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International School of Crystallography - Erice

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Ettore Majorana Foundation and Centre for Scientific Culture
President: Professor Antonino Zichichi


Director: Sir Tom Blundell, FRS FMedSci


Dear all,
given the current status of the COVID-19 pandemic, with great regret we decided to postpone this year's course until June 2023 (courses in Erice are scheduled and planned many years in advance; for this reason, we could not move the school to 2021 or even 2022).
It has not been an easy decision and, although we feel it is the right decision, we are very sorry for all the inconvenience that it may cause. We will reimburse anybody who has already paid the registration fee. If you are interested in participating in the 2023 school, guaranteed pre-registration will be available in July 2022. Check back on the website for further information. Please feel free to reach out to us with any questions.
Annalisa Guerri
Executive Secretary of the International School of Crystallography

55th Course:


Erice 29 May - 6 June 2020

Structural Drug Design 2020 Logo

Directors of the course:

G. Scapin

G. Scapin

MSD, Kenilworth, NJ, USA

C. Deane

C. Deane

Oxford University, UK

F. von Delft

F. von Delft

Diamond and Oxford University, UK

Apply now!

Note The result of the applications will be notified whithin the end of January


The past several years have produced transformations both in the long term management of chronic diseases and in the treatment of illnesses that previously seemed intractable. Nevertheless, understanding and managing human health remains one of the most challenging aspects of our society. One fundamental problem is the lack of a full comprehension of the underlying biology of healthy and diseased states. While structural information is still applied at different stages of the drug design process, especially during drug optimization, the focus has now decisively moved earlier, to providing tools for the understanding of the disease biology. This has resulted in traditional structural biology techniques being thoroughly integrated with other disciplines, including biophysics, informatics, biology and chemistry. Because of the continuously evolving experimental and computational techniques, the success of the entire process depends on proper management of the increasing complexity, diversity and volume of data generated. The purpose of the course is to provide the students with: a) an overview of the current structural and biophysical techniques used in the field; b) the use of informatics tools in drug discovery; c) the evolving role of chemistry in drug design and biology understanding; and d) an introduction to biologics and their applications.
Several case studies will be presented to highlight the different topics. Hands-on workshops and tutorials will complement the lectures.


click on the name to see bio-sketches

Rutgers University, Piscataway, NJ, USA

E. Arnold

Arnold Eddy Arnold, Board of Governors and Distinguished Professor of Chemistry and Chemical Biology at Rutgers University, works to understand the structural and molecular basis of the chemistry underlying life, with a focus on studying human disease problems and applying the insights gained to the development of better treatments. His research has profoundly influenced our understanding of the structure and biological function of viruses and their components, and his structure-guided efforts have yielded five therapeutic medicines for treating HIV/AIDS. The cross-disciplinary research in Arnold’s group uses a broad swath of tools and techniques from molecular biology, protein chemistry and biochemistry, biophysics, virology, crystallography, and cryo-EM. Eddy studied chemistry and organic chemistry at Cornell as an undergraduate and Ph.D. student. His postdoctoral work in Michael Rossmann’s laboratory culminated in elucidating the structure of a common cold virus (1985), the first animal virus described in complete atomic detail. His work has illuminated fundamental molecular mechanisms of viral polymerase structure and function, infection and escape from antiviral drugs and immune surveillance, and protein-nucleic acid and protein-ligand interactions. Eddy began his faculty career at Rutgers in 1987 with a focus on using crystallography to help discover drugs for treating HIV infection, which at the time was a death sentence. Eddy’s structure of HIV reverse transcriptase complexed with DNA (1993), the first polymerase visualized with a relevant substrate, changed the landscape of the HIV/AIDS and polymerase biochemistry fields. His longstanding collaboration with Stephen Hughes has resulted in extraordinarily diverse and innovative studies of HIV reverse transcriptase structure, function, inhibition, and resistance that have helped to make this critical enzyme the most thoroughly understood of any DNA polymerase. Arnold’s efforts with legendary drug developer Dr. Paul Janssen, enabled the design and discovery of five anti-AIDS drugs (etravirine, rilpivirine, Complera, Odefsey, and Juluca) that are broadly used for treating HIV-infected patients and are resilient to drug resistance. Arnold’s team developed the strategic flexibility hypothesis, which postulates that structural flexibility and compactness of inhibitors can overcome resistance mutations, a concept that can be applied to any disease target. His elegant analyses of RT drug inhibition and resistance mechanisms have likewise spawned generalizable principles. Crystallographic fragment screening efforts identified novel allosteric inhibitory sites in HIV-1 reverse transcriptase and led to new classes of antiviral inhibitors targeting influenza virus endonuclease and HIV-1 integrase. Publication list:


University of Florence, Florence, IT


Banci Lucia Banci is Professor of Chemistry at the University of Florence. She has an extensive expertise and has provided original contributions and breakthroughs in Structural Biology and in biological NMR. She has addressed and unraveled many aspects of the biology of metal ions in biological systems.
The innovative in cell NMR approach developed by Lucia Banci and her group allows for the detection of human individual proteins in living human cells with atomic level resolution. She also exploited the extensive knowledge of structural biology approaches through NMR expertise to develop an absolutely innovative approach to vaccine design, based on the knowledge of the structure of the pathogen antigens and of the interaction pattern with antibodies, to design structure-based vaccines.
Lucia Banci is one of the founders and former Director of the Center of Magnetic Resonance (CERM) of the University of Florence, which features an impressive battery of NMR spectrometers. She is the Head of the Italian Core Center of the ESFRI Research Infrastructure Instruct-ERIC, and a member of the Instruct-ERIC Executive Committee and of the Council.


Department of Biochemistry at Cambridge, UK

Sir Tom Blundell

Blundell Tom Blundell is Director of Research in the Department of Biochemistry, University of Cambridge, where he was previously Sir William Dunn Professor and Chair of School of Biological Sciences between 2003 and 2009. He has previously held positions in the Universities of London, Sussex and Oxford. Tom began his research career in Oxford, working with Nobel Laureate Dorothy Hodgkin on the first structure of a protein hormone, insulin. He has made major breakthroughs on the structural and computational biology and biophysics of hormones and growth factors (insulin, glucagon, NGF, HGF, FGF), receptor activation, signal transduction and DNA repair, important in cancer, tuberculosis and familial diseases. He has produced many widely used software packages for protein modelling and design, including Modeller (~10,500 citations) and Fugue (~1200 citations), and for predicting effects of mutations on protein stability and interactions (SDM & mCSM), to understand cancer & drug resistance. He has published ~630 research papers, including ~40 in Nature and Science, and has an H-factor of 114.
Tom has developed new approaches to structure-guided and fragment-based drug discovery. In 1999 he co-founded Astex Therapeutics, an oncology company that has eight drugs in clinical trials and that was sold in 2013 as Astex Pharma to Otsuka for $886 million. In parallel in the University of Cambridge he has developed structure-guided fragment-based approaches to drug discovery for difficult targets involving multiprotein systems and protein-protein interactions. He has also been targeting Mycobacterium tuberculosis proteins as part of the Gates HIT-TB consortia, M leprae for American Leprosy Mission and M. abscessus for Cystic Fibrosis Trust, including structural and biochemical studies of resistance mutations to first-line drugs.
Tom was a member of PM Margaret Thatcher’s Advisory Council on Science & Technology (1988-1990), Founding CEO of Biotechnology and Biological Sciences Research Council, 1991-1996 (Chair 2009-2015), Chairman, Royal Commission on Environment (1998-2005), Deputy Chair of Institute of Cancer Research 2008-2015 and President of UK Science Council, 2011- 2016.


Exscientia, Oxford, UK

A. Bradley

Bradley Dr. Bradley is multi-disciplinary scientist in computer-aided compound design using structural data. He completed a first-class MChem in Chemistry from the University of Oxford in 2010. He carried out an interdisciplinary DPhil also at the University of Oxford on the SABS-IDC programme. During this he developed computational tools (OOMMPPAA and WONKA) for structure-based drug design - lead by the SGC Oxford (Brian Marsden) and GlaxoSmithKline (Ian Wall and Darren Green) and the University of Oxford (Charlotte Deane).
Subsequent to his DPhil he carried out a post-doc at the RCSB PDB (UC San Diego) where he worked on novel compression algorithms for macromolecules, including the MMTF file format ( He then worked as a Project Leader between the Oxford Chemistry department, Diamond Light Source and the SGC Oxford on the XChem project (High-throughput X-ray screening of fragments). Here he generated tools ( and future funding for fragment-based compound optimisation leveraging the XChem platform. Since October 2018 he has worked at Exscientia, as Head of Design Sciences, where he leverages Exscientia’s Centaur Platform for compound design and develops novel methods that will further improve the platform.


Heptares, Cambridge, UK

M. Congreve

Congreve Miles Congreve is Senior Vice President, Head of Drug Discovery at Sosei Heptares (Cambridge, UK) and has responsibility for creating the company’s pipeline of GPCR-targeted agents. He previously held senior medicinal chemistry positions at Astex Therapeutics and GSK. A recognised expert in structure and fragment-based drug design, he has participated in the discovery of several agents that have progressed to at least phase 2 clinical trials (to date) including AZD4635, Vofopitant, Lanabecestat, Onalespib, and Capivasertib. He is co-inventor of Ribociclib (Kisqali®) which received FDA approval as first-line treatment for HR+/HER2- metastatic breast cancer in combination with any aromatase inhibitor in March 2017 and contributed to discovery of Erdafitinib (Balversa®) which was approved by the FDA in April 2019 for treatment of locally advanced or metastatic bladder cancer. He has co-authored ~100 publications and is co-inventor of over 50 patents. His work in the area of FBDD has been highly influential, helping to establish and show the importance of the approach, including proposing the ‘Rule of 3’ for fragments. He was co-recipient of the Royal Society of Chemistry Malcolm Campbell Memorial Prize 2015 for his role in the seminal contributions to GPCR drug discovery made by Heptares.


Vernalis, Cambridge, UK

B. Davis

Davis Dr Ben Davis is a Research Fellow at Vernalis Research, a biotech company based in Cambridge UK which has been at the forefront of fragment-based approaches since 1998. An NMR spectroscopist and biophysicist by training, his research focus is developing and applying NMR and other biophysical techniques to enable drug discovery against challenging therapeutic targets and systems.
Dr Davis studied for his PhD in protein folding and ligand binding with Professor Alan Fersht at Cambridge University, and then studied small molecule interactions with a range of biomolecules by NMR. He has over 25 years’ experience of NMR and biophysics in the drug discovery industry. He has contributed to six books over the last decade and is an author on more than thirty scientific publications. He is a frequent speaker at scientific conferences and has been running FBLD and NMR training workshops since 2007.


St. Jude Children's Research Hospital, Memphis, TN

M. Fischer

Fischer Marcus Fischer discovered his passion for structural biology during his undergraduate studies in the beautiful Hanseatic city of Lübeck (Germany). During his B.Sc. & M.Sc. studies he conducted research projects in Montpellier (France), Shanghai (China), and Toronto (Canada). He received a Ph.D. in Structural Biology and Chemistry from the University of York (UK) where he worked with Rod Hubbard on fragment-based ligand discovery. During his postdoc with Brian Shoichet in San Francisco (USA), he traded fog for glacial winter temperatures during a “sabbatical” year in Toronto. It remains unconfirmed whether the Toronto winter made him question cryogenic practices in crystallography. His postdoctoral work used model proteins to isolate important terms for computational ligand discovery, especially protein flexibility and solvation. In July 2017 he joined the faculty of St. Jude Children’s Research Hospital as an Assistant Professor. Combining an interest in chemical and structural biology, his lab is exploiting protein conformational landscapes for ligand discovery in pediatric cancer.


Weizmann Institute of Science, Rehovot, IL

S.J. Fleishman

Fleishman Dr. Sarel Fleishman is an assistant professor at the Weizmann Institute of Science, where his research team develops computational protein-design methodology to address challenges in biochemistry and protein engineering. As a postdoc with David Baker in Seattle (2007-2011), Sarel developed the first accurate methods for designing protein binders, culminating in the design of broad-specificity influenza inhibitors. At the Weizmann Institute (2011-), his team developed protein design methods to the level of accuracy and reliability required to design large and complex proteins such as enzymes, antibodies, and vaccine immunogens. The team recently developed a fully automated method, called PROSS, for dramatically improving the stability and expressibility of recalcitrant proteins and several design methods for improving affinity, specificity, and catalytic rates in antibodies and enzymes. Current focuses include developing methods for designing large repertoires comprising millions of enzymes or antibodies for one-shot isolation of highly active, specific, and stable binders, inhibitors, or enzymes. Among Sarel’s academic awards were the Clore Ph.D. Fellowship (2003-2006), the ScienceMagazine award for a young molecular biologist (2008), a postdoctoral fellowship (2006-2009) and a career-development award (2012-2015) from the Human Frontier Science Program, European Research Council Starting and Consolidator Grants (ongoing), the Alon Fellowship, the Henri Gutwirth Prize, and the Weizmann Scientific Council Award.


UCSF, San Francisco, CA, USA

J. Fraser

Fraser James Fraser was an undergraduate at McGill University in Montreal, Canada. He moved to California in 2005 for his PhD in Molecular and Cellular Biology at UC Berkeley. There, he worked with Tom Alber creating biophysical methods to characterize protein side chain flexibility in high resolution X-ray electron density maps to reveal the structural basis for critical functional motions in enzymes. Near the end of his PhD, he was an EMBO Visiting Short-Term Fellow in Dan Tawfik’s lab at the Weizmann Institute in Israel. Concurrently, he authored the problems and solutions manual for the physical chemistry textbook The Molecules of Life by John Kuriyan, Boyana Konforti, and David Wemmer. In 2011, James started his independent career as a UCSF. He is currently an Associate Professor in the Dept. of Bioengineering and Therapeutic Sciences. He is also a Consulting Professor in Photon Science at the Stanford SLAC National Laboratory and a Faculty Scientist at Lawrence Berkeley National Lab. The long-term goals of his lab's research program are to understand how protein conformational ensembles are reshaped by perturbations and to quantify how these perturbations impact protein function and organismal fitness. James is a recipient of the NIH Early Independence Award, a Pew Scholar Award, a Searle Scholar Award, and a Packard Fellowship. He is an ardent supporter of open science and publishing practices, primarily through the preprint advocacy group ASAPbio.


Novartis, Basel, CH

S. Jacob

Jacob Sandra Jacob is executive director and head of Protein Sciences in the Chemical Biology and Therapeutics department of the Novartis Institutes for BioMedical Research in Basel, Switzerland. Her group works mainly in hit/lead discovery and optimization doing protein production of soluble and membrane proteins and using X-ray, EM, NMR and other biophysical methods to find and characterize interactions of ligands with proteins and RNA. Sandra is recognized for her expertise in kinase inhibition and her work has resulted in the discovery of Tasigna, a drug for the treatment of Chronic Myelogenous Leukemia. She is a driver of novel approaches for target modulation, the most recent examples being non-ATP site inhibitors of kinases. She studied Chemistry at the University of Melbourne in Australia and followed this up with a Ph.D. using protein crystallography at the St. Vincent’s Institute of Medical research in Melbourne. She joined Ciba Geigy, now Novartis, after studies including lipocalins at Uppsala University in Sweden and focusing on membrane proteins at the University of Basel..

Marburg University, Marburg, DE


G. Klebe

Klebe Focus of our research is directed toward the understanding of protein-ligand interactions, including chemical synthesis, microcalorimetry, molecular biology, crystallography, bioinformatics and software development. Internationally recognized software tools such as CoMSIA, AFMoC, DrugScore, Relibase/Cavbase or MOBILE have been developed in our laboratory. Several drug discovery projects concentrate on the discovery of leads for neglected and poverty-related disease targets. To obtain better insight into affinity and selectivity determining features fundamental research is performed on serine and aspartyl proteases, aldose/aldehyde reductase and several kinases and hydrolases. Gerhard Klebe studied chemistry at the University of Frankfurt/M, Germany, and obtained his doctorate in physical chemistry. After postdoctoral positions in crystallography (Grenoble, CNRS and ILL, France, and Univ. of Berne, Switzerland) he was responsible for molecular modeling and crystallography at BASF-AG in Ludwigshafen, Germany. In 1996 he moved to Philipps-University of Marburg, Germany, to take a professorship in Pharmaceutical Chemistry. In 2005 he refused an offer from ETH Zürich, for a chair in Pharmaceutical Chemistry, serves on the editorial board of several journals, was member of the Board of Governors of the CCDC and the advisory board of the Leibniz-Institute FMP in Berlin. He has written a text book on Drug Design which appeared either in the German and English language. In 2011 the research of his group was awarded an ERC Advanced Grant by the European Research Council on the "Chemogenomic profiling of drug-protein binding by shape, enthalpy/entropy and interaction kinetics" with particular emphasis to understand the influence of water on ligand binding. Presently, his groups installs together with scientists at Bessy, HZB Berlin, a crystallography-based fragment screening beamline facility. From his group more than 370 scientific papers and more than 1000 PDB entries have emerged. He organized in two years frequency an International Workshop on New Approaches in Drug Discovery and Design and work a textbook on drug design.

MSD, Boston, MA, USA


C. Lesburg

Lesburg Charles Lesburg received his A.B. in Chemistry from Harvard College in 1991, and a Ph.D. in Biological Chemistry from the University of Pennsylvania in 1997, having trained in the laboratory of Prof. David W. Christianson. There he studied structure-function relationships in mutants of carbonic anhydrase II in collaboration with the laboratory of Prof. Carol Fierke and also kicked off a fruitful collaboration with the laboratory of Prof. David Cane studying sesquiterpene synthases. Employed at the Schering-Plough Research Institute in Kenilworth NJ, he published the first structure of the RNA-dependent RNA polymerase from hepatitis C virus, and subsequently contributed to a series of drug discovery programs as well as structural studies of pregnane X receptor, a common off-target metabolic liability for drug progression. After the acquisition by Merck & Co., he moved in 2013 to the Merck Research Laboratories site in Boston MA to enhance the drug discovery efforts with local structural expertise and has been involved in many programs – mainly concerning oncology and immunology – including identification and optimization of small molecule inhibitors and agonists, as well as peptides and oligonucleotides. He remains passionate about the development and use of computational tools for the organization and dissemination of macromolecular structural information, from experiment to analysis. Since 2005, Dr. Lesburg has served on the board (and as Chair from 2007 to 2009) of the Industrial Macromolecular Crystallographic Association, a consortium dedicated to the funding and operation of synchrotron X-ray beamlines to support its membership.

Vertex, Boston, MA, USA


G. McGaughey

McGaughey Georgia McGaughey is the Senior Director of the global Modeling & Informatics group at Vertex Pharmaceuticals Inc., comprised of molecular modeling, informatics and methods development. Through her twenty-year career in pharmaceuticals (Wyeth, Merck, Vertex) Georgia has contributed to the invention and advancement of several clinical candidates and marketed medicines (e.g. BACE, orexin, PDE10, CFTR and KDR) and has contributed to more than 100 publications and presentations. She is a past member of the editorial advisory board for the Journal of Medicinal Chemistry and participant of multiple study sections for the NIH. Currently, she volunteers in the Boston scientific community through mentorship with high school and college students, is an editorial board member of the Journal of Chemical Information and Modeling, serves on Silent Spring Institute’s board and is a member of the Scientific Advisory Board for the Cambridge Crystallographic Data Centre (CCDC). Georgia earned her B.S. degree in chemistry from Kennesaw State College and her Ph.D in physical chemistry from the University of Georgia. She carried out her post-doctoral studies with focus on electronic structure theory at Colorado State University. She is also an avid runner and plays the piano.

Lonza, Manchester, UK


O. Obrezanova


AstraZeneca, Goeteborg, SE


J. Petersen

Petersen Dr. Jens Petersen is an Associate Principal Scientist and structural biologist From Astrazeneca in Gothenburg. He graduated from the University of Copenhagen where he was involved in establishing the first group in X-ray crystallography and carried out structural studies on plant peroxidases. He did his postdoc with Prof Michael N.G. James at the University of Alberta where he carried out studies on viral proteases and protease inhibitors. Since 1999 he has been working within the Structure, Biophysics and Fragments department in Astrazeneca in Gothenburg. He is an expert within structural biology and structure based drug design with specific target class expertise within nuclear hormone receptors, proteases and lipid kinases. He has co-authored more than 30 papers, patents, posters and presentations.

ETH, Zurich, CH


S. Riniker

Riniker Sereina Riniker completed her Master’s degree in chemistry at ETH Zurich in 2008. After an internship in the research department of Givaudan AG and a research stay at the University of California Berkeley, she returned in 2009 to ETH Zurich to obtain a PhD in molecular dynamics simulations. From 2012 to 2014, she held a postdoctoral position in cheminformatics at the Novartis Institutes for BioMedical Research in Basel and Cambridge, Massachusetts.
Since June 2014, Sereina Riniker is an Assistant Professor (with tenure track) of Computational Chemistry at the Department of Chemistry and Applied Biosciences at ETH Zurich.

UCSF, San Francisco, CA, USA


J. Taunton

Taunton Jack Taunton obtained his Ph.D. in chemistry from Harvard University. As a graduate student, Jack identified and cloned histone deacetylase (HDAC1) as the molecular target of trapoxin, a fungal natural product.
After postdoctoral studies at Harvard Medical School, Jack joined the faculty of the University of California, San Francisco, where he is currently a Professor in the Department of Cellular and Molecular Pharmacology.
His research focuses on structure-based design of covalent inhibitors and chemoproteomic probes, as well as mechanistic studies of cyclic peptide natural products.

Chapman University, CA, USA


G. Verkhivker

Wade Dr. Verkhivker is currently Professor of Computational Biosciences at Schmid College of Science & Technology, Chapman University and Professor at the Department of Biomedical and Pharmaceutical Sciences at Chapman University School of Pharmacy. He is also Adjunct Professor of Pharmacology at the Department of Pharmacology, and Skaggs School of Pharmacy and Pharmaceutical Sciences, UC San Diego. Dr. Verkhivker received his PhD in Physical Chemistry from Moscow State University and completed a postdoctoral fellowship in computational biophysics from University of Illinois at Chicago. In his industrial career, Dr. Verkhivker played a leading role in establishing one of the first structure-based drug design technology platforms and building the largest computational group in pharmaceutical industry at Agouron Pharmaceuticals and Pfizer. He has been Director of Structural Bioinformatics and Structure-Based Drug Design at Pfizer Global Research and Development, La Jolla Laboratories. Dr. Verkhivker has led computational biology and structure-based drug design groups at Pfizer in discovering the first FDA-approved personalized cancer agent Xalkori. Since 2002, he has been Adjunct Professor of Pharmacology at the Skaggs School of Pharmacy and Pharmaceutical Sciences, UC San Diego. In 2006 he joined School of Pharmacy and Center for Bioinformatics at The University of Kansas as a Full Professor of Pharmaceutical Chemistry and Bioinformatics. In 2011 Dr. Verkhivker assumed position of Full Professor of Computational Biosciences at Schmid College of Science & Technology and Professor of Biomedical and Pharmaceutical Sciences at Chapman University School of Pharmacy in Irvine, CA. He is a founding member of the Structural Biology Center at the Chapman University School of Pharmacy and member of Chao Family Comprehensive Cancer Center , University of California Irvine. Dr. Verkhivker authored more than 150 peer reviewed publications and is recognized for his research contributions in the fields of bioinformatics, computational biophysics, computational biology and drug discovery. His most recent research activities are in the areas of computational systems biology, translational bioinformatics, network science and artificial intelligence with the focus on application of these approaches in translational cancer research. His research groups are involved in multidisciplinary studies that combine structural and computational biology with machine learning and artificial intelligence technologies to dissect molecular mechanisms and develop novel strategies for discovery of allosteric modulators of therapeutically important families of protein kinases and molecular chaperones. The innovative computational approaches developed by Prof. Verkhivker and his group allow for rational engineering of novel functions and design of selective kinase inhibitors. He is an Associated Editor of International Journal of Molecular Sciences and Frontiers in Molecular Biosciences, and a member of Advisory Boards of several biotech companies.

HITS and Heidelberg University, DE


R. Wade

Wade Rebecca Wade leads the Molecular and Cellular Modeling group at Heidelberg Institute for Theoretical Studies (HITS) and is Professor of Computational Structural Biology at the Center for Molecular Biology at Heidelberg University (ZMBH). Rebecca Wade studied at Oxford University and, following postdoctoral research at the universities of Houston and Illinois, became a group leader at the European Molecular Biology Laboratory (EMBL) in Heidelberg in 1992. She moved to HITS in 2001. Rebecca Wade’s research is focused on the development and application of computer-aided methods to model and simulate biomolecular interactions. Her research group has developed novel protein structure-based methods for drug discovery and protein engineering, most recently for studying drug binding kinetics, as well as multiresolution computational approaches to investigate macromolecular association and the effects of macromolecular crowding. Rebecca Wade’s research has been published in over 250 scientific papers, as well as software programs and web servers that are used world-wide. She is an Associate Editor of the Journal of Molecular Recognition and PloS Computational Biology. She was the recipient of the 2004 Hansch Award of the QSAR and Modelling Society and the 2016 International Society of Quantum Biology and Pharmacology (ISQBP) Award in Computational Biology. URL:

City of Hope, Duarte, CA, USA


J. Williams

Williams John Williams is a Professor of Molecular Medicine and the co-Director of the Drug Discovery and Structural Biology program at Beckman Research Instittue at City of Hope. His thesis work, application of solid state NMR to study protein dynamics, was conducted at Columbia University under the supervision of Professor Ann McDermott. He studied X-ray diffraction at EMBL Heidelberg as an Alexander von Humboldt scholar under the direction of Rik Wierenga. He continued his postdoctoral studies at Columbia Presbyterian Medical College under the supervision of Professor Wayne Hendrickson. He applied structural and biophysical methods to understand the regulation of the dynein motor complex (while an Asst. Professor at Thomas Jefferson University) before relocating to City of Hope. Currently, his lab uses structural methods to design and functionalize antibodies and biologics. These efforts also involve the application of diffraction methods to discover small molecules to improve affinity thorough avidity and/or regulate activity. The result of these efforts have led to multiple, pending and issued patents and two spin out biotech companies. Finally, as a co-director of the Drug Discovery and Structural Biology program, Dr. Williams and his team are deeply involved in obtaining structure information as part of an institution wide medicinal chemistry effort.

Previous Schools

2019 • 54th Course
Cryo 3D Electron Microscopy
Directors: Dorit Hanein · Steven Ludtke · Stefan Raunser

2019 • 53rd Course
Magnetic Crystallography
Directors: Branton J. Campbell · Maria Teresa Fernandez-Diaz · J. Manuel Perez-Mato

2018 • 52nd Course
Quantum Crystallography
Directors: Dylan Jayatilaka · Piero Macchi

2018 • 51st Course
Electron Crystallography
Directors: Joke Hadermann · Lukas Palatinus · Andy Stewart

Future Schools

2021 • 56th Course
Molecular Crystal Engineering

2022 • 57th Course
High Pressure Crystallography

2022 • 58th Course
Diffuse Scattering

2023 • 59th Course
Structural Biology

2024 • 60th Course
Powder Diffraction

Giovanna Scapin

Scapin Giovanna Scapin graduated Magna cum Laude in 1985 from Padova University (Italy) with a degree in Organic Chemistry. In 1989 she received her PhD in Organic Chemistry from the same university with a thesis in Structural Biology. In February 1990 Giovanna joined the laboratory of Dr. James C. Sacchettini at the Albert Einstein College of Medicine, Bronx (NY), as postdoctoral fellow, and subsequently as Instructor. Her interest was initially for a class of small fatty acid binding proteins that had been related to obesity and diabetes. Subsequently most of her work was involved in bacterial enzymes that could be used as target for the design of novel antibiotics. During the 6 years Giovanna spent there, she mentored several graduated students and post-doctoral fellows.
In 1997 Giovanna joined Merck and Co., Inc, where she was involved in several drug discovery projects, providing structural biology support for diabetes, inflammation and oncology targets. Her more recent work focused on the diabetes target DPP-4, on novel antimicrobial targets, and on the structure-function of antibodies. After spending 18 month as embedded scientist at the New York Structural Biology Center – Simons Electron Microscopy Center to learn hands-on single particle CryoEM, since the spring of 2018 Giovanna is back full time at Merck, where she established a new cryoEM facility.
Publication list: here
LinkedIn profile: here

Charlotte Deane

Deane Charlotte Deane is Professor of Structural Bioinformatics in the Department of Statistics at the University of Oxford. She did her undergraduate degree at University College, Oxford and received her PhD from the University of Cambridge. She then moved to UCLA on a Wellcome Trust Research Fellowship and took up a group leader position in Oxford in 2002. Since then she has set up and directed an MSc programme as well as two Centres for Doctoral Training. She is currently the director of the Sustainable Approaches to Biomedical Sciences Centre for Doctoral training. This is an open innovation EPSRC/MRC and industry funded centre, with over twenty partner companies.
Charlotte also leads the Oxford Protein Informatics group, a research group of over 20 people working on diverse problems across protein structure, immunoinformatics, interaction networks and small molecule drug discovery. Her work combines both theoretical and empirical analysis with special interests in artificial intelligence. This involves close collaborations with experimentalists in both academia and industry in the design of experiments to leverage the power of computation for biological insight.
Her work focusses on the development of novel algorithms, tools and databases all of which are openly available to the community. Examples include SAbDab, SAbPred, PanDDA and MEMOIR. These tools are widely used web resources (SAbDab alone has over 500 unique users a month) and are also part of several Pharma drug discovery pipelines, including GSK, Roche, Medimmune, Kymab, Iontas, Lonza and UCB.

Frank Von Delft

Delft Frank von Delft is Professor of Structural Chemical Biology at the University of Oxford, where he heads the Protein Crystallography group of the Structural Genomics Consortium; and Principal Beamline Scientist at Diamond Light Source, head of the I04-1 experimental station and the associated XChem programme for fragment screening. He is also Visiting Professor at the Department of Biochemistry at the University of Johannesburg. After studying biochemistry, chemistry and applied mathematics in Bloemfontein, South Africa, he completed his PhD in crystallography at Cambridge under Tom Blundell, followed by postdoctoral work in high-throughput crystallography at the JCSG in San Diego at the Scripps Institute, as well as Syrrx, Inc.
As structural biologist, he is seeking to reshape how protein structure determination transforms rational drug design, by developing and making the new methodologies and tools available through platforms and products to ensure they are widely and routinely used by researchers world-wide. His long-term programme is to shrink by two orders of magnitude the time and cost required to develop small molecule inhibitors, by combining national facilities, artificial intelligence, robotics and cloud-based open access science, in order to make the bespoke design of inhibitors a consistently cheap, fast and widely-used approach in biology and medicine.
He leads three research facilities that serve large user communities, are critical to multiple large, international research networks, and provide the outlet for wide-spread use of my methodologies. At Oxford for the Structural Genomics Consortium (SGC), he run the crystallography infrastructure that serves 100s of researchers. At Diamond Light Source, beamline I04-1 is used by at least 100 crystallography groups annually, and the world-first XChem facility seeds 30 academic and industrial drug discovery experiments annually with high-quality data. He has authored or co-authored over 100 publications, and he is co-applicant on several large international initiatives totalling over £70m.