Stamou Group

The Stamou Group studies membranes and membrane proteins at the nanoscale using fluorescence microscopy, with research spanning membrane curvature, single-molecule transport, GPCRs and nanoscopic heterogeneity.

Research focus

Bionanotechnology and Nanomedicine

Our lab is developing disruptive technologies to study the physico-chemical properties of membranes and membrane proteins on the nanoscale using fluorescence microscopy. Membrane proteins are one of the most important classes of proteins in biology comprising more than 60% of existing pharmaceutical targets.

Biological membranes enable the function of membrane proteins and therefore play a key role themselves in governing a plethora of biological processes. Our work provides a path towards new generations of therapeutic agents based on entirely new biological principles and is thus frequently done in collaboration with world-leading industrial partners including Aquaporin, Chr.Hansen, Novozymes and Novo Nordisk.

Group leader

Research area

Our lab is developing disruptive technologies to study membranes and membrane proteins on the nanoscale using fluorescence microscopy. Membrane proteins are one of the most important classes of proteins in biology comprising more than 60% of existing pharmaceutical targets. Our current work focuses on two ubiquitous families of transmembrane proteins, G protein coupled receptors and transporters.

The exciting problems we are investigating are situated at the interface of biology, physics and nanotechnology, and to address them experimentally we have assembled a dynamic, interdisciplinary, group of top-tier biophysicists, biochemists, molecular and cellular biologists, and nanotechnologists.

In a breakthrough paper in Science [1] we developed a method that resolved ionic currents with a million-fold higher sensitivity than the Nobel prize awarded method of patch clamp (atto-amperes).

This allowed us to observe for the first time the function of single transporters, revealing the existence of functional heterogeneity based on hitherto unknown off-cycle states (i.e. ultra-stable inactive and leaky states with lifetimes 105-fold longer than those of states in the classical transport cycle).

The dramatic consequence of this unforeseen complexity is that many fundamental mechanistic tenets that were based on macroscopic experiments of transport will have to be revised.

This truly transformative innovation is the crowing achievement of a decade of research in our lab[2,3] and we believe is likely to spark off a technological and conceptual paradigm shift in the transport field.

Eukaryotic life is defined by the existence of intracellular membrane-bound organelles.

Endomembranes are overall more curved than the plasma membrane their heterogeneous geometrical shapes however are not arbitrary, on the contrary they are so characteristic that they have become a hallmark of the different eukaryotic organelles.[4]

To elucidate why this phenotype is so remarkably conserved we have pioneered several high-throughput nanoscopic methods to study how membrane curvature is affecting the function(s) of membranes and membrane proteins, with an emphasis on Ras and G protein coupled receptors.[5-7]

Our contributions have overall helped establish the notion that the properties of biological membranes are defined equally by their lipid composition and their geometrical shape.[4]

Spatiotemporal compositional and functional heterogeneities are a hallmark of biological membranes. We are investigating the implications of these heterogeneities for biological function and also exploit them for technological applications.

For example, with high-throughput single proteoliposome measurements we quantified the composition of single proteoliposomes revealing dramatic heterogeneities.[8]

As we showed, compositional heterogeneities can severely skew ensemble-average proteoliposome measurements however, if averaging is avoided such heterogeneities can be exploited to enable high-content screens that enable a dramatic reduction in protein consumption (~billion-fold) as compared to conventional assays.[8]

We are currently extending this project to investigate nanoscopic compositional and functional heterogeneities of G protein coupled receptors in live cells.

References

  • Science, 2016. 351 (6280): p. 1469-1473        
    Direct observation of proton pumping by a eukaryotic P-type ATPase 
    Salome Veshaguri, Sune M. Christensen, Gerdi C. Kemmer, Mads P. Møller, Garima Ghale, Christina Lohr, Andreas L.Christensen, Bo H. Justesen, Ida L. Jørgensen, Jürgen Schiller, Nikos S. Hatzakis, Michael Grabe, Thomas Günther Pomorski, Dimitrios Stamou                  
  • Proceedings of the National Academy of Sciences. 2009. 106 (30): p. 12341
    Quantification of nano-scale intermembrane contact areas using fluorescence resonance energy transfer.                 
    Poul Martin Bendix, M. S. Pedersen and Dimitrios Stamou.
  • Nature Nanotechnology, 2012. 7 (1): p. 51–55                   
    Mixing sub-attolitre volumes in a quantitative and highly parallel manner with soft matter nanofluidics.
    S. M. Christensen; P.Y. Bolinger; N.S. Hatzakis; M.W. Mortensen and Dimitrios Stamou
  • Nature Chemical Biology, 2015. 11 (11): p. 822-825          
    Membrane curvature bends the laws of physics and chemistry
    Lars Iversen, Signe Mathiasen, Jannik Bruun Larsen, Dimitrios Stamou
  • Nature Chemical Biology, 2009. 5 (11): p. 835                   
    How Curved Membranes Recognize Amphipathic Helices and Protein Anchoring Motifs.
    N. S. Hatzakis, V. K. Bhatia, J. Larsen, K. L. Madsen, P. Y. Bolinger, A. H. Kunding, J. Castillo, U. Gether, P. Hedegård and Dimitrios Stamou.
  • Nature Chemical Biology, 2015. 11 (3): p. 192-194            
    Front Cover Page 
    Membrane curvature enables N-Ras lipid anchor sorting to liquid-ordered membrane phases
    Jannik Bruun Larsen, Martin Borch Jensen, Vikram K. Bhatia, Søren L. Pedersen, Thomas Bjørnholm, Lars Iversen, Mark Uline, Igal Szleifer, Knud J. Jensen, Nikos S. Hatzakis and Dimitrios Stamou
  • Nature Chemical Biology, 2017. 13: p. 724-729.
    Front Cover Page
    Membrane curvature regulates sorting of GPCRs within the plasma membrane of living cells in a ligand-specific manner
    Kadla R. Rosholm, Natascha Leijnse, Anna Mantsiou, Vadym Tkach, Søren L. Pedersen, Volker F. Wirth, Lene B. Oddershede, Knud J. Jensen, Karen L. Martinez, Nikos S. Hatzakis, Poul Martin Bendix, Andrew Callan-Jones and Dimitrios Stamou
  • Nature Methods, 2014. 11 (9): p. 931-934     
    Nanoscale high content analysis using compositional heterogeneities of single proteoliposomes
    Signe Mathiasen, Sune M. Christensen,, Juan Jose Fung, Soren G. F. Rasmussen, Jonathan F. Fay, Sune K. Joergensen, Salome Veshaguri, David L. Farrens, Maria Byrne, Brian Kobilka, Dimitrios Stamou

Research keywords

  • Nanoscale membrane biophysics
  • Membrane curvature
  • Single molecules
  • Fluorescence microscopy
  • Ras
  • G protein coupled receptors
  • Primary and secondary active transporters.

Projects

We love what we do. If you also feel driven by scientific curiosity, join us! Our dynamic, interdisciplinary team will introduce you to truly cutting-edge science.

Our projects will typically involve state of the art fluorescence microscopes to image either living cells or proteins reconstituted in vesicles. We typically analyse our images in Matlab.

You will be studying the most important targets for the pharmaceutical industry: G protein coupled receptors or transporters.

Selected publications

  • Science, 2016. 351 (6280): p. 1469-1473 Full text
    Direct observation of proton pumping by a eukaryotic P-type ATPase. S. Veshaguri, S. M. Christensen, G. C. Kemmer, M. P. Møller, G. Ghale, C. Lohr, A. L.Christensen, B. H. Justesen, I. L. Jørgensen, J. Schiller, N. S. Hatzakis, M. Grabe, T. G. Pomorski and D. Stamou
  • Nature Chemical Biology, 2015. 11 (11): p. 822-825 Full text
    Invited Review Commentary for celebrating the 10th anniversary of Nature Chemical Biology Membrane curvature bends the laws of physics and chemistry. L. Iversen, S. Mathiasen, J. B. Larsen and D. Stamou
  • Nature Chemical Biology, 2015. 11 (3): p. 192-194 (Front cover page) Full text
    Membrane curvature enables N-Ras lipid anchor sorting to liquid-ordered membrane phases. J.B. Larsen, M.B. Jensen, V.K. Bhatia, S.L. Pedersen, T. Bjørnholm, L. Iversen, M. Uline, I. Szleifer, K.J. Jensen, N.S. Hatzakis and D. Stamou
  • Nature Methods, 2014. 11 (9): p. 931-934 Full text
    Nanoscale high content analysis using compositional heterogeneities of single proteoliposomes. S. Mathiasen, S.M. Christensen,, J.J. Fung, S.G.F. Rasmussen, J.F. Fay, S.K. Joergensen, S. Veshaguri, D.L. Farrens, M. Byrne, B. Kobilka and D. Stamou
  • Science, 2014. 345 (6192): p. 50-54 Full text
    Single molecule analysis of Ras activation by SOS reveals allosteric regulation via altered fluctuation dynamics. L. Iversen, H.-L. Tu, W.-C. Lin, S. M. Christensen, S. M. Abel, J. Iwig, H.-J. Wu, J. Gureasko, C. Rhodes, R. S. Petit, S. D. Hansen, P. Thill, C.-H. Yu, D. Stamou, A. K. Chakraborty, J. Kuriyan and J. T. Groves.
  • Nature Nanotechnology, 2012, 7 (1): p. 51–55 Full text
    Mixing sub-attolitre volumes in a quantitative and highly parallel manner with soft matter nanofluidics. S.M. Christensen, P.Y. Bolinger, N.S. Hatzakis, M.W. Mortensen and D. Stamou
  • Nature Chemical Biology, 2009. 5 (11): p. 835 Full text
    How Curved Membranes Recognize Amphipathic Helices and Protein Anchoring Motifs. N.S. Hatzakis, V.K. Bhatia, J. Larsen, K.L. Madsen, P.Y. Bolinger, A.H. Kunding, J. Castillo, U. Gether, P. Hedegård and D. Stamou
  • Proceedings of the National Academy of Sciences, 2009. 106 (30): p. 12341 Full text
    Quantification of nano-scale intermembrane contact areas using fluorescence resonance energy transfer. P.M. Bendix, M.S. Pedersen and D. Stamou

Current group members

Name
Title
Contact info

Contact

Dimitrios Stamou
Professor
  • Job responsibility
    Head of group