NMR of Biomolecules

Ivano Bertini is a Professor of Chemistry and Founding Director of the Magnetic Resonance Center (CERM) at the University of Florence. His main research interests include advancements in nuclear magnetic resonance spectroscopy, the expression and preparation of metalloproteins, their structural characterization, and the investigation of their interactions, with an emphasis on understanding cellular processes at the molecular level. He has authored over 600 scientific publications and several books, and is or has been on the editorial staff or advisory board of over 20 of the most authoritative journals in chemistry, biochemistry and inorganic chemistry. He is a member of the Academia Europaea and the Italian Accademia dei Lincei. Kathleen S. McGreevy is a researcher in bioinformatics at the Magnetic Resonance Center (CERM) at the University of Florence. After obtaining a degree in Mechanical Engineering from the University of Virginia in 2002, she became involved in the support and management of research activities in the biomedical sciences before moving to her current position. She has been involved in the management of several European projects, notably the FP6-funded Coordination Action NMR-Life, from which this volume takes its inspiration. Giacomo Parigi, degree in Physics at the University of Florence (1992) and PhD in Chemistry, is Associate Professor of General and Inorganic Chemistry at the Magnetic Resonance Center (CERM) and the Department of Chemistry of the University of Florence. His research interests are mainly oriented to the study of NMR effects related to paramagnetism for the structural and dynamic characterization of biomolecules, to the analysis of the relaxometric profiles of paramagnetic systems and biomolecules, and to nuclear and electron relaxation.

Website: www.wiley-vch.de/home/nmrbiomol INTRODUCTION NMR and its place in Mechanistic Systems Biology (Bertini, McGreevy, Parigi) The structure of biomolecules: fundamentals Structural features of proteins (Banci, Cantini) Structural features of nucleic acids (Cevec, Jonker, Nozinovic, Richter, Schwalbe) What can be learned about the structure and dynamics of biomolecules from NMR Proteins studied by NMR (Ferella, Rosato, Turano) Nucleic acids studied by NMR (Plavec) THE ROLE OF NMR IN THE STUDY OF THE STRUCTURE AND DYNAMICS OF BIOMOLECULES Determination of protein structure and dynamics (Ferella, Rosato, Turano) DNA (Plavec) RNA (Stefl, Sklenr) Intrinsically disordered proteins (Felli, Pierattelli, Tompa) Paramagnetic molecules (Bertini, Luchinat, Parigi) THE ROLE OF NMR IN THE STUDY OF THE STRUCTURE AND DYNAMICS OF BIOMOLECULAR INTERACTIONS NMR methodologies for the analysis of protein interactions (Madl, Sattler) Metal-mediated interactions (Ciofi-Baffoni) Protein-paramagnetic protein interactions (Keizers, Hiruma, Ubbink) Protein-RNA interactions (Manoharan, Perez-Canadillas, Ramos) Protein-DNA interactions (Kovacic, Boelens) NMR IN DRUG DISCOVERY High-throughput screening and fragment-based design: general considerations for lead discovery and optimization (Pellecchia) Ligand-observed NMR in fragment-based approaches (Sledz, Abell, Ciulli) Interactions of metallodrugs with DNA (Sadler) RNA as a drug target (Ferner, Duchardt-Ferner, Rinnenthal, Buck, Whnert, Schwalbe) Fluorine NMR spectroscopy for biochemical screening in drug discovery (Dalvit) NMR of peptides (Beck, Frank, Kessler) SOLID-STATE NMR Biomolecular solid state NMR - basics (Barbet-Massin, Pintacuda) Protein dynamics in the solid-state (Lewandowski, Emsley) Microcrystalline proteins - An ideal benchmark for methodology development (Franks, van Rossum, Bardiaux, Ravera, Parigi, Luchinat, Oschkinat) Structural studies of protein fibrils by solid-state NMR (Bckmann, Meier) Membrane proteins (Cukkemane, Renault, Baldus) FRONTIERS IN NMR SPECTROSCOPY Dynamic nuclear polarization (Prisner) 13C direct detection NMR (Felli, Pierattelli) Speeding up multidimensional NMR data acquisition (Brutscher, Marion, Frydman) Metabolomics (Tenori) In cell NMR spectroscopy (Burz, Cowburn, Dutta, Shekhtman) Structural investigation of cell-free expressed membrane proteins (Sobhanifar, Reckel, Lhr, Bernhard, Dtsch) COMPUTATIONAL ASPECTS Grid computing (Rosato) Protein-protein docking with HADDOCK (Schmitz, Melquiond, de Vries, Karaca, van Dijk, Kastritis, Bonvin) Automated protein structure determination methods (Guerry, Herrmann) NMR structure determination of protein-ligand complexes (Schieborr, Sreeramulu, Schwalbe) SAXS/SANS as methods complementary to NMR (Petoukhov, Svergun)