Thermostable Proteins

Thermostable Proteins: Structural Stability and Design

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Features

  • Devoted to the understanding of the physical origin of thermal stability of thermophilic proteins and survival mechanisms of thermophilic life forms
  • Covers the design of thermophilic proteins without affecting their original functions
  • Includes color inserts to aid in the understanding of structural stability and designing of proteins

Summary

Thermostable Proteins: Structural Stability and Design provides a comprehensive, updated account of the physical basis of enhanced stability of thermophilic proteins and the design of tailor-made thermostable proteins, paving the way for their possible industrial applications. This book is devoted to understanding the survival mechanisms of "thermophilic life forms" at the molecular level with an emphasis on design strategies.

The review chapters presented in Thermostable Proteins span a wide range of protein thermostability research. Basic structural, thermodynamic, and kinetic principles are explained and molecular strategies for the adaptation to high temperatures are delineated. In addition, this book covers:

  • Computing and simulation methods in current and future thermostability research, especially in nonempirical situations
  • How rigidity theory is used to improve the thermal adaptation of mesophiles
  • Subtilisin-like serine proteases and their significant engineering applications
  • The state of knowledge concerning structure–function relations and the origins of their structural stability
  • Computational and experimental approaches for the design of proteins with increased thermal stability based on sequences or three-dimensional structures

Understanding the molecular basis of how thermostable and hyperthermostable proteins gain and maintain their stability and biological function at high temperatures remains an important scientific challenge. A more detailed knowledge of protein stability not only deepens our understanding of protein structure but also helps in obtaining insights into processes that drive protein activities—folding, unfolding, and misfolding—essential to biological function.

Table of Contents

Delineation of the Conformational Thermostability of Hyperthermophilic Proteins Based on Structural and Biophysical Analyses
Atsushi Mukaiyama and Kazufumi Takano
Role of Packing, Hydration, and Fluctuations on Thermostability
Fabio Sterpone and Simone Melchionna
Analyzing Protein Rigidity for Understanding and Improving Thermal Adaptation
Doris L. Klein, Sebastian Radestock, and Holger Gohlke
Thermostable Subtilases (Subtilisin-Like Serine Proteinases)
Magnús M. Kristjánsson
Combined Computational and Experimental Approaches to Sequence-Based Design of Protein Thermal Stability
Julie C. Mitchell, Thomas J. Rutkoski, Ryan M. Bannen, George N. Phillips, Jr.
Designing Thermophilic Proteins: A Structure-Based Computational Approach
Sohini Basu and Srikanta Sen
Index

Editor Bio(s)

Dr. Srikanta Sen is currently working as a Senior Fellow at Chembiotek, a TCG Life Sciences group of companies in India. He has developed the Molecular Modeling and Computational Biology group of Chembiotek and has been leading the group for the last ten years. He received his M.Sc. degree in physics from Calcutta University, India. He pursued his Ph.D. work at the Theory Division of Saha Institute of Nuclear Physics, Calcutta and received his Ph.D. degree in Physics in 1991 from Calcutta University. He did his post-doctoral research between 1992 – 1998 at Umea University, Stockholm University and Karolinska Institute in Sweden. He then worked in Indian Institute of Chemical Biology in Calcutta, India for two years. He moved over to Chembiotek in 2001.

His research interest includes application of statistical mechanics to biomolecular systems; molecular modeling based investigations of structural, dynamical and interactional behaviors of biomolecules and their complexes; protein design; pharmacophore modeling; molecular docking and virtual screening of compounds to find leads in drug discovery projects; drug design; as well as QSPR based prediction of properties of compounds from their structures. He has also developed many computational tools to facilitate the research work of his group.

Prof. Lennart Nilsson is currently working at Karolinska Institutet, Stockholm, Sweden, where he leads a research group in Molecular Modeling since 20 years. He obtained his M.Sc. degree in engineering physics as well as his PhD in theoretical physics (1983) from the Royal Institute of Technology, Stockholm. He did his post-doctoral research 1983-1984 at Harvard University.

His research interests include protein-nucleic acid interactions, especially transcription factors and the ribosome, and questions concerning information transfer in biomolecular complexes. He is one of the core developers of the CHARMM molecular simulation program.

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