Bültmann & Gerriets
Structural Biology of the Complement System
von Dimitrios Morikis, John D. Lambris
Verlag: Taylor & Francis
E-Book / PDF
Kopierschutz: Adobe DRM


Speicherplatz: 16 MB
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ISBN: 978-0-8493-5036-8
Erschienen am 29.03.2005
Sprache: Englisch
Umfang: 370 Seiten

Preis: 80,49 €

Klappentext
Biografische Anmerkung
Inhaltsverzeichnis

The only in-depth guide on the subject, this is the first resource to present the structural biology of the complement system in connection to immunology and drug development. Integrating the latest breakthroughs in structural biology and immunology, this book includes detailed discussions of the structure-function relationships among complement system components, regulators, receptors, and selected proteins and inhibitor. It also provides an introduction to the structural bioinformatics classification of complement proteins. The book comes with a CD containing color figures, a molecular structure visualization program, and files with three-dimensional coordinates of the structures. OTI #1: 3150



Dimitrios Morikis received his B.S. in physics from Aristotle University of Thessaloniki, Greece, in 1983, and his M.S. and Ph.D. in physics from Northeastern University, Boston, in 1985 and 1990, respectively. He was trained in biophysics during his doctoral thesis work, in structural biology during his postdoctoral fellowship in 1990-1993 at the Department of Molecular Biology of The Scripps Research Institute, La Jolla, California, and in computational chemistry during a senior postdoctoral fellowship in 1999-2001 at the Department of Chemistry and Biochemistry of the University of California, San Diego. He is currently a member of the research faculty of the Department of Chemical and Environmental Engineering at the University of California, Riverside. He is also an adjunct associate professor at the Division of Immunology and the Department of Neurobiochemistry of the Beckman Research Institute of the City of Hope, Duarte, California. His research is highly cross-disciplinary, using experimental spectroscopic methods and theoretical computational methods. His current research focuses on immunophysics, structural bioinformatics, bioengineering, and biotechnology, including three-dimensional structure determination, the exploration of structure, dynamics, thermodynamics, and electrostatics of proteins and protein complexes of the immune system, rational drug design, and the design of peptides and small proteins with desired properties.

John D. Lambris received his Ph.D. in biochemistry in 1979. He is a professor in the Department of Pathology and Laboratory Medicine, and director of the Protein Chemistry Laboratory at the University of Pennsylvania, Philadelphia. Using complement as a model system, he applies ideas and methods embodied in engineering, computer science, physics, chemistry, biomedicine, and other fields to study the structure and functions of the complement system. His current research efforts focus on the structural-functional aspects of protein-protein interactions, and the rational design of small size-complement inhibitors. In addition, his research extends to the evolution and developmental aspects of the complement system as well as to viral molecular mimicry and immune evasion strategies.



The Building Blocks of the Complement System. Complement Control Protein Modules in Regulators of Complement Activation. The Classical Pathway to C1 Complex. Factors D and B: Substrate-Inducible Serine Proteases of the Alternative Pathway of Complement Activation. The Structures of Human Complement Fragments C3d and C4Ad and the Functional Insights that They Have Provided. Complement Receptor CR2/CD21 and CR2-C3d Complexes. Structure of the Anaphylatoxins C3a and C5a. C3b/C4b Binding Site of Complement Receptor Type 1 (CR1, CD35). From Structure to Function of a Complement Regulator: Decay-Accelerating Factor (CD55). Complement Protein C8. Structure-Function Relationships in CD59. Complement-Like Repeats in Proteins of the Complement System. Complement and Immunoglobulin Protein Structures by X-Ray and Neutron Solution Scattering and Analytical Ultracentrifugation. Structure, Dynamics, Activity, and Function of Compstatin and Design of More Potent Analogues. Discovery of Potent Cyclic Antagonists of Human C5a Receptors. Index.


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