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The structure and function of G-protein-coupled receptors
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G-protein-coupled receptors (GPCRs) mediate most of our physiological responses to hormones, neurotransmitters and environmental stimulants, and so have great potential as therapeutic targets for a broad spectrum of diseases. They are also fascinating molecules from the perspective of membrane-protein structure and biology. Great progress has been made over the past three decades in understanding diverse GPCRs, from pharmacology to functional characterization in vivo. Recent high-resolution structural studies have provided insights into the molecular mechanisms of GPCR activation and constitutive activity.
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“GPR20 belongs to the family of the G-protein-coupled receptors, which participate in intracellular second messenger systems triggered by different hormones and neurotransmitters, and amyloid β.53, 54, 55”
From APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer’s disease (2016) · cites this paper as [54]
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“Both theoretical and experimental results do not offer any clear conclusions with respect to the vibrational theory of neurotransmission for adenosine, serotonin and histamine receptors and their related ligands.”
From Quantum effects in the brain: A review (2020) · cites this paper as [115]
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“Understanding the mechanism or mechanisms of ligand-GPCR interaction is particularly important due to the fact that GPCRs are a major drug target associated with one third of all pharmaceuticals 103,115 .”
From Quantum effects in the brain: A review (2020) · cites this paper as [115]
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Crystal Structure of Rhodopsin: A G Protein-Coupled Receptor
Palczewski, K., Kumasaka, T., Hori, T., Behnke, C. A., Motoshima, H., Fox, B. A., Trong, I. L., Teller, D. C., Okada, T., Stenkamp, R. E., et al. (2000) · Science · doi:10.1126/science.289.5480.739 · Cited by 5,637
High-Resolution Crystal Structure of an Engineered Human β 2 -Adrenergic G Protein–Coupled Receptor
Cherezov, V., Rosenbaum, D. M., Hanson, M. A., Rasmussen, S. G. F., Thian, F. S., Kobilka, T. S., Choi, H., Kühn, P., Weis, W. I., Kobilka, B. K., et al. (2007) · Science · doi:10.1126/science.1150577 · Cited by 3,280
Self-citationBallesteros, J. A., & Weinstein, H. (1995) · Methods in neurosciences · doi:10.1016/s1043-9471(05)80049-7 · Cited by 3,001 · cited 1×
“48 (human β 2 AR, with Ballesteros/Weinstein numberin”
Fredriksson, R., Lagerström, M. C., Lundin, L.-G., & Schiöth, H. B. (2003) · Molecular Pharmacology · doi:10.1124/mol.63.6.1256 · Cited by 2,941 · cited 1×
“GPCRs in vertebrates are commonly divided into five families on the basis of their sequence and structural similarity”
Crystal structure of the human β2 adrenergic G-protein-coupled receptor
Rasmussen, S. G. F., Choi, H., Rosenbaum, D. M., Kobilka, T. S., Thian, F. S., Edwards, P. C., Burghammer, M. C., Ratnala, V. R. P., Sanishvili, R., Fischetti, R. F., et al. (2007) · Nature · doi:10.1038/nature06325 · Cited by 1,935
Self-citationThe 2.6 Angstrom Crystal Structure of a Human A 2A Adenosine Receptor Bound to an Antagonist
Jaakola, V., Griffith, M. T., Hanson, M. A., Cherezov, V., Chien, E. Y. T., Lane, J. R., IJzerman, A. P., & Stevens, R. C. (2008) · Science · doi:10.1126/science.1164772 · Cited by 1,786
Léan, A. D., Stadel, J. M., & Lefkowitz, R. J. (1980) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)79672-9 · Cited by 1,606
Structure of a β1-adrenergic G-protein-coupled receptor
Warne, T., Serrano‐Vega, M. J., Baker, J. G., Moukhametzianov, R., Edwards, P. C., Henderson, R. A., Leslie, A. G. W., Tate, C. G., & Schertler, G. F. X. (2008) · Nature · doi:10.1038/nature07101 · Cited by 1,377
GPCR Engineering Yields High-Resolution Structural Insights into β 2 -Adrenergic Receptor Function
Rosenbaum, D. M., Cherezov, V., Hanson, M. A., Rasmussen, S. G. F., Thian, F. S., Kobilka, T. S., Choi, H., Yao, X.-J., Weis, W. I., Stevens, R. C., et al. (2007) · Science · doi:10.1126/science.1150609 · Cited by 1,335
Self-citationCloning of the gene and cDNA for mammalian β-adrenergic receptor and homology with rhodopsin
Dixon, R. A. F., Kobilka, B. K., Strader, D. J., Benovic, J., Dohlman, H. G., Frielle, T., Bolanowski, M. A., Bennett, C. D., Rands, E., Diehl, R. E., et al. (1986) · Nature · doi:10.1038/321075a0 · Cited by 1,275 · cited 1×
“The clustering of these residues in the cytoplasmic half of the transmembrane bundle reflects the basic conservation of mechanism across GPCRs, a remarkable structural affirmation of a hypothesis made more than 20 years ag”
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Xie, N.-N., Wu, C., Ge, Q., Zhou, J., Long, F., Mao, Q., Li, S., & Shen, H. (2022) · Food & Function · doi:10.1039/d2fo03383f · Cited by 29
D’Amore, V. M., Conflitti, P., Marinelli, L., & Limongelli, V. (2024) · Chem · doi:10.1016/j.chempr.2024.08.004 · Cited by 27
Activity of GPCR-targeted drugs influenced by human gut microbiota metabolism
Wu, Q., Song, D., Zhao, Y., Verdegaal, A. A., Turocy, T., Lowey, B., Goodman, A. L., Palm, N. W., & Crawford, J. M. (2025) · Nature Chemistry · doi:10.1038/s41557-025-01789-w · Cited by 28
“G-protein-coupled receptors (GPCRs) are a large family of cell surface receptors that transduce external chemical information into cellular signalling outcomes and participate in a diversity of disease-associated pathways 1 .”
Kuwasako, K., Kitamura, K., Nagata, S., Hikosaka, T., & Kato, J. (2010) · Peptides · doi:10.1016/j.peptides.2010.10.005 · Cited by 30
Reyes, B. A. S., Bangasser, D. A., Valentino, R. J., & Bockstaele, E. J. V. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.07.017 · Cited by 28
Effects of elevated ammonium on the transcriptome of the stony coral Pocillopora damicornis
Yuan, C., Zhou, Z., Zhang, Y., Chen, G., Yu, X., Ni, X., Tang, J., & Huang, B. (2016) · Marine Pollution Bulletin · doi:10.1016/j.marpolbul.2016.08.036 · Cited by 28
Single-cell profiling reveals GPCR heterogeneity and functional patterning during neuroinflammation
Tischner, D., Grimm, M., Kaur, H., Staudenraus, D., Carvalho, J., Looso, M., Günther, S., Wanke, F., Moos, S., Siller, N., et al. (2017) · JCI Insight · doi:10.1172/jci.insight.95063 · Cited by 26
A Comparison of the Primary Sensory Neurons Used in Olfaction and Vision
Lankford, C. K., Laird, J. G., Inamdar, S. M., & Baker, S. A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.595523 · Cited by 27
“GPCRs are characterized by their serpentine structure consisting of an extracellular N-terminus, seven transmembrane domains, and a cytoplasmic C-terminus (Rosenbaum et al., 2009).”
BackgroundZhou, T., Liu, Z., Pei, J., Pan, D., Gao, X., Dang, Y., & Zhao, Y. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c02985 · Cited by 28
Pulmonary neuroendocrine cells sense succinate to stimulate myoepithelial cell contraction
Yu, W., Moninger, T. O., Rector, M. V., Stoltz, D. A., & Welsh, M. J. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.08.010 · Cited by 27
Structure and function meet at the nicotinic acetylcholine receptor-lipid interface
Barrantes, F. J. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106729 · Cited by 31
FFA1‐selective agonistic activity based on docking simulation using FFA1 and GPR120 homology models
Takeuchi, M., Hirasawa, A., Hara, T., Kimura, I., Hirano, T., Suzuki, T., Miyata, N., Awaji, T., Ishiguro, M., & Tsujimoto, G. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.02052.x · Cited by 28
Singh, P., Haldar, S., & Chattopadhyay, A. (2012) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2012.11.022 · Cited by 29
Umanah, G. K. E., Huang, L.-Y., Ding, F., Arshava, B. M., Farley, A. R., Link, A. J., Naider, F. R., & Becker, J. M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.149500 · Cited by 28
Zhang, X., Wang, W., Bedigian, A. V., Coughlin, M. L., Mitchison, T. J., & Eggert, U. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207821109 · Cited by 28
Defining the membrane proteome of NK cells
Ghosh, D., Lippert, D. N. D., Krokhin, O. V., Cortens, J. P., & Wilkins, J. A. (2009) · Journal of Mass Spectrometry · doi:10.1002/jms.1696 · Cited by 30
“[85 – 87] These complexes are often transient but during the period of contact they are stable as evidenced by the capacity to physically isolate them such as G-protein coupled receptors[88] or signaling molecules (Lyn[89,90] and ZAP70[91 – 93]).”
BackgroundKleinau, G., Hoyer, I., Kreuchwig, A., Haas, A., Rutz, C., Furkert, J., Worth, C. L., Krause, G., & Schülein, R. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.196980 · Cited by 28
Belloir, C., Miller, M.-L., Neiers, F., Briand, L. V., & Bon, A. L. (2016) · Protein Expression and Purification · doi:10.1016/j.pep.2016.09.006 · Cited by 28
A closer look into the α-helix basin
Haimov, B., & Srebnik, S. (2016) · Scientific Reports · doi:10.1038/srep38341 · Cited by 28
Zheng, J., Cao, J., Mao, Y., Su, Y., & Wang, J. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.05.030 · Cited by 28
Singh, K. D., Ünal, H., Desnoyer, R. W., & Karnik, S. S. (2019) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.8b00583 · Cited by 29
G-protein Coupled Receptors in Stem Cell Self-Renewal and Differentiation
Kobayashi, N., Hawes, S. M., Crook, J. M., & Pébay, A. (2010) · Stem Cell Reviews and Reports · doi:10.1007/s12015-010-9167-9 · Cited by 30
New Insights into GPCR Function: Implications for HTS
Eglen, R. M., & Reisine, T. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-317-6_1 · Cited by 28
Oxytocin receptor behavioral effects and cell types in the bed nucleus of the stria terminalis
Luo, P. X., Zakharenkov, H. C., Torres, L. Y., Rios, R. A., Gegenhuber, B., Black, A. M., Xu, C. K., Minie, V. A., Tran, A. M., Tollkuhn, J., et al. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2022.105203 · Cited by 27
Non-canonical G protein signaling
Nürnberg, B., Beer‐Hammer, S., Reisinger, E., & Leiss, V. (2024) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2024.108589 · Cited by 29
Short-chain fatty acids: key antiviral mediators of gut microbiota
Xu, Z., Wang, T., Wang, Y., Li, Y., Sun, Y., & Qiu, H. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1614879 · Cited by 37
Dix, A. V., Moss, S. M., Phan, K., Hoppe, T. A., Paoletta, S., Kozma, E., Gao, Z., Durell, S. R., Jacobson, K. A., & Appella, D. H. (2014) · Journal of the American Chemical Society · doi:10.1021/ja504288s · Cited by 27
Exploring Endocytosis and Intracellular Trafficking of the Human Serotonin1A Receptor
Kumar, G. A., Sarkar, P., Jafurulla, M., Singh, S. P., Srinivas, G., Pande, G., & Chattopadhyay, A. (2019) · Biochemistry · doi:10.1021/acs.biochem.9b00033 · Cited by 28
Artificial Intelligence and the detection of pediatric concussion using epigenomic analysis
Bahado-Singh, R. O., Vishweswaraiah, S., Er, A., Aydas, B., Türkoğlu, O., Taşkın, B. D., Duman, M., Yılmaz, D., & Radhakrishna, U. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146510 · Cited by 27
Lim, W. K., Chai, X., Ghosh, S., Ray, D., Wang, M., Rasheed, S. A. K., & Casey, P. J. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010018 · Cited by 27
“Heterotrimeric G proteins function as molecular switches; ligand binding to the GPCR triggers a conformational change in the transmembrane region of the receptor, resulting in a GDP– GTP exchange on the G subunit and its subsequent dissociation from the G dimer (6, 7).”
BackgroundRGS14 Regulation of Post-Synaptic Signaling and Spine Plasticity in Brain
Harbin, N. H., Bramlett, S. N., Montañez‐Miranda, C., Terzioğlu, G., & Hepler, J. R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136823 · Cited by 24
Monfared, R. V., Alhassen, W., Truong, T. M., Gonzales, M. A. M., Vachirakorntong, V., Chen, S., Baldi, P., Civelli, O., & Alachkar, A. (2021) · Cells · doi:10.3390/cells10112967 · Cited by 28
“, metabolism, proliferation, migration) and modulate cells’ interactions and responses to their environment, which implicate this superfamily in almost all physiological functions and pathological processes [2].”
BackgroundAbrol, R., Griffith, A. R., Bray, J. K., & Goddard, W. A. (2012) · Methods in molecular biology · doi:10.1007/978-1-62703-023-6_14 · Cited by 27
Oi, N., Suzuki, M., Terauchi, T., Tokunaga, M., Nakatani, Y., Yamamoto, N., Fukumura, T., Zhang, M., Suhara, T., & Higuchi, M. (2013) · Journal of Medicinal Chemistry · doi:10.1021/jm400772t · Cited by 27
Conservation of Molecular Interactions Stabilizing Bovine and Mouse Rhodopsin
Kawamura, S., Colozo, A. T., Müller, D. J., & Park, P. S. ‐. (2010) · Biochemistry · doi:10.1021/bi101345x · Cited by 29
Makita, N., Kabasawaa, Y., Otani, Y., Firman, Sato, J., Hashimoto, M., Nakaya, M., Nishihara, H., Nangaku, M., Kurose, H., et al. (2012) · Circulation Research · doi:10.1161/circresaha.112.277665 · Cited by 27
Alpha-carboxy nucleoside phosphonates as universal nucleoside triphosphate mimics
Balzarini, J. M., Das, K., Bernatchez, J. A., Martinez, S. E., Ngure, M., Keane, S., Ford, A., Maguire, N. M., Mullins, N., John, J., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1420233112 · Cited by 27
Green light to illuminate signal transduction events
Balla, T. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.08.001 · Cited by 27
Structural Determinants of Agonist-Selective Signaling at the sst2A Somatostatin Receptor
Nagel, F., Doll, C., Pöll, F., Kliewer, A., Schröder, H., & Schulz, S. (2011) · Molecular Endocrinology · doi:10.1210/me.2010-0407 · Cited by 27
Discovery of substituted benzamides as follicle stimulating hormone receptor allosteric modulators
Yu, H. N., Richardson, T. E., Nataraja, S. G., Fischer, D. J., Sriraman, V., Jiang, X., Bharathi, P., Foglesong, R. J., Haxell, T. F. N., Heasley, B. H., et al. (2014) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2014.03.018 · Cited by 27
Hoff, M., Balfanz, S., Ehling, P., Gensch, T., & Baumann, A. (2011) · The FASEB Journal · doi:10.1096/fj.11-180703 · Cited by 27
Andrews, S. P., & Tehan, B. G. (2012) · MedChemComm · doi:10.1039/c2md20164j · Cited by 27
Ceraudo, E., Hierso, R., Tan, Y., Murail, S., Rouyer‐Fessard, C., Nicole, P., Robert, J., Jamin, N., Neumann, J., Robberecht, P., et al. (2012) · The FASEB Journal · doi:10.1096/fj.11-196444 · Cited by 27
CCR5 Conformations Are Dynamic and Modulated by Localization, Trafficking and G Protein Association
Flegler, A. J., Cianci, G. C., & Hope, T. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089056 · Cited by 27
Extracellular acidification stimulates GPR68 mediated IL-8 production in human pancreatic β cells
Chandra, V., Karamitri, A., Richards, P., Cormier, F., Ramond, C., Jockers, R., Armanet, M., Albagli, O., & Scharfmann, R. (2016) · Scientific Reports · doi:10.1038/srep25765 · Cited by 27
Ancient and Recent Duplications Support Functional Diversity of Daphnia Opsins
Brandon, C. S., Greenwold, M. J., & Dudycha, J. L. (2016) · Journal of Molecular Evolution · doi:10.1007/s00239-016-9777-1 · Cited by 26
Lipid Rafts and Dopamine Receptor Signaling
Martinez, V. J., Asico, L. D., José, P. A., & Tiu, A. C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21238909 · Cited by 29
“The structure of GPCRs features the presence of seven transmembrane α-helical molecules, which are connected by three extracellular and three intracellular loops [10].”
BackgroundLiang, Q., He, J., Zhao, X., Xue, Y., Zuo, H., Ru, X., Jin, Y., Wang, J., Li, Q., & Zhao, X. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c00123 · Cited by 27
Grammatopoulos, D. K. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.02.013 · Cited by 26
Lysophosphatidylserine: A Signaling Lipid with Implications in Human Diseases
Chakraborty, A., & Kamat, S. S. (2024) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00701 · Cited by 24
Lan, W., Tang, Z., Liao, H., Chen, Q., Chen, Y. P., Zhang, Z., & Wang, J. (2025) · Fundamental Research · doi:10.1016/j.fmre.2025.01.004 · Cited by 28
“G protein-coupled receptors (GPCRs) are a large family of transmembrane proteins that play a crucial role in signal transduction across the cell membrane [ 75 ].”
Wichard, J., ter Laak, A., Krause, G., Heinrich, N., Kühne, R., & Kleinau, G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016811 · Cited by 26
Baltoumas, F. A., Theodoropoulou, M. C., & Hamodrakas, S. J. (2016) · Journal of Computer-Aided Molecular Design · doi:10.1007/s10822-016-9919-y · Cited by 26
Biased agonism and allosteric modulation of metabotropic glutamate receptor 5
Trinh, P. N. H., May, L. T., Leach, K., & Gregory, K. J. (2018) · Clinical Science · doi:10.1042/cs20180374 · Cited by 28
Opening up about Tissue Transglutaminase: When Conformation Matters More than Enzymatic Activity
Katt, W. P., Antonyak, M. A., & Cerione, R. A. (2018) · Med One · doi:10.20900/mo.20180011 · Cited by 24
Indiraleka, M., Rajendran, K., & Dhanaraj, P. (2020) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-020-03953-x · Cited by 26
Tutzauer, J., de Valdivia, E. G., Swärd, K., Eilard, I. A., Broselid, S., Kahn, R., Olde, B., & Leeb-Lundberg, L. M. F. (2021) · Molecular Pharmacology · doi:10.1124/molpharm.121.000259 · Cited by 26
A cholesterol analog stabilizes the human β 2 -adrenergic receptor nonlinearly with temperature
Serdiuk, T., Manna, M., Zhang, C., Mari, S. A., Kulig, W., Pluháčková, K., Kobilka, B. K., Vattulainen, I., & Müller, D. J. (2022) · Science Signaling · doi:10.1126/scisignal.abi7031 · Cited by 26
Self-citationNovel Cell Receptor System of Eukaryotes Formed by Previously Unknown Nucleic Acid-Based Receptors
Tetz, V., & Tetz, G. V. (2022) · Receptors · doi:10.3390/receptors1010003 · Cited by 23
Lee, S. H., Mak, A., & Verheijen, M. H. G. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1159756 · Cited by 26
“GPCRs are a large group of membranebound, metabotropic receptors, whose activation stimulates several cellular signaling pathways (Rosenbaum et al., 2009).”
BackgroundZvonok, N., Xu, W., Williams, J. S., Janero, D. R., Krishnan, S. C., & Makriyannis, A. (2010) · Journal of Proteome Research · doi:10.1021/pr900870p · Cited by 26
Suwa, M., Sugihara, M., & Ono, Y. (2011) · Pharmaceuticals · doi:10.3390/ph4040652 · Cited by 26
Cooperative, bottom‐up generation of rigid‐rod nanostructures through dynamic polymer chemistry
Folmer-Andersen, J. F., Buhler, E., Candau, S., Joulié, S., Schmutz, M., & Lehn, J. (2010) · Polymer International · doi:10.1002/pi.2864 · Cited by 26
Evidence that prokineticin receptor 2 exists as a dimer in vivo
Marsango, S., di Patti, M. C. B., Barra, D., & Miele, R. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0601-6 · Cited by 26
“GPCRs are classified into three main families according to the structure and length of their amino-terminus and the localization of the agonist-binding site [ 2 ].”
BackgroundHan, X., Tachado, S. D., Koziel, H., & Boisvert, W. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042765 · Cited by 27
Isin, B., Estiu, G. L., Wiest, O., & Oltvai, Z. N. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050186 · Cited by 27
What are they waiting for?—Tethered agonism in G protein-coupled receptors
Schöneberg, T., Kleinau, G., & Brüser, A. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.03.027 · Cited by 23
Jafurulla, M., Bandari, S., Pucadyil, T. J., & Chattopadhyay, A. (2016) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2016.10.016 · Cited by 26
Yu, R., Liu, H., Peng, X., Cui, Y., Song, S., Wang, L., Zhang, H., An, H., & Zhou, T. (2017) · Oncotarget · doi:10.18632/oncotarget.17449 · Cited by 26
Lemos, A., Melo, R., Preto, A. J., de Almeida, J. G., Moreira, I. S., & Cordeiro, M. N. D. S. (2018) · Current Neuropharmacology · doi:10.2174/1570159x16666180308161642 · Cited by 28
Massink, A., Amelia, T., Karamychev, A., & IJzerman, A. P. (2019) · Medicinal Research Reviews · doi:10.1002/med.21633 · Cited by 27
“K E YWORD S allosteric modulation, amiloride, drug discovery, G protein‐coupled receptors, 5‐(N,N‐hexamethylene)amiloride 1 | INTRODUCTION G protein‐coupled receptors (GPCRs) form a family of receptors with approximately 800 members that are responsible for many different physiological functions such as regulation of…”
BackgroundLarge‐Amplitude Conformational Changes in Self‐Assembled Multi‐Stranded Aromatic Sheets
Atcher, J., Mateus, P., Kauffmann, B., Rosu, F., Maurizot, V., & Huc, I. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202014670 · Cited by 26
Photoinduced receptor confinement drives ligand-independent GPCR signaling
Sánchez, M. F., Els‐Heindl, S., Beck‐Sickinger, A. G., Wieneke, R., & Tampé, R. (2021) · Science · doi:10.1126/science.abb7657 · Cited by 26
β-Arrestin-Dependent Deactivation of Mouse Melanopsin
Cameron, E. G., & Robinson, P. R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113138 · Cited by 28
Wang, H. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.0721307.x · Cited by 26
Structure–function relationship and physiological role of apelin and its G protein coupled receptor
Murali, S., & Aradhyam, G. K. (2023) · Biophysical Reviews · doi:10.1007/s12551-023-01044-x · Cited by 25
Zeng, C., Han, S., Pan, Y., Huang, Z., Zhang, B., & Zhang, B. (2024) · Clinical and Translational Medicine · doi:10.1002/ctm2.1592 · Cited by 25
“77 GPCRs activate G proteins, which are composed of α , β and γ sub-units, in turn transducing signals to downstream effectors.”
BackgroundDeng, F., Yang, R., Yang, Y., Li, X., Hou, J., Liu, Y., Lu, J., Huangfu, S., Meng, Y., Wu, S., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-06973-1 · Cited by 29
“As the main participant in signaling transduction in cell membrane, GPCR are responsible for most physiological responses caused by environmental stimuli in the body 71,72 .”
Gronenberg, W., Raikhelkar, A., Abshire, E., Stevens, J., Epstein, E., Loyola, K., Rauscher, M. J., & Buchmann, S. L. (2014) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.3089 · Cited by 25
G Protein–Coupled Receptors Revisited: Therapeutic Applications Inspired by Synthetic Biology
Heng, B. C., Aubel, D., & Fussenegger, M. (2013) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-011613-135921 · Cited by 26
Reprogramming G protein coupled receptor structure and function
Kéri, D., & Barth, P. (2018) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2018.07.008 · Cited by 27
“They are involved in a wide diversity of cellular and physiological processes, including immune responses, vision, neuronal communication and behavior(1).”
BackgroundSingle Proteoliposome High-Content Analysis Reveals Differences in the Homo-Oligomerization of GPCRs
Walsh, S. M., Mathiasen, S., Christensen, S. M., Fay, J. F., King, C., Provasi, D., Borrero, E. E., Rasmussen, S. G. F., Fung, J. J., Filizola, M., et al. (2018) · Biophysical Journal · doi:10.1016/j.bpj.2018.05.036 · Cited by 26
“Our data provide quantitative comparative insight into the oligomerization of three class A GPCRs: the b2-adrenergic receptor (b2AR), which binds adrenaline and noradrenaline in a variety of tissues to stimulate smooth muscle cell contraction (1); the cannabinoid receptor type 1 (CB1), which binds endocannabinoids in…”
BackgroundSelf-citationArtificial Signal Transduction across Membranes
Vanuytsel, S., Carniello, J., & Wallace, M. I. (2019) · ChemBioChem · doi:10.1002/cbic.201900254 · Cited by 26
Taneera, J., Mohammed, I., Mohammed, A. K., Hachim, M. Y., Dhaiban, S., Malek, A. I., Dunér, P., Elemam, N. M., Sulaiman, N. D., Hamad, M. A., et al. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.110592 · Cited by 24
Oncogene addiction to GNAS in GNASR201 mutant tumors
More, A., Ito, I., Haridas, V., Chowdhury, S., Gu, Y., Dickson, P. N., Fowlkes, N. W., & Shen, J. P. (2022) · Oncogene · doi:10.1038/s41388-022-02388-6 · Cited by 25
Zeghal, M., Laroche, G., Freitas, J. D., Wang, R., & Giguère, P. M. (2023) · Nature Communications · doi:10.1038/s41467-023-39132-x · Cited by 30
Role of Lipid-Mediated Effects in β2-Adrenergic Receptor Dimerization
Prasanna, X., Chattopadhyay, A., & Sengupta, D. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-11280-0_16 · Cited by 25
Mondal, S., Khelashvili, G., Johner, N. B., & Weinstein, H. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-7423-0_4 · Cited by 24
Neurotransmitter Receptor Localization: From Autoradiography to Imaging Mass Spectrometry
Manuel, I., Barreda‐Gómez, G., Román, E. G. D. S., Veloso, A., Fernández, J. A., Giralt, M. T., & Rodríguez‐Puertas, R. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500281t · Cited by 25
Xu, Q. Q., Chang, M. X., Sun, R., Xiao, F. S., & Nie, P. (2010) · BMC Immunology · doi:10.1186/1471-2172-11-25 · Cited by 25
Constitutively Active μ-Opioid Receptors
Connor, M. A., & Traynor, J. R. (2010) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-381298-8.00022-8 · Cited by 25
Janero, D. R., Lindsley, L., Vemuri, K. V., & Makriyannis, A. (2011) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2011.608063 · Cited by 25
Development of Fluorescent Ligands for the Human 5-HT1A Receptor
Alonso, D., Vázquez‐Villa, H., Gamo, A. M., Martínez-Esperón, M. F., Tortosa, M., Viso, A., de la Pradilla, R. F., Junquera, E., Aicart, E., Martín‐Fontecha, M., et al. (2010) · ACS Medicinal Chemistry Letters · doi:10.1021/ml100053y · Cited by 25
Uddin, M. S., Kim, H., Deyo, A., Naider, F. R., & Becker, J. M. (2012) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2011.647352 · Cited by 25
Singh, R. K., Ahalawat, N., & Murarka, R. K. (2015) · The Journal of Physical Chemistry B · doi:10.1021/jp509814n · Cited by 24
Relationships between Structural Dynamics and Functional Kinetics in Oligomeric Membrane Receptors
Edelstein, S. J., & Changeux, J. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.01.050 · Cited by 27
Putative cholesterol‐binding sites in human immunodeficiency virus (HIV) coreceptors CXCR4 and CCR5
Zhukovsky, M. A., Lee, P., Ott, A., & Helms, V. (2012) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.24211 · Cited by 25
Mechanism of GPCR-Directed Autoantibodies in Diseases
Ünal, H., Jagannathan, R., & Karnik, S. S. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-3381-1_13 · Cited by 25
What can simulations tell us about GPCRs
Sengupta, D., Joshi, M., Athale, C. A., & Chattopadhyay, A. (2015) · Methods in cell biology · doi:10.1016/bs.mcb.2015.11.007 · Cited by 24
Koufos, E., Chang, E. H., Rasti, E. S., Krueger, E. E., & Brown, A. C. (2016) · Biochemistry · doi:10.1021/acs.biochem.6b00430 · Cited by 25
Metadata
- Authors
- Rosenbaum, D. M., Rasmussen, S. G. F., & Kobilka, B. K.
- Affiliations
- Stanford Medicine (US)
- Venue
- Nature
- Published
- 2009-05
- Volume
- 459
- Issue
- 7245
- Pages
- 356-363
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3967846
- OpenAlex
- W1988097700
- Cited by
- 2,534
- References
- 73
- Citations by year
- 2026: 108 · 2025: 171 · 2024: 175 · 2023: 140 · 2022: 196 · 2021: 177 · 2020: 150 · 2019: 172 · 2018: 122 · 2017: 136 · 2016: 132 · 2015: 120 · 2014: 133 · 2013: 135 · 2012: 146
- FWCI
- 11.79
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Lundbeckfonden (R19-2008-2113)
- National Institute of General Medical Sciences (F32GM082028, R01GM083118)
- National Institute of Neurological Disorders and Stroke (R01NS28471, R01NS028471)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- G protein-coupled receptors, GPCR structure, GPCR activation, constitutive activity, membrane protein structure, therapeutic target, hormone signaling, neurotransmitter signaling
- MeSH terms
- Animals, Cytoplasm, Humans, Protein Conformation, Signal Transduction, Conserved Sequence, Receptors, G-Protein-Coupled, Opsins
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