

Anastassis Perrakis
Netherlands Cancer Institute
<p>Dr. Anastassis Perrakis is a Group Leader in Structural Biology in the Division of Biochemistry at the Netherlands Cancer Institute and Professor of “Macromolecular Structures” in Utrecht University. His team has a strong background in developing computational and laboratory methods for macromolecular X-ray crystallography, allowing to determine macromolecular structures efficiently and accurately. His biological research on protein structure-function relationships, focuses on two themes: deciphering the signalling axis established by the autotaxin (ATX) extracellular phospholipase that produced the signalling lipid LPA which has numerous physiological roles and therapeutic applications; and analysing the biochemical basis of dynamic microtubule interactions and modifications in regulating mitotic progression and other cellular functions. For this research, his group is using biochemical and biophysical approaches, including various X-ray methods, cryo-EM, NMR and other spectroscopic approaches. In parallel he is an investigator in the Oncode Institute aiming to understand cancer for translating research into practice, and in particular utilise fragment based lead discovery approaches for the development of new drug leads. Finally, he is the coordinator of the iNEXT-Discovery Horizon2020 project to enable access to structural biology research infrastructures for all European researchers, and especially to non-experts in structural biology.</p>

Hans Wienk
Netherlands Cancer Institute
<p>Dr. Hans Wienk is a Project Manager in the Division of Biochemistry at the Netherlands Cancer Institute (NKI) in Amsterdam. He has a PhD in membrane biophysics from Utrecht University (2000), and postdoctoral training in Nuclear Magnetic Resonance at the Goethe University. Before iNEXT he was a post-doctoral fellow and then Facility Manager of the NMR spectroscopy group at the Utrecht University Bijvoet Centre, the largest NMR facilities in Europe; he is an expert in protein spectral assignments, structure calculations, interactions and dynamics. Since 2015 he has been managing the European Commission Horizon2020 project “iNEXT”. He has prepared and is now managing the follow-up “iNEXT-Discovery” Horizon2020 project. Both projects combine over twenty well-established European research groups and facilities for structural biology (NMR, X-rays, Electron Microscopy, Biophysics), that together offer coordinated facility access to hundreds of users, technical and scientific training, as well as networking and dissemination activities to stimulate structural biology research for health, food and biotechnology.</p>
Integrative structural biology uses a large variety of biophysical methods that provide detailed knowledge of the atomic and molecular structure of macromolecules, isolated or in their native environment. This provides a better understanding of the basic of chemistry of life and helps with the development of new biotechnology tools, drugs, and biomaterials. Access to large-scale installations (synchrotrons producing X-rays, state-of-the-art electron microscopes, powerful NMR magnets) is necessary for research in structural biology. This Methods Collection will describe the most important methods for the structural analysis of macromolecules, applications in fragment-based lead drug discovery, methods to investigate the structure of macromolecules in their native environment, and high throughput approaches for structural determination. It will consist of a variety of methods that includes, but is not limited to, NMR, cryo-EM, X-ray crystallography, and scattering.
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Hans Wienk1, Lucia Banci2, Susan Daenke3, Eva Pereiro4, Harald Schwalbe5, David Ian Stuart6, Manfred S. Weiss7, Anastassis Perrakis1
1Division of Biochemistry and Oncode Institute, The Netherlands Cancer Institute, Amsterdam, 2CERM/CIRMMP, University of Florence, 3Instruct-ERIC, Oxford University, 4MISTRAL beamline, Alba Light Source, 5Center for Biomolecular Magnetic Resonance (BMRZ), Goethe University Frankfurt, 6Division of Structural Biology, Oxford University, 7Macromolecular Crystallographyy, Helmholtz-Zentrum Berlin
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Jan Wollenhaupt1, Tatjana Barthel1,2, Gustavo M. A. Lima3, Alexander Metz4, Dirk Wallacher5, Elmir Jagudin3, Franziska U. Huschmann1,4, Thomas Hauß1, Christian G. Feiler1, Martin Gerlach1, Michael Hellmig1, Ronald Förster1, Michael Steffien1, Andreas Heine4, Gerhard Klebe4, Uwe Mueller1, Manfred S. Weiss1
1Macromolecular Crystallography, Helmholtz-Zentrum Berlin, 2Structural Biochemistry Group, Institute for Chemistry and Biochemistry, Freie Universität Berlin, 3BioMAX, MAX IV Laboratory, 4Drug Design Group, Institute of Pharmaceutical Chemistry, Philipps-Universität Marburg, 5Department Sample Environment, Helmholtz-Zentrum Berlin
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Cited by 8
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A. Jiménez-Moreno1, L. del Caño1, M. Martínez1, E. Ramírez-Aportela1, A. Cuervo1, R. Melero1, R. Sánchez-García1, D. Strelak1,2,3, E. Fernández-Giménez1, F.P. de Isidro-Gómez1, D. Herreros1, P. Conesa1, Y. Fonseca1, D. Maluenda1, J. Jiménez de la Morena1, J.R. Macías1, P. Losana1, R. Marabini1, J.M. Carazo1, C.O.S. Sorzano1,4
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Alice Douangamath*1,2, Ailsa Powell*1,2, Daren Fearon*1,2, Patrick M. Collins1,2, Romain Talon1,2,3, Tobias Krojer3,4, Rachael Skyner1,2, Jose Brandao-Neto1,2, Louise Dunnett1,2, Alexandre Dias1,2, Anthony Aimon1,2,3, Nicholas M. Pearce1,3, Conor Wild3,5, Tyler Gorrie-Stone1, Frank von Delft1,2,3,4,6
1Diamond Light Source Ltd, Harwell Science and Innovation Campus, 2Research Complex at Harwell, Harwell Science and Innovation Campus, 3Structural Genomics Consortium, University of Oxford, 4Centre for Medicines Discovery, University of Oxford, 5Oxford Protein Informatics Group, Department of Statistics, Oxford University, 6Department of Biochemistry, University of Johannesburg
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Sam Horrell1, Danny Axford1, Nicholas E. Devenish1, Ali Ebrahim1, Michael A. Hough2, Darren A. Sherrell1,3, Selina L. S. Storm1,4, Ivo Tews5, Jonathan A. R. Worrall2, Robin L. Owen1
1Diamond Light Source, Harwell Science and Innovation Campus, 2School of Life Sciences, University of Essex, 3X-ray Science Division, Argonne National Laboratory, 4European Molecular Biology Laboratory, Hamburg Outstation c/o DESY, 5Biological Sciences, Institute for Life Sciences, University of Southampton
crystallisation and high throughput room temperature data collection from protein crystals at beamline VMXi
Mike Hough*1
1Diamond light source