.
DOI : 10.1016/j.neuron.2007.05.027

S. Y. Lau, E. Procko, and R. Gaudet, ???calmodulin binding to N- and C-terminal regulatory regions of the TRPV1 channel, The Journal of General Physiology, vol.11, issue.5, pp.541-555, 2012.
DOI : 10.1007/s00424-005-1427-1

F. Yang, Y. Cui, and J. Zheng, Thermosensitive TRP channel pore turret is part of the temperature activation pathway, Proc. Natl, 2010.
DOI : 10.1007/s00232-008-9123-7

T. Voets, K. Talavera, and B. Nilius, Sensing with TRP channels, Nature Chemical Biology, vol.285, issue.2, pp.85-92, 2005.
DOI : 10.1038/84359

B. Nilius, K. Talavera, and T. Voets, Gating of TRP channels: a voltage connection?, The Journal of Physiology, vol.418, issue.1, pp.35-44, 2005.
DOI : 10.1038/nature00882

S. Galandrin, G. Oligny-longpré, and M. Bouvier, The evasive nature of drug efficacy: implications for drug discovery, Trends in Pharmacological Sciences, vol.28, issue.8, pp.423-430, 2007.
DOI : 10.1016/j.tips.2007.06.005

S. Stoilova-mcphie, S. Ali, and F. Laezza, Protein-protein interactions as new targets for ion channel drug discovery, Austin J. Pharmacol . Ther, vol.1, issue.2, p.5, 2013.

B. Storti, C. Di-rienzo, and F. Beltram, Unveiling TRPV1 spatiotemporal organization in live cell membranes, PLoS One, vol.10, p.116900, 2015.

X. Zhang, L. Li, and P. A. Mcnaughton, Proinflammatory Mediators Modulate the Heat-Activated Ion Channel TRPV1 via the Scaffolding Protein AKAP79/150, Neuron, vol.59, issue.3, pp.450-461, 2008.
DOI : 10.1016/j.neuron.2008.05.015

L. Li, R. Hasan, and X. Zhang, The Basal Thermal Sensitivity of the TRPV1 Ion Channel Is Determined by PKC??II, Journal of Neuroscience, vol.34, issue.24, pp.8246-8258, 2014.
DOI : 10.1523/JNEUROSCI.0278-14.2014

W. Cheng, C. Sun, and J. Zheng, Heteromerization of TRP channel subunits: extending functional diversity, Protein & Cell, vol.100, issue.9, pp.802-810, 2010.
DOI : 10.1073/pnas.1230540100

Y. Akao, Y. Nakagawa, and K. Akiyama, Arsenic trioxide induces apoptosis in neuroblastoma cell lines through the activation of caspase 3 in vitro, FEBS Letters, vol.391, issue.1-2, pp.59-62, 1999.
DOI : 10.1038/34112

M. Åkerfelt, R. I. Morimoto, and L. Sistonen, Heat shock factors: integrators of cell stress, development and lifespan, Nature Reviews Molecular Cell Biology, vol.14, issue.8, pp.545-555, 2010.
DOI : 10.1128/MCB.14.3.2087

P. Arockiasamy, M. , and S. , Design of compact electromagnetic impulse radiating antenna for melanoma treatment, Electromagnetic Biology and Medicine, vol.565, issue.2, pp.134-142, 2016.
DOI : 10.1109/LAWP.2010.2041027

L. Arredondo, H. B. Nelson, K. Beckingham, and M. Stern, Increased Transmitter Release and Aberrant Synapse Morphology in a Drosophila Calmodulin Mutant, Genetics, vol.150, pp.265-274, 1998.

R. Baan, Y. Grosse, B. Lauby-secretan, F. Ghissassi, V. Bouvard et al., Carcinogenicity of radiofrequency electromagnetic fields, The Lancet Oncology, vol.12, issue.7, pp.624-626, 2011.
DOI : 10.1016/S1470-2045(11)70147-4

URL : https://hal.archives-ouvertes.fr/ineris-00969545

D. Baez, N. Raddatz, G. Ferreira, C. Gonzalez, and R. Latorre, Gating of Thermally Activated Channels, Current Topics in Membranes, pp.51-87, 2014.
DOI : 10.1016/B978-0-12-800181-3.00003-8

G. Bhave, W. Zhu, H. Wang, D. J. Brasier, G. S. Oxford et al., cAMP-Dependent Protein Kinase Regulates Desensitization of the Capsaicin Receptor (VR1) by Direct Phosphorylation, Neuron, vol.35, issue.4, pp.721-731, 2002.
DOI : 10.1016/S0896-6273(02)00802-4

G. Bhave, H. Hu, K. S. Glauner, W. Zhu, H. Wang et al., Protein kinase C phosphorylation sensitizes but does not activate the capsaicin receptor transient receptor potential vanilloid 1 (TRPV1), Proc. Natl. Acad. Sci, pp.12480-12485, 2003.
DOI : 10.1074/jbc.M201551200

S. Brauchi, A Hot-Sensing Cold Receptor: C-Terminal Domain Determines Thermosensation in Transient Receptor Potential Channels, Journal of Neuroscience, vol.26, issue.18, pp.4835-4840, 2006.
DOI : 10.1523/JNEUROSCI.5080-05.2006

S. Brauchi, P. Orio, and R. Latorre, Clues to understanding cold sensation: Thermodynamics and electrophysiological analysis of the cold receptor TRPM8, Proc. Natl, 2004.
DOI : 10.1085/jgp.20028605

M. Breton and L. M. Mir, Microsecond and nanosecond electric pulses in cancer treatments, Bioelectromagnetics, vol.471, issue.2, pp.106-123, 2012.
DOI : 10.1016/j.abb.2007.12.009

Z. Bromberg, P. Goloubinoff, Y. Saidi, and Y. G. Weiss, The Membrane-Associated Transient Receptor Potential Vanilloid Channel Is the Central Heat Shock Receptor Controlling the Cellular Heat Shock Response in Epithelial Cells, PLoS ONE, vol.110, issue.3, p.57149, 2013.
DOI : 10.1371/journal.pone.0057149.g008

R. E. Campbell, O. Tour, A. E. Palmer, P. A. Steinbach, G. S. Baird et al., A monomeric red fluorescent protein, Proc. Natl. Acad. Sci. 99, pp.7877-7882, 2002.
DOI : 10.1107/S0021889891004399

E. Cao, M. Liao, Y. Cheng, J. , and D. , TRPV1 structures in distinct conformations reveal activation mechanisms, Nature, vol.297, issue.7478, pp.113-118, 2013.
DOI : 10.1006/jmbi.2000.3609

X. Cao, L. Ma, F. Yang, K. Wang, and J. Zheng, Divalent cations potentiate TRPV1 channel by lowering the heat activation threshold, The Journal of General Physiology, vol.57, issue.Suppl 3, pp.75-90, 2014.
DOI : 10.1002/cphy.c120001

R. A. Cardullo, Theoretical Principles and Practical Considerations for Fluorescence Resonance Energy Transfer Microscopy, In Methods in Cell Biology, pp.479-494, 2007.

K. Fuxe and E. I. Canela, Detection of heteromerization of more than two proteins by sequential BRET-FRET, Nat. Methods, vol.5, pp.727-733, 2008.

S. Chaudhury, M. Bal, S. Belugin, M. S. Shapiro, J. et al., AKAP150-Mediated TRPV1 Sensitization is Disrupted by Calcium/Calmodulin, Molecular Pain, vol.114, issue.6, pp.34-34, 2011.
DOI : 10.1016/S0006-3495(98)77976-7

H. Chuang, E. D. Prescott, H. Kong, S. Shields, S. Jordt et al., Bradykinin and nerve growth factor release the capsaicin receptor from PtdIns(4,5)P2-mediated inhibition, Nature, vol.395, issue.6840, pp.957-962, 2001.
DOI : 10.1038/27448

M. Chung, H. Lee, A. Mizuno, M. Suzuki, C. et al., TRPV3 and TRPV4 Mediate Warmth-evoked Currents in Primary Mouse Keratinocytes, Journal of Biological Chemistry, vol.286, issue.20, pp.21569-21575, 2004.
DOI : 10.1074/jbc.M301666200

D. E. Clapham, TRP channels as cellular sensors, Nature, vol.36, issue.6966, pp.517-524, 2003.
DOI : 10.1016/S0896-6273(02)01048-6

B. P. Cormack, R. H. Valdivia, and S. Falkow, FACS-optimized mutants of the green fluorescent protein (GFP), Gene, vol.173, issue.1, pp.33-38, 1996.
DOI : 10.1016/0378-1119(95)00685-0

D. Cosens and A. Manning, Abnormal Electroretinogram from a Drosophila Mutant, Nature, vol.5, issue.5216, pp.285-287, 1969.
DOI : 10.1016/0003-3472(67)90016-4

Y. Dai, TRPs and pain, Seminars in Immunopathology, vol.7, issue.3, pp.277-291, 2016.
DOI : 10.1186/1744-8069-7-41

C. C. Davis and Q. Balzano, The brain is not a radio receiver for wireless phone signals: Human tissue does not demodulate a modulated radiofrequency carrier, Comptes Rendus Physique, vol.11, issue.9-10, pp.585-591, 2010.
DOI : 10.1016/j.crhy.2010.09.002

D. Naidu, S. Dinkova-kostova, and A. T. , Regulation of the mammalian heat shock factor 1, The FEBS Journal, vol.33, issue.Suppl 1, pp.1606-1627, 2017.
DOI : 10.1093/molbev/msw054

A. De, A. M. Loening, and S. S. Gambhir, An Improved Bioluminescence Resonance Energy Transfer Strategy for Imaging Intracellular Events in Single Cells and Living Subjects, Cancer Research, vol.67, issue.15, 2007.
DOI : 10.1158/0008-5472.CAN-06-4623

A. De, P. Ray, A. M. Loening, and S. S. Gambhir, BRET3: a red-shifted bioluminescence resonance energy transfer (BRET)-based integrated platform for imaging protein-protein interactions from single live cells and living animals, The FASEB Journal, vol.23, issue.8, pp.2702-2709, 2009.
DOI : 10.1042/BJ20070803

A. S. Dhillon, S. Hagan, O. Rath, and W. Kolch, MAP kinase signalling pathways in cancer, Oncogene, vol.4, issue.22, pp.3279-3290, 2007.
DOI : 10.1158/0008-5472.CAN-05-0115

Y. Fang, Label-Free Biosensors for Cell Biology, International Journal of Electrochemistry, vol.1, issue.3-4, pp.1-16, 2011.
DOI : 10.1021/ac1007877

Y. Fang, G. G. Li, and J. Peng, Optical biosensor provides insights for bradykinin, 2005.

T. Förster, Zwischenmolekulare Energiewanderung und Fluoreszenz, Annalen der Physik, vol.2, issue.1-2, pp.55-75, 1948.
DOI : 10.1007/978-3-662-41791-1

M. Fosbrink, N. Aye-han, R. Cheong, A. Levchenko, and J. Zhang, Visualization of JNK activity dynamics with a genetically encoded fluorescent biosensor, Proc. Natl. Acad, 2010.
DOI : 10.1128/MCB.24.23.10145-10150.2004

K. R. Foster and R. Glaser, THERMAL MECHANISMS OF INTERACTION OF RADIOFREQUENCY ENERGY WITH BIOLOGICAL SYSTEMS WITH RELEVANCE TO EXPOSURE GUIDELINES, Health Physics, vol.92, issue.6, pp.609-620, 2007.
DOI : 10.1097/01.HP.0000262572.64418.38

K. R. Foster and M. H. Repacholi, Biological Effects of Radiofrequency Fields: Does Modulation Matter?, Radiation Research, vol.162, issue.2, pp.219-225, 2004.
DOI : 10.1667/RR3191

R. H. Funk, T. Monsees, and N. Özkucur, Electromagnetic effects ??? From cell biology to medicine, Progress in Histochemistry and Cytochemistry, vol.43, issue.4, pp.177-264, 2009.
DOI : 10.1016/j.proghi.2008.07.001

E. Galperin, V. V. Verkhusha, and A. Sorkin, Three-chromophore FRET microscopy to analyze multiprotein interactions in living cells, Nature Methods, vol.84, issue.3, pp.209-217, 2004.
DOI : 10.1073/pnas.192433499

F. P. De-gannes, E. Haro, A. Hurtier, M. Taxile, G. Ruffié et al., Effect of Exposure to the Edge Signal on Oxidative Stress in Brain Cell Models, Radiation Research, vol.175, issue.2, pp.225-230, 2011.
DOI : 10.1667/RR2320.1

URL : https://hal.archives-ouvertes.fr/hal-00573385

R. Gaudet, A primer on ankyrin repeat function in TRP channels and beyond, Molecular BioSystems, vol.21, issue.5, 2008.
DOI : 10.1016/j.bbapap.2005.06.005

I. Giaever and C. R. Keese, Monitoring fibroblast behavior in tissue culture with an applied electric field., Proc. Natl. Acad. Sci, pp.3761-3764, 1984.
DOI : 10.1073/pnas.81.12.3761

R. Glaser, Are thermoreceptors responsible for " non-thermal " effects of RF fields, 2005.

K. Hanaoka, F. Qian, A. Boletta, A. K. Bhunia, K. Piontek et al., Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents, Nature, vol.371, issue.6815, pp.990-994, 2000.
DOI : 10.1038/371516a0

Y. Hara, M. Wakamori, M. Ishii, E. Maeno, M. Nishida et al., LTRPC2 Ca2+-Permeable Channel Activated by Changes in Redox Status Confers Susceptibility to Cell Death, Molecular Cell, vol.9, issue.1, pp.163-173, 2002.
DOI : 10.1016/S1097-2765(01)00438-5

C. D. Harvey, A. G. Ehrhardt, C. Cellurale, H. Zhong, R. Yasuda et al., A genetically encoded fluorescent sensor of ERK activity, Proc. Natl. Acad. Sci. 105, pp.19264-19269, 2008.
DOI : 10.1186/1475-925X-2-13

R. Hasan, A. T. Leeson-payne, J. H. Jaggar, and X. Zhang, Calmodulin is responsible for Ca2+-dependent regulation of TRPA1 Channels, Scientific Reports, vol.26, p.45098, 2017.
DOI : 10.1016/j.neuron.2008.05.015

R. Heim, D. C. Prasher, and R. Y. And-tsien, Wavelength mutations and posttranslational autoxidation of green fluorescent protein., Proc. Natl. Acad. Sci. 91, pp.12501-12504, 1994.
DOI : 10.1073/pnas.91.26.12501

N. Hentze, L. Breton, L. Wiesner, J. Kempf, G. Mayer et al., Author response, eLife, vol.15, 2016.
DOI : 10.7554/eLife.11576.017

M. Heroux, M. Hogue, S. Lemieux, and M. Bouvier, Functional Calcitonin Generelated Peptide Receptors Are Formed by the Asymmetric Assembly of a Calcitonin Receptorlike Receptor Homo-oligomer and a Monomer of Receptor Activity-modifying Protein-1, J, 2007.

K. W. Ho, N. J. Ward, and D. J. Calkins, TRPV1: a stress response protein in the central nervous system, Am. J. Neurodegener. Dis, vol.1, issue.1, 2012.

T. Hofmann, V. Chubanov, T. Gudermann, and C. Montell, TRPM5 Is a Voltage-Modulated and Ca2+-Activated Monovalent Selective Cation Channel, Current Biology, vol.13, issue.13, pp.1153-1158, 2003.
DOI : 10.1016/S0960-9822(03)00431-7

H. Hu, Q. Gu, C. Wang, C. K. Colton, J. Tang et al., 2-Aminoethoxydiphenyl Borate Is a Common Activator of TRPV1, TRPV2, and TRPV3, Journal of Biological Chemistry, vol.269, issue.34, pp.35741-35748, 2004.
DOI : 10.1007/s004240100584

J. Huang, X. Zhang, and P. A. Mcnaughton, Modulation of temperature-sensitive TRP channels, Seminars in Cell & Developmental Biology, vol.17, issue.6, pp.638-645, 2006.
DOI : 10.1016/j.semcdb.2006.11.002

A. Jara-oseguera and L. D. Islas, The Role of Allosteric Coupling on Thermal Activation of Thermo-TRP Channels, Biophysical Journal, vol.104, issue.10, pp.2160-2169, 2013.
DOI : 10.1016/j.bpj.2013.03.055

N. A. Jeske, A. Diogenes, N. B. Ruparel, J. C. Fehrenbacher, M. Henry et al., A-kinase anchoring protein mediates TRPV1 thermal hyperalgesia through PKA phosphorylation of TRPV1, Pain, vol.138, issue.3, pp.604-616, 2008.
DOI : 10.1016/j.pain.2008.02.022

S. Jordt, J. , and D. , Molecular Basis for Species-Specific Sensitivity to ???Hot??? Chili Peppers, Cell, vol.108, issue.3, pp.421-430, 2002.
DOI : 10.1016/S0092-8674(02)00637-2

S. Jordt, M. Tominaga, J. , and D. , Acid potentiation of the capsaicin receptor determined by a key extracellular site, Proc. Natl. Acad. Sci. 97, pp.8134-8139, 2000.

R. P. Joshi and K. H. Schoenbach, Bioelectric effects of intense ultrashort pulses, 2010.

Y. Kaneko and A. Szallasi, Transient receptor potential (TRP) channels: a clinical perspective, British Journal of Pharmacology, vol.400, issue.10, pp.2474-2507, 2014.
DOI : 10.1038/22761

K. A. Kang, H. C. Lee, J. Lee, M. Hong, M. Park et al., Effects of combined radiofrequency radiation exposure on levels of reactive oxygen species in neuronal cells, Journal of Radiation Research, vol.52, issue.6, pp.265-276, 2014.
DOI : 10.1080/01926230290166724

E. Kobrinsky, 2.1 Potassium Channel Termini Associated with Voltage Gating, Journal of Biological Chemistry, vol.81, issue.28, pp.19233-19240, 2006.
DOI : 10.1074/jbc.M412140200

M. Kocan, H. B. See, R. M. Seeber, K. A. Eidne, and K. D. Pfleger, Demonstration of Improvements to the Bioluminescence Resonance Energy Transfer (BRET) Technology for the Monitoring of G Protein-Coupled Receptors in Live Cells, Journal of Biomolecular Screening, vol.13, issue.9, pp.888-898, 2008.
DOI : 10.1177/1087057108324032

I. Ahmed, R. Abd-alhameed, P. Excell, and V. Hodzic, Absence of nonlinear responses in cells and tissues exposed to RF energy at mobile phone frequencies using a doubly resonant cavity, Bioelectromagnetics, vol.31, pp.556-565, 2010.

R. Latorre, S. Brauchi, G. Orta, C. Zaelzer, and G. Vargas, ThermoTRP channels as modular proteins with allosteric gating. Calcium Channels Transp, pp.427-438, 2007.

P. V. Lishko, E. Procko, X. Jin, C. B. Phelps, and R. Gaudet, The Ankyrin Repeats of TRPV1 Bind Multiple Ligands and Modulate Channel Sensitivity, Neuron, vol.54, issue.6, pp.905-918, 2007.
DOI : 10.1016/j.neuron.2007.05.027

J. Liu and A. Escher, Improved assay sensitivity of an engineered secreted Renilla luciferase, Gene, vol.237, issue.1, pp.153-159, 1999.
DOI : 10.1016/S0378-1119(99)00314-5

B. Liu, K. Hui, and F. Qin, Thermodynamics of Heat Activation of Single Capsaicin Ion Channels VR1, Biophysical Journal, vol.85, issue.5, pp.2988-3006, 2003.
DOI : 10.1016/S0006-3495(03)74719-5

A. M. Loening, Consensus guided mutagenesis of Renilla luciferase yields enhanced stability and light output, Protein Engineering Design and Selection, vol.19, issue.9, pp.391-400, 2006.
DOI : 10.1093/protein/gzl023

P. Cormos and . Leveque, Dosimetric Characteristics of an EMF Delivery System Based on a Real-Time Impedance Measurement Device, IEEE Trans. Biomed. Eng, vol.63, pp.2317-2325, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01336811

J. A. Matta and G. P. Ahern, Voltage is a partial activator of rat thermosensitive TRP channels, The Journal of Physiology, vol.400, issue.2, pp.469-482, 2007.
DOI : 10.1038/22761

M. V. Matz, A. F. Fradkov, Y. A. Labas, A. P. Savitsky, A. G. Zaraisky et al., Erratum: Fluorescent proteins from nonbioluminescent Anthozoa species, Nature Biotechnology, vol.200, issue.10, 1999.
DOI : 10.1016/0003-2697(92)90279-G

M. H. Mccoy, W. , and E. , Use of electric cell-substrate impedance sensing as a tool for quantifying cytopathic effect in influenza A virus infected MDCK cells in real-time, Journal of Virological Methods, vol.130, issue.1-2, pp.157-161, 2005.
DOI : 10.1016/j.jviromet.2005.06.023

D. D. Mckemy, W. M. Neuhausser, J. , and D. , Identification of a cold receptor reveals a general role for TRP channels in thermosensation, Nature, vol.371, issue.6876, pp.52-58, 2002.
DOI : 10.1038/371519a0

J. P. Mcnamee and V. Chauhan, Radiofrequency Radiation and Gene/Protein Expression: A Review, Radiation Research, vol.172, issue.3, pp.265-287, 2009.
DOI : 10.1667/RR1726.1

A. Messeguer, R. Planells-cases, and A. Ferrer-montiel, Physiology and Pharmacology of the Vanilloid Receptor, Current Neuropharmacology, vol.4, issue.1, pp.1-15, 2006.
DOI : 10.2174/157015906775202995

L. M. Mir, S. Orlowski, J. J. Belehradek, and C. Paoletti, Electrochemotherapy potentiation of antitumour effect of bleomycin by local electric pulses, European Journal of Cancer and Clinical Oncology, vol.27, issue.1, pp.68-72, 1991.
DOI : 10.1016/0277-5379(91)90064-K

F. Mistretta, N. M. Buffi, G. Lughezzani, G. Lista, A. Larcher et al., Bladder Cancer and Urothelial Impairment: The Role of TRPV1 as Potential Drug Target, BioMed Research International, vol.368, issue.3, pp.1-10, 2014.
DOI : 10.1056/NEJMcibr1212341

N. Mochizuki, S. Yamashita, K. Kurokawa, Y. Ohba, T. Nagai et al., Spatio-temporal images of growth-factor-induced activation of Ras and Rap1, Nature, vol.58, issue.6841, pp.1065-1068, 2001.
DOI : 10.1016/S0091-679X(08)61960-3

D. P. Mohapatra and C. Nau, Desensitization of Capsaicin-activated Currents in the Vanilloid Receptor TRPV1 Is Decreased by the Cyclic AMP-dependent Protein Kinase Pathway, Journal of Biological Chemistry, vol.18, issue.50, pp.50080-50090, 2003.
DOI : 10.1111/j.1469-7793.1999.0721p.x

C. Montell, R. , and G. , Molecular characterization of the drosophila trp locus: A putative integral membrane protein required for phototransduction, Neuron, vol.2, issue.4, pp.1313-1323, 1989.
DOI : 10.1016/0896-6273(89)90069-X

C. Montell, K. Jones, E. Hafen, R. , and G. , Rescue of the Drosophila phototransduction mutation trp by germline transformation, Science, vol.230, issue.4729, pp.1040-1043, 1985.
DOI : 10.1126/science.3933112

M. M. Moran, M. A. Mcalexander, T. B-?-r-?, and A. Szallasi, Transient receptor potential channels as therapeutic targets, Nature Reviews Drug Discovery, vol.5, issue.8, pp.601-620, 2011.
DOI : 10.1038/nn942

S. M. Nauli, F. J. Alenghat, Y. Luo, E. Williams, P. Vassilev et al., Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells, Nature Genetics, vol.56, issue.2, pp.129-137, 2003.
DOI : 10.1046/j.1523-1755.1999.00659.x

S. R. Neves, Modeling of spatially-restricted intracellular signaling, Wiley Interdisciplinary Reviews: Systems Biology and Medicine, vol.7, issue.1, 2012.
DOI : 10.1371/journal.pbio.1000172

A. Nieto-posadas, A. Jara-oseguera, and T. Rosenbaum, TRP Channel Gating Physiology, Current Topics in Medicinal Chemistry, vol.11, issue.17, pp.2131-2150, 2011.
DOI : 10.2174/156802611796904870

O. Pänke, W. Weigel, S. Schmidt, A. Steude, and A. A. Robitzki, A cell-based impedance assay for monitoring transient receptor potential (TRP) ion channel activity, Biosensors and Bioelectronics, vol.26, issue.5, 2011.
DOI : 10.1016/j.bios.2010.10.015

A. M. Peier, A. Moqrich, A. C. Hergarden, A. J. Reeve, D. A. Andersson et al., A TRP Channel that Senses Cold Stimuli and Menthol, Cell, vol.108, issue.5, pp.705-715, 2002.
DOI : 10.1016/S0092-8674(02)00652-9

URL : https://hal.archives-ouvertes.fr/hal-00311323

A. Pelletier, S. Delanaud, P. Thuroczy, G. De-seze, R. Cerri et al., Effects of chronic exposure to radiofrequency electromagnetic fields on energy balance in developing rats, Environmental Science and Pollution Research, vol.60, issue.5, pp.2735-2746, 2013.
DOI : 10.1139/y82-057

URL : https://hal.archives-ouvertes.fr/ineris-00963429

A. Pelletier, S. Delanaud, R. De-seze, V. Bach, J. Libert et al., Does Exposure to a Radiofrequency Electromagnetic Field Modify Thermal Preference in Juvenile Rats?, PLoS ONE, vol.139, issue.6, p.99007, 2014.
DOI : 10.1371/journal.pone.0099007.s002

A. Perálvarez-marín, P. Doñate-macian, and R. Gaudet, What do we know about the transient receptor potential vanilloid 2 (TRPV2) ion channel?, FEBS Journal, vol.38, issue.21, pp.5471-5487, 2013.
DOI : 10.1093/nar/gkq399

C. B. Phelps, R. R. Wang, S. S. Choo, and R. Gaudet, Differential Regulation of TRPV1, TRPV3, and TRPV4 Sensitivity through a Conserved Binding Site on the Ankyrin Repeat Domain, Journal of Biological Chemistry, vol.11, issue.1, pp.731-740, 2010.
DOI : 10.1093/nar/gki370

W. F. Pickard and Y. H. Barsoum, Radio-frequency bioeffects at the membrane level: Separation of thermal and athermal contributions in the characeae, The Journal of Membrane Biology, vol.247, issue.1, pp.39-54, 1981.
DOI : 10.1016/B978-0-12-027908-1.50008-6

I. S. Ramsey, M. Delling, and D. E. Clapham, AN INTRODUCTION TO TRP CHANNELS, Annual Review of Physiology, vol.68, issue.1, pp.619-647, 2006.
DOI : 10.1146/annurev.physiol.68.040204.100431

T. Rosenbaum, A. Gordon-shaag, M. Munari, G. , and S. E. , /Calmodulin Modulates TRPV1 Activation by Capsaicin, The Journal of General Physiology, vol.22, issue.1, pp.53-62, 2004.
DOI : 10.1038/20200

URL : http://jgp.rupress.org/content/jgp/123/1/53.full.pdf

I. Sarria, J. Ling, M. X. Zhu, and J. G. Gu, : distinction from tachyphylaxis, Journal of Neurophysiology, vol.270, issue.6, pp.3056-3066, 2011.
DOI : 10.1038/nn1843

A. R. Sheppard, M. L. Swicord, and Q. Balzano, QUANTITATIVE EVALUATIONS OF MECHANISMS OF RADIOFREQUENCY INTERACTIONS WITH BIOLOGICAL MOLECULES AND PROCESSES, Health Physics, vol.95, issue.4, pp.365-396, 2008.
DOI : 10.1097/01.HP.0000319903.20660.37

S. Shrestha and S. K. Deo, Anthozoa red fluorescent protein in biosensing, Analytical and Bioanalytical Chemistry, vol.100, issue.2, 2006.
DOI : 10.1021/cr990115p

N. M. Shupak, F. S. Prato, and A. W. Thomas, Therapeutic uses of pulsed magneticfield exposure: a review, Radio Sci Bull, vol.307, pp.9-30, 2003.

J. A. Stolwijk, K. Matrougui, C. W. Renken, and M. Trebak, Impedance analysis of GPCR-mediated changes in endothelial barrier function: overview and fundamental considerations for stable and reproducible measurements, Pfl??gers Archiv - European Journal of Physiology, vol.748, issue.6, pp.2193-2218, 2015.
DOI : 10.1111/j.1749-6632.1994.tb17311.x

L. Su, X. Wei, Z. Xu, C. , and G. , RF-EMF exposure at 1800???MHz did not elicit DNA damage or abnormal cellular behaviors in different neurogenic cells, Bioelectromagnetics, vol.12, issue.3, pp.175-185, 2017.
DOI : 10.1186/s12974-015-0300-1

A. Szallasi and P. M. Blumberg, Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analog of capsaicin, the irritant constituent in red pepper, Neuroscience, vol.30, issue.2, pp.515-520, 1989.
DOI : 10.1016/0306-4522(89)90269-8

B. I. Tóth, A. Oláh, A. G. Szöll?si, and T. Bíró, TRP channels in the skin, British Journal of Pharmacology, vol.1, issue.Suppl 1, pp.2568-2581, 2014.
DOI : 10.4161/derm.1.5.9499

C. Creminon, P. Geppetti, H. , and S. , Hydrogen sulfide causes vanilloid receptor 1-mediated neurogenic inflammation in the airways, Br. J. Pharmacol, vol.145, pp.1123-1131, 2005.

R. Y. Tsien, THE GREEN FLUORESCENT PROTEIN, Annual Review of Biochemistry, vol.67, issue.1, pp.509-544, 1998.
DOI : 10.1146/annurev.biochem.67.1.509

L. Vay, C. Gu, and P. A. Mcnaughton, The thermo-TRP ion channel family: properties and therapeutic implications, British Journal of Pharmacology, vol.10, issue.4, pp.787-801, 2012.
DOI : 10.1038/nn1843

K. Venkatachalam and C. Montell, TRP Channels, Annual Review of Biochemistry, vol.76, issue.1, pp.387-417, 2007.
DOI : 10.1146/annurev.biochem.75.103004.142819

R. Vennekens, J. Vriens, and B. Nilius, Herbal Compounds and Toxins Modulating TRP Channels, Current Neuropharmacology, vol.6, issue.1, pp.79-96, 2008.
DOI : 10.2174/157015908783769644

URL : http://europepmc.org/articles/pmc2645550?pdf=render

L. Verschaeve, Evaluations of international expert group reports on the biological effects of radiofrequency fields, 2012.

L. Verschaeve, J. Juutilainen, I. Lagroye, J. Miyakoshi, R. Saunders et al., In vitro and in vivo genotoxicity of radiofrequency fields, Mutation Research/Reviews in Mutation Research, vol.705, issue.3, pp.252-268, 2010.
DOI : 10.1016/j.mrrev.2010.10.001

URL : https://hal.archives-ouvertes.fr/hal-00573541

S. W. Vetter and E. Leclerc, Novel aspects of calmodulin target recognition and activation, European Journal of Biochemistry, vol.268, issue.3, pp.404-414, 2003.
DOI : 10.1073/pnas.79.10.3162

A. Vihervaara and L. Sistonen, HSF1 at a glance, Journal of Cell Science, vol.127, issue.2, pp.261-266, 2014.
DOI : 10.1242/jcs.132605

J. D. Violin, J. Zhang, R. Y. Tsien, and A. C. Newton, A genetically encoded fluorescent reporter reveals oscillatory phosphorylation by protein kinase C, The Journal of Cell Biology, vol.10, issue.2, pp.899-909, 2003.
DOI : 10.1073/pnas.211566798

J. Vriens, H. Watanabe, A. Janssens, G. Droogmans, T. Voets et al., Cell swelling, heat, and chemical agonists use distinct pathways for the activation of the cation channel TRPV4, Proc. Natl. Acad. Sci, pp.396-401, 2004.
DOI : 10.1073/pnas.100129497

K. M. Walker, The VR1 Antagonist Capsazepine Reverses Mechanical Hyperalgesia in Models of Inflammatory and Neuropathic Pain, Journal of Pharmacology and Experimental Therapeutics, vol.304, issue.1, pp.56-62, 2003.
DOI : 10.1124/jpet.102.042010

K. Wirkner, H. Hognestad, R. Jahnel, F. Hucho, and P. Illes, Characterization of rat transient receptor potential vanilloid 1 receptors lacking the N-glycosylation site N604, NeuroReport, vol.16, issue.9, 2005.
DOI : 10.1097/00001756-200506210-00023

B. Xing, Y. Yang, J. Du, H. Chen, C. Qi et al., Cyclin-Dependent Kinase 5 Controls TRPV1 Membrane Trafficking and the Heat Sensitivity of Nociceptors through KIF13B, Journal of Neuroscience, vol.32, issue.42, pp.14709-14721, 2012.
DOI : 10.1523/JNEUROSCI.1634-12.2012

F. Yang, Y. Cui, K. Wang, and J. Zheng, Thermosensitive TRP channel pore turret is part of the temperature activation pathway, Proc. Natl. Acad. Sci, pp.7083-7088, 2010.
DOI : 10.1007/s00232-008-9123-7

Q. Zeng, G. Chen, Y. Weng, L. Wang, H. Chiang et al., Effects of Global System for Mobile Communications 1800 MHz radiofrequency electromagnetic fields on gene and protein expression in MCF-7 cells, PROTEOMICS, vol.519, issue.17, pp.4732-4738, 2006.
DOI : 10.1016/S1383-5718(02)00109-2

X. Zhang, J. Huang, and P. A. Mcnaughton, NGF rapidly increases membrane expression of TRPV1 heat-gated ion channels, The EMBO Journal, vol.19, issue.24, pp.4211-4223, 2005.
DOI : 10.1523/JNEUROSCI.2893-04.2004

J. Zheng, Molecular Mechanism of TRP Channels, Comprehensive Physiology, R, 2013.
DOI : 10.1038/22761

X. Zhu, B. P. Chu, M. Peyton, and L. Birnbaumer, gene, FEBS Letters, vol.267, issue.3, pp.193-198, 1995.
DOI : 10.1126/science.7809622

URL : https://hal.archives-ouvertes.fr/hal-00973804