Dr John A. G. Briggs
- Section Biochemistry and Biophysics
- Location Martinsried, Germany
- Election year 2025
Research
Research Priorities: Structural Biology, Viruses, Cryo-Electron Microscopy, Tomography, Membrane Trafficking, Cellular Protein Complexes
John A.G. Briggs is a biochemist. His research interests focus on virus structures and biologically relevant cellular protein complexes, which he investigates using advanced cryo-electron microscopy techniques. He studies the lifecycles of pathogenic enveloped viruses and cellular machineries that mediate intracellular vesicular transport. Besides cryo-electron microscopy he also advances tomography and image analysis methods to study trafficking vesicles and enveloped viruses within native environments.
Elucidating complex viral and cellular structures by means of electron microscopy and in particular advanced cryo-electron microscopy is the main goal of John A.G. Briggs, for which he contributed innovative and pioneering research. In this way, he was able to perform detailed analyses of the architecture of mature and immature particles of the human immunodeficiency virus (HIV) and related viruses. These studies provide insights into the mechanism of HIV particle assembly in the host cell and allow to draw conclusions about structural rearrangements during the process of viral maturation that are crucial for virus infectivity. Both processes are targets for new antiviral strategies. Other research by John A.G. Briggs focuses on the structure of other pathogenic viruses, e.g. the influenza virus and the Marburg virus.
Overall, the group is conducting research in three areas: Firstly, they are interested in the structure, assembly, and maturation of enveloped viruses, in particular HIV-1, influenza A virus and filoviruses. They study these processes using cryo-electron microscopy, tomography, biochemistry, and other complementary methods. Furthermore, the group use enveloped viruses as test systems for the development of data collection and image processing methods.
The second research area of the Briggs group focuses on coated vesicles transport material between the different compartments of the cell. They study how coated vesicles assemble, how they collect cargo, how they disassemble, and how these processes are regulated. To do this, they use “in situ” cryo-electron microscopy and tomography and reconstitute vesicle assembly using purified proteins and membranes in vitro.
John A.G. Briggs and his group work and perfect the fast-evolving cryo-electron microscopy and tomography techniques to find the location and spatial context of a protein complex at the same time as determining its structure, conformation and composition-within a single experiment. They work on the development of methods in the areas of sample preparation, data collection schemes, and image processing approaches for the analysis of big datasets. As model systems they use viruses and vesicles with properties convenient for testing and validating new methods.
John A.G. Briggs is a biochemist. His research interests focus on virus structures and biologically relevant cellular protein complexes, which he investigates using advanced cryo-electron microscopy techniques. He studies the lifecycles of pathogenic enveloped viruses and cellular machineries that mediate intracellular vesicular transport. Besides cryo-electron microscopy he also advances tomography and image analysis methods to study trafficking vesicles and enveloped viruses within native environments.
Elucidating complex viral and cellular structures by means of electron microscopy and in particular advanced cryo-electron microscopy is the main goal of John A.G. Briggs, for which he contributed innovative and pioneering research. In this way, he was able to perform detailed analyses of the architecture of mature and immature particles of the human immunodeficiency virus (HIV) and related viruses. These studies provide insights into the mechanism of HIV particle assembly in the host cell and allow to draw conclusions about structural rearrangements during the process of viral maturation that are crucial for virus infectivity. Both processes are targets for new antiviral strategies. Other research by John A.G. Briggs focuses on the structure of other pathogenic viruses, e.g. the influenza virus and the Marburg virus.
Overall, the group is conducting research in three areas: Firstly, they are interested in the structure, assembly, and maturation of enveloped viruses, in particular HIV-1, influenza A virus and filoviruses. They study these processes using cryo-electron microscopy, tomography, biochemistry, and other complementary methods. Furthermore, the group use enveloped viruses as test systems for the development of data collection and image processing methods.
The second research area of the Briggs group focuses on coated vesicles transport material between the different compartments of the cell. They study how coated vesicles assemble, how they collect cargo, how they disassemble, and how these processes are regulated. To do this, they use “in situ” cryo-electron microscopy and tomography and reconstitute vesicle assembly using purified proteins and membranes in vitro.
John A.G. Briggs and his group work and perfect the fast-evolving cryo-electron microscopy and tomography techniques to find the location and spatial context of a protein complex at the same time as determining its structure, conformation and composition-within a single experiment. They work on the development of methods in the areas of sample preparation, data collection schemes, and image processing approaches for the analysis of big datasets. As model systems they use viruses and vesicles with properties convenient for testing and validating new methods.
Career
- since 2021 Director, Department of Cell and Virus Structure, MPIB, Martinsried, Germany
- 2017-2021 Program Leader, Laboratory of Molecular Biology, Cambridge, Medical Research Council (MRC), UK
- 2017-2018 Group Leader, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany
- 2013-2018 Senior Scientist, EMBL, Heidelberg, Germany
- 2011-2016 Group Leader, Molecular Medicine Partnership Unit (MMPU), Medical Facultiy, University of Heidelberg, Heidelberg, EMBL, Heidelberg, Germany
- 2010-2016 Group Leader, Cell Biology and Biophysics Unit, EMBL, Heidelberg, Germany
- 2006-2016 Group Leader, Structural and Computational Biology Unit, EMBL, Heidelberg, Germany
- 2005-2006 Postdoctoral Research Fellow, Ludwig Maximilians University Munich, Munich, Germany
- 2004 Postdoctoral Scientist, University of Oxford, Oxford, UK
- 2000-2004 D.Phil. in Structural Biology, University of Oxford, Oxford, UK
- 1996-2000 Bachelor and Master in Natural Sciences (Biochemistry), University of Cambridge, Cambridge, UK
Projects
- since 2022 Head, Subproject “The role of matrix maturation in HIV-1 infection and spread”, Collaborative Research Centre (SFB) 1129, German Research Foundation (DFG), Germany
- 2014-2018 Head, Subproject “The assembly and spread of influenza Virus”, SFB 1129, DFG, Germany
- 2009-2012 Head, Subproject “Structure and arrangement of viral proteins in HIV, Marburg and Influenza viruses”, SFB 1175, DFG, Germany
- 2008-2015 Head, Subproject “Structural dynamics of coatomer”, SFB 638, DFG, Germany
- 2005-2011 Head, Project “Control and coherence of the few-particle continuum”, DFG, Germany
Honours and Memberships
- since 2025 Member, German National Academy of Sciences Leopoldina, Germany
- since 2025 Fellow, Royal Society, UK
- 2018 Finalist, UK Blavatnik Awards for Young Scientists, Blavatnik Family Foundation, New York City, USA
- 2015 Ernst Ruska Prize for outstanding achievements in electron microscopy, German Society for Electron Microscopy, Germany
- 2015 Member, European Molecular Biology Organization (EMBO)
- 2015 Award for Life Sciences, Royal Microscopical Society, UK
- 2012 Chica and Heinz Schaller Research Award, Chica and Heinz Schaller Foundation, Heidelberg, Germany
- 2005-2006 Long Term Fellowship, EMBO
- 2005 Research Fellowship, Alexander von Humboldt Foundation, Bonn, Germany