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Author: Steve Chao-Chung Shih Publisher: ISBN: Category : Languages : en Pages : 0
Book Description
Structure determination of membrane proteins by solution nuclear magnetic resonance spectroscopy require that they can be incorporated into detergent micelles in order to ensure that they are maintained in a folded, water-soluble state. However, detergent molecules produce micelle-protein complexes that pose unique challenges for solution NMR studies. To improve the spectroscopic properties of these complexes, it is possible to use specific isotope labeling strategies developed for the study of large water-soluble proteins by solution NMR. Specifically, the use of a highly deuterated sample that retains protons only in the Val, Leu and Ile (delta1) methyl groups has the potential to be used to determine structures of polytopic helical membrane proteins. However, while the quality of structure that can be obtained from this approach has been examined for water-soluble proteins, its utility for this class of membrane proteins has not been systematically investigated. This thesis evaluates the utility of this method for structure determination of membrane proteins by exploring structure calculation strategies from simulated NMR data sets from membrane proteins of known structure. Here I present results for a set of membrane proteins that consist of pairs or bundles of hydrophobic alpha-helices. I analyzed the impact of intra- and inter-helical NOEs on structure quality for samples specifically labeled with protons only at the methyl and amide positions In addition, I also explored the role of dihedral angles and residual dipolar couplings in an effort to find general trends to improve the accuracy of structures for polytopic a-helical membrane proteins. Based on the results of these calculations it appears that obtaining a uniform distribution of inter-helical NOES and accurately identifying transmembrane helices for dihedral angle restraints are the most important factors determining the accuracy of these simulated membrane protein structures. These results should help to guide future structure determinations for polytopic alpha-helical membrane proteins of unknown structure.
Author: Steve Chao-Chung Shih Publisher: ISBN: Category : Languages : en Pages : 0
Book Description
Structure determination of membrane proteins by solution nuclear magnetic resonance spectroscopy require that they can be incorporated into detergent micelles in order to ensure that they are maintained in a folded, water-soluble state. However, detergent molecules produce micelle-protein complexes that pose unique challenges for solution NMR studies. To improve the spectroscopic properties of these complexes, it is possible to use specific isotope labeling strategies developed for the study of large water-soluble proteins by solution NMR. Specifically, the use of a highly deuterated sample that retains protons only in the Val, Leu and Ile (delta1) methyl groups has the potential to be used to determine structures of polytopic helical membrane proteins. However, while the quality of structure that can be obtained from this approach has been examined for water-soluble proteins, its utility for this class of membrane proteins has not been systematically investigated. This thesis evaluates the utility of this method for structure determination of membrane proteins by exploring structure calculation strategies from simulated NMR data sets from membrane proteins of known structure. Here I present results for a set of membrane proteins that consist of pairs or bundles of hydrophobic alpha-helices. I analyzed the impact of intra- and inter-helical NOEs on structure quality for samples specifically labeled with protons only at the methyl and amide positions In addition, I also explored the role of dihedral angles and residual dipolar couplings in an effort to find general trends to improve the accuracy of structures for polytopic a-helical membrane proteins. Based on the results of these calculations it appears that obtaining a uniform distribution of inter-helical NOES and accurately identifying transmembrane helices for dihedral angle restraints are the most important factors determining the accuracy of these simulated membrane protein structures. These results should help to guide future structure determinations for polytopic alpha-helical membrane proteins of unknown structure.
Author: Jean-Jacques Lacapère Publisher: Methods in Molecular Biology ISBN: Category : Science Languages : en Pages : 482
Book Description
Membrane proteins, representing nearly 40% of all proteins, are key components of cells involved in many cellular processes, yet only a small number of their structures have been determined. Membrane Protein Structure Determination: Methods and Protocols presents many detailed techniques for membrane protein structure determination used today by bringing together contributions from top experts in the field. Divided into five convenient sections, the book covers various strategies to purify membrane proteins, approaches to get three dimensional crystals and solve the structure by x-ray diffraction, possibilities to gain structural information for a membrane protein using electron microscopy observations, recent advances in nuclear magnetic resonance (NMR), and molecular modelling strategies that can be used either to get membrane protein structures or to move from atomic structure to a dynamic understanding of a molecular functioning mechanism. Written in the highly successful Methods in Molecular BiologyTM series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Comprehensive and easy to use, Membrane Protein Structure Determination: Methods and Protocols serves as an ideal reference for scientists seeking to further our knowledge of these vital and versatile proteins as well as our overall understanding of the complicated world of cell biology.
Author: Isabel Moraes Publisher: Springer ISBN: 3319350722 Category : Science Languages : en Pages : 188
Book Description
This book reviews current techniques used in membrane protein structural biology, with a strong focus on practical issues. The study of membrane protein structures not only provides a basic understanding of life at the molecular level but also helps in the rational and targeted design of new drugs with reduced side effects. Today, about 60% of the commercially available drugs target membrane proteins and it is estimated that nearly 30% of proteins encoded in the human genome are membrane proteins. In recent years much effort has been put towards innovative developments to overcome the numerous obstacles associated with the structure determination of membrane proteins. This book reviews a variety of recent techniques that are essential to any modern researcher in the field of membrane protein structural biology. The topics that are discussed are not commonly found in textbooks. The scope of this book includes: Expression screening using fluorescent proteins The use of detergents in membrane protein research The use of NMR Synchrotron developments in membrane protein structural biology Visualisation and X-ray data collection of microcrystals X-ray diffraction data analysis from multiple crystals Serial millisecond crystallography Serial femtosecond crystallography Membrane protein structures in drug discovery The information provided in this book should be of interest to anyone working in the area of structural biology. Students will find carefully prepared overviews of basic ideas and advanced protein scientists will find the level of detail required to apply the material directly to their day to day work. Chapters 4, 5, 6, 8 and 9 of this book are published open access under a CC BY 4.0 license at link.springer.com.
Author: Hartmut Michel Publisher: CRC Press ISBN: 1351088173 Category : Medical Languages : en Pages : 343
Book Description
The precise knowledge of the structure of biological macromolecules forms the basis of understanding their function and their mechanism of action. It also lays the foundation for rational protein and drug design. The only method to obtain this knowledge is still crystallography. At present, the structures of about 400 proteins are known at or nearly at atomic proteins. However, only two of them are membrane proteins or complexes of the membrane proteins. The reasons for the difference is not the crystals of membrane proteins resists forming special problems when being analysed. The reason is that the membrane proteins resist into forming into well-ordered crystals. The intention of this book is to help to produce well-ordered crystals proteins and to provide guidelines, it is aimed at both biochemists and protein crystallographer‘s.
Author: Publisher: Academic Press ISBN: 0080961592 Category : Science Languages : en Pages : 334
Book Description
This volume of Current Topics in Membranes focuses on Membrane Protein Crystallization, beginning with a review of past successes and general trends, then further discussing challenges of mebranes protein crystallization, cell free production of membrane proteins and novel lipids for membrane protein crystallization. This publication also includes tools to enchance membrane protein crystallization, technique advancements, and crystallization strategies used for photosystem I and its complexes, establishing Membrane Protein Crystallization as a needed, practical reference for researchers.
Author: Christophe Chipot Publisher: Springer Science & Business Media ISBN: 3540384472 Category : Language Arts & Disciplines Languages : en Pages : 528
Book Description
Free energy constitutes the most important thermodynamic quantity to understand how chemical species recognize each other, associate or react. Examples of problems in which knowledge of the underlying free energy behaviour is required, include conformational equilibria and molecular association, partitioning between immiscible liquids, receptor-drug interaction, protein-protein and protein-DNA association, and protein stability. This volume sets out to present a coherent and comprehensive account of the concepts that underlie different approaches devised for the determination of free energies. The reader will gain the necessary insight into the theoretical and computational foundations of the subject and will be presented with relevant applications from molecular-level modelling and simulations of chemical and biological systems. Both formally accurate and approximate methods are covered using both classical and quantum mechanical descriptions. A central theme of the book is that the wide variety of free energy calculation techniques available today can be understood as different implementations of a few basic principles. The book is aimed at a broad readership of graduate students and researchers having a background in chemistry, physics, engineering and physical biology.
Author: Steve Chao-Chung Shih
Author: Steve Chao-Chung Shih
Author: Steve Chao-Chung Shih
Author: Michael Farah Mesleh
Author: Jean-Jacques Lacapère
Author: Isabel Moraes
Author: Julia Koehler Leman
Author: Xin Gao
Author: Hartmut Michel
Author: 
Author: Christophe Chipot