David E. Gloriam

David E. Gloriam


David Gloriam started his research career at Uppsala University where he in 2006 received a PhD degree for the bioinformatic discovery of 24 human receptors and the overall receptor repertoires in dog, mouse, rat and chicken. In 2006-7, he was at the European Molecular Biology Laboratory (EMBL) – Bioinformatics Institute where he developed a global protein informatics standard and data exchange format for protein affinity reagents. In 2007-2008, he made another postdoc at GlaxoSmithKline where he conducted computational drug design and developed chemogenomic methods for ligand/drug discovery. Since late 2008, he has been at the Department of Drug Design and Pharmacology at the University of Copenhagen where he has expanded his research to scientific database development, data science and experimental structural biology. In 2019, he became the leader of a Departmental Cluster for GPCR Function and Drug Discovery and in 2020 he also became affiliated with a Faculty Center for Health Data Science.

He has been awarded Lundbeck Foundation Fellow (2014), ERC Starting Grantee (2015), Novo Nordisk Foundation Hallas-Møller Ascending Investigator (2018) and Lundbeck Foundation Ascending Investigator (2019). In 2013, he won a global structure modelling competition, GPCR Dock (best apo serotonin 5-HT1B receptor model). In 2013, he was appointed the new leader of his field’s main database, GPCRdb.org, which has evolved to an indispensable research infrastructure serving 4,000 multidisciplinary scientists each month. In 2017, the Chemical & Engineering News magazine of the American Chemical Society looked back on the past decade of GPCR research featuring GPCRdb along with his landmark publication on receptor drugs, targets and disease indications in Nat Rev Drug Discov (>530 citations in first 2,5 years). In 2019, he received a full Professorship in Computational Receptor Biology through a rare and exclusive personal calling and was selected for the UCPH Forward Talent Program at the University of Copenhagen.

Research direction
I consolidate my research on G protein-coupled receptors (GPCRs) – which mediate the effects of 1/3rd (ref) of drugs and 2/3rd of hormones (ref). My group develops computational and data driven methods for interdisciplinary receptor research and drug discovery, spanning:

  • Biased signalling towards safer drugs and specific signalling probes: Mechanisms and resources to design drugs with higher potency and fewer side effects by steering the receptor signalling onto only beneficial cellular pathways.
  • Computational drug design: Identification of druggable molecules for disease-relevant receptors and tool compounds to characterise understudied ‘orphan’ receptors or dissect GPCR signalling pathways.
  • Data science approaches to uncover receptor function: Discovery of physiological peptide hormones and determinants of receptor activation, effector G protein selectivity, genetic variants etc.
  • Experimental structural biology: Development of protein engineering tools combined with an in-house laboratory to determine drug-receptor structure complexes.
  • Online research infrastructure: GPCRdb resources integrating sequence-structure-function to offer reference data, analysis/visualisation, experiment design and data deposition upon publication.

Read more at the web sites of the Gloriam group and the Cluster for GPCR Function and Drug Discovery.

See Web of Science (requires subscription), Scopus and Google scholar.


Udvalgte publikationer

  1. Udgivet

    Combinatorial expression of GPCR isoforms affects signalling and drug responses

    Marti-Solano, M., Crilly, S. E., Malinverni, D., Munk, Christian, Harris, M., Pearce, A., Quon, T., Mackenzie, A. E., Wang, X., Peng, J., Tobin, A. B., Ladds, G., Milligan, G., Gloriam, David E., Puthenveedu, M. A. & Babu, M. M., 2020, I: Nature. 587, s. 650-656 28 s.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  2. Udgivet

    Discovery of Human Signaling Systems: Pairing Peptides to G Protein-Coupled Receptors

    Foster, S. R., Hauser, Alexander Sebastian, Vedel, L., Strachan, R. T., Huang, X., Gavin, A. C., Shah, S. D., Nayak, A. P., Haugaard-Kedström, L. M., Penn, R. B., Roth, B. L., Bräuner-Osborne, Hans & Gloriam, David E., 31 okt. 2019, I: Cell. 179, 4, s. 895-908

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  3. Udgivet

    An online resource for GPCR structure determination and analysis

    Munk, Christian, Mutt, E., Isberg, V., Nikolajsen, L. F., Bibbe, J. M., Flock, T., Hanson, M. A., Stevens, R. C., Deupi, X. & Gloriam, David E., 2019, I: Nature Methods. 16, 2, s. 151-162

    Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

  4. Udgivet

    GPCRdb in 2018: adding GPCR structure models and ligands

    Pándy-Szekeres, G., Munk, Christian, Tsonkov, T. M., Mordalski, S., Harpsøe, Kasper, Hauser, Alexander Sebastian, Bojarski, A. J. & Gloriam, David E., 2018, I: Nucleic Acids Research. 46, D1, 7 s., gkx1109.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  5. Udgivet

    Trends in GPCR drug discovery: new agents, targets and indications

    Hauser, Alexander Sebastian, Gloriam, David E., Attwood, M. M., Rask-Andersen, M. & Schiöth, H. B., 27 okt. 2017, I: Nature Reviews. Drug Discovery. 16, s. 829-842 14 s., 178.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  6. Udgivet

    GPCRmd uncovers the dynamics of the 3D-GPCRome

    Rodríguez-Espigares, I., Torrens-Fontanals, M., Tiemann, J. K. S., Aranda-García, D., Ramírez-Anguita, J. M., Stepniewski, T. M., Worp, N., Varela-Rial, A., Morales-Pastor, A., Medel-Lacruz, B., Pándy-Szekeres, G., Mayol, E., Giorgino, T., Carlsson, J., Deupi, X., Filipek, S., Filizola, M., Gómez-Tamayo, J. C., Gonzalez, A., Gutiérrez-de-Terán, H., Jiménez-Rosés, M., Jespers, W., Kapla, J., Khelashvili, G., Kolb, P., Latek, D., Marti-Solano, M., Matricon, P., Matsoukas, M., Miszta, P., Olivella, M., Perez-Benito, L., Provasi, D., Ríos, S., Torrecillas, I. R., Sallander, J., Sztyler, A., Vasile, S., Weinstein, H., Zachariae, U., Hildebrand, P. W., De Fabritiis, G., Sanz, F., Gloriam, David E., Cordomi, A., Guixà-González, R. & Selent, J., 2020, I: Nature Methods. 17, 8, s. 777-787

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  7. Udgivet

    Pharmacogenomics of GPCR Drug Targets

    Hauser, Alexander Sebastian, Chavali, S., Masuho, I., Jahn, L., Martemyanov, K., Gloriam, David E. & Babu, M., jan. 2018, I: Cell. 172, s. 41–54

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  8. Udgivet

    5-HT2C Receptor Structures Reveal the Structural Basis of GPCR Polypharmacology

    Peng, Y., McCorvy, J. D., Harpsøe, Kasper, Lansu, K., Yuan, S., Popov, P., Qu, L., Pu, M., Che, T., Nikolajsen, L. F., Huang, X., Wu, Y., Shen, L., Bjørn-Yoshimoto, Walden, Ding, K., Wacker, D., Han, G. W., Cheng, J., Katritch, V., Jensen, Anders A., Hanson, M. A., Zhao, S., Gloriam, David E., Roth, B. L., Stevens, R. C. & Liu, Z., 2018, I: Cell. 172, 4, s. 719-730 P719-730.E14.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

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