D. Marguet, P. F. Lenne, H. Rigneault, and H. T. He, Dynamics in the plasma membrane: how to combine fluidity and order, The EMBO Journal, vol.81, issue.15, pp.3446-3457, 2006.
DOI : 10.1103/PhysRevLett.82.4014

URL : https://hal.archives-ouvertes.fr/hal-00103897

C. Manzo and M. F. Garcia-parajo, A review of progress in single particle tracking: from methods to biophysical insights, Reports on Progress in Physics, vol.78, issue.12, p.124601, 2015.
DOI : 10.1088/0034-4885/78/12/124601

X. Michalet, Mean square displacement analysis of single-particle trajectories with localization error: Brownian motion in an isotropic medium, Physical Review E, vol.82, issue.4, p.41914, 2010.
DOI : 10.1103/PhysRevE.82.011917

X. Michalet and A. J. Berglund, Optimal diffusion coefficient estimation in single-particle tracking, Physical Review E, vol.16, issue.6, p.61916, 2012.
DOI : 10.1109/TASSP.1984.1164399

D. Choquet and A. Triller, The Dynamic Synapse, Neuron, vol.80, issue.3, pp.691-703, 2013.
DOI : 10.1016/j.neuron.2013.10.013

URL : https://doi.org/10.1016/j.neuron.2013.10.013

C. Ribrault, J. Reingruber, M. Petkovic, T. Galli, N. E. Ziv et al., Syntaxin1A Lateral Diffusion Reveals Transient and Local SNARE Interactions, Journal of Neuroscience, vol.31, issue.48, pp.17590-17602, 2011.
DOI : 10.1523/JNEUROSCI.4065-11.2011

URL : https://hal.archives-ouvertes.fr/hal-00658260

M. Renner, D. Choquet, and A. Triller, Control of the Postsynaptic Membrane Viscosity, Journal of Neuroscience, vol.29, issue.9, pp.2926-2937, 2009.
DOI : 10.1523/JNEUROSCI.4445-08.2009

T. C. Jacob, Y. D. Bogdanov, C. Magnus, R. S. Saliba, J. T. Kittler et al., Gephyrin Regulates the Cell Surface Dynamics of Synaptic GABAA Receptors, Journal of Neuroscience, vol.25, issue.45, pp.10469-78, 2005.
DOI : 10.1523/JNEUROSCI.2267-05.2005

W. Lu, H. Man, W. Ju, W. S. Trimble, J. F. Macdonald et al., Activation of Synaptic NMDA Receptors Induces Membrane Insertion of New AMPA Receptors and LTP in Cultured Hippocampal Neurons, Neuron, vol.29, issue.1, pp.243-254, 2001.
DOI : 10.1016/S0896-6273(01)00194-5

A. Kamal, G. M. Ramakers, I. J. Urban, P. N. De-graan, and W. H. Gispen, Chemical LTD in the CA1 field of the hippocampus from young and mature rats, European Journal of Neuroscience, vol.20, issue.10, pp.3512-35161411, 1999.
DOI : 10.1016/S0166-2236(96)01023-5

G. Giannone, E. Hosy, F. Levet, A. Constals, K. Schulze et al., Dynamic Superresolution Imaging of Endogenous Proteins on Living Cells at Ultra-High Density, Biophysical Journal, vol.99, issue.4, pp.1303-1313, 2010.
DOI : 10.1016/j.bpj.2010.06.005

URL : https://hal.archives-ouvertes.fr/hal-00661871

M. V. Ehrensperger, C. Hanus, C. Vannier, A. Triller, and M. Dahan, Multiple Association States between Glycine Receptors and Gephyrin Identified by SPT Analysis, Biophysical Journal, vol.92, issue.10, pp.3706-3718, 2007.
DOI : 10.1529/biophysj.106.095596

M. Renner, Y. Domanov, F. Sandrin, I. Izeddin, P. Bassereau et al., Lateral Diffusion on Tubular Membranes: Quantification of Measurements Bias, PLoS ONE, vol.5, issue.9, p.25731, 2011.
DOI : 10.1371/journal.pone.0025731.s006

M. J. Saxton and K. Jacobson, Single Particle Tracking, Annu. Rev. Biophys. Biomol. Struct, vol.26, pp.373-399, 1997.
DOI : 10.1007/978-1-59745-397-4_6

A. Kusumi, Y. Sako, and M. Yamamoto, Confined lateral diffusion of membrane receptors as studied by single particle tracking (nanovid microscopy). Effects of calcium-induced differentiation in cultured epithelial cells, Meroz, Y. and I.M. Sokolov. 2015. A Toolbox for Determining Subdiffusive Mechanisms, pp.2021-20401, 1993.
DOI : 10.1016/S0006-3495(93)81253-0

R. Simson, E. D. Sheets, and K. Jacobson, Detection of temporary lateral confinement of membrane proteins using single-particle tracking analysis, Biophysical Journal, vol.69, issue.3, pp.989-993, 1995.
DOI : 10.1016/S0006-3495(95)79972-6

H. Qian, M. P. Sheetz, and E. L. Elson, Single particle tracking. Analysis of diffusion and flow in two-dimensional systems, Biophysical Journal, vol.60, issue.4, pp.910-921, 1991.
DOI : 10.1016/S0006-3495(91)82125-7

N. Meilhac, L. Le-guyader, L. Salome, L. , and N. Destainville, Detection of confinement and jumps in single-molecule membrane trajectories Trajectory analysis of single molecules exhibiting non-brownian motion, Phys. Rev. E Stat. Nonlin. Soft Matter Phys. Phys. Chem. Chem. Phys, vol.7313, pp.119154326-119154360, 2006.

S. Matsuoka, T. Shibata, and M. Ueda, Statistical Analysis of Lateral Diffusion and Multistate Kinetics in Single-Molecule Imaging, Biophysical Journal, vol.97, issue.4, pp.1115-1124, 2009.
DOI : 10.1016/j.bpj.2009.06.007

V. Rajani, G. Carrero, D. E. Golan, G. De-vries, and C. W. Cairo, Analysis of Molecular Diffusion by First-Passage Time Variance Identifies the Size of Confinement Zones, Biophysical Journal, vol.100, issue.6, pp.1463-1472, 2011.
DOI : 10.1016/j.bpj.2011.01.064

Y. M. Umemura, M. Vrljic, S. Y. Nishimura, T. K. Fujiwara, K. G. Suzuki et al., Both MHC Class II and its GPI-Anchored Form Undergo Hop Diffusion as Observed by Single-Molecule Tracking, Biophysical Journal, vol.95, issue.1, pp.435-450, 2008.
DOI : 10.1529/biophysj.107.123018

URL : https://doi.org/10.1529/biophysj.107.123018

D. Goswami, K. Gowrishankar, S. Bilgrami, S. Ghosh, R. Raghupathy et al., Nanoclusters of GPI-Anchored Proteins Are Formed by Cortical Actin-Driven Activity, Cell, vol.135, issue.6, pp.1085-1097, 2008.
DOI : 10.1016/j.cell.2008.11.032

K. Ritchie, X. Y. Shan, J. Kondo, K. Iwasawa, T. Fujiwara et al., Detection of Non-Brownian Diffusion in the Cell Membrane in Single Molecule Tracking, Biophysical Journal, vol.88, issue.3, pp.2266-2277, 2005.
DOI : 10.1529/biophysj.104.054106

A. Triller and D. Choquet, New Concepts in Synaptic Biology Derived from Single-Molecule Imaging, Neuron, vol.59, issue.3, pp.359-374, 2008.
DOI : 10.1016/j.neuron.2008.06.022

J. M. Henley and K. A. Wilkinson, Synaptic AMPA receptor composition in development, plasticity and disease, Nature Reviews Neuroscience, vol.20, issue.6, pp.337-350, 2016.
DOI : 10.1038/nature06995

M. Renner, C. Schweizer, H. Bannai, A. Triller, A. et al., Diffusion barriers constrain receptors at synapses. PLoS One.7:e43032. 30 Unified quantitative model of AMPA receptor trafficking at synapses, PNAS, vol.109, pp.3522-3527, 2012.
DOI : 10.1371/journal.pone.0043032

URL : https://doi.org/10.1371/journal.pone.0043032

M. L. Renner, L. Cognet, B. Lounis, A. Triller, and D. Choquet, The excitatory postsynaptic density is a size exclusion diffusion environment, Neuropharmacology, vol.56, issue.1, pp.30-36, 2009.
DOI : 10.1016/j.neuropharm.2008.07.022

URL : https://hal.archives-ouvertes.fr/hal-00506460

T. P. Li, Y. Song, H. D. Macgillavry, T. A. Blanpied, and S. Raghavachari, Protein Crowding within the Postsynaptic Density Can Impede the Escape of Membrane Proteins, Journal of Neuroscience, vol.36, issue.15, pp.4276-4295, 2016.
DOI : 10.1523/JNEUROSCI.3154-15.2016

M. C. Ashby, S. R. Maier, A. Nishimune, and J. M. Henley, Lateral Diffusion Drives Constitutive Exchange of AMPA Receptors at Dendritic Spines and Is Regulated by Spine Morphology, Journal of Neuroscience, vol.26, issue.26, pp.7046-7055, 2006.
DOI : 10.1523/JNEUROSCI.1235-06.2006

L. Huganir, D. Cognet, and . Choquet, Surface mobility of postsynaptic AMPARs tunes synaptic transmission, Science, vol.320, pp.201-205, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00747627

A. Constals, A. C. Penn, B. Compans, E. Toulme, A. Phillipat et al., Glutamate-Induced AMPA Receptor Desensitization Increases Their Mobility and Modulates Short-Term Plasticity through Unbinding from Stargazin, Neuron, vol.85, issue.4, pp.787-803, 2015.
DOI : 10.1016/j.neuron.2015.01.012

URL : https://doi.org/10.1016/j.neuron.2015.01.012

T. E. Chater, Y. Goda-kasai, R. S. , and A. Kusumi, The role of AMPA receptors in postsynaptic mechanisms of synaptic plasticity. Front Single-molecule imaging revealed dynamic GPCR dimerization, Cell Neurosci. Curr. Opin. Cell Biol, vol.8, issue.27, pp.401-438, 2014.

A. Dahan and . Triller, Quantitative nanoscopy of inhibitory synapses: counting gephyrin molecules and receptor binding sites, Neuron, vol.79, pp.308-321, 2013.

G. Gouzer, C. G. Specht, L. Allain, T. Shinoe, and A. Triller, Benzodiazepine-dependent stabilization of GABAA receptors at synapses, Molecular and Cellular Neuroscience, vol.63, pp.101-114, 2014.
DOI : 10.1016/j.mcn.2014.10.004

M. Triller and . Kneussel, Radixin regulates synaptic GABAA receptor density and is essential for reversal learning and short-term memory, Nat. Commun, vol.6, p.6872, 2015.