Physical Principles and Techniques of Protein Chemistry, Part 2Sydney J. Leach, Sidney J. Leach Physical Principles and Techniques of Protein Chemistry, Part B deals with the theories and application of selected physical methods in protein chemistry evaluation. This book is divided into seven chapters that cover the ultracentrifugal analysis, light scattering, infrared (IR) methods, nuclear magnetic resonance (NMR) spectroscopy, and differential thermal analysis of protein properties. This text first describes the fundamental ideas and methodology of sedimentation analysis of ideal noninteracting solutes and the problems of nonideality and solute-solute interaction. This book then deals ... |
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Page 118
... length when com- pletely stretched out , and also by its persistence length q , defined as the mean value of the projection , along the direction of its first segment , of an infinitely long molecular chain . Thus , a stiff chain will ...
... length when com- pletely stretched out , and also by its persistence length q , defined as the mean value of the projection , along the direction of its first segment , of an infinitely long molecular chain . Thus , a stiff chain will ...
Page 119
... length ( r2 ) av1 / 2 , where r is the end - to - end - length in a particular conforma- tion and the averaging process is over the squares of all possible values of r . Another related quantity , which can be estimated directly from ...
... length ( r2 ) av1 / 2 , where r is the end - to - end - length in a particular conforma- tion and the averaging process is over the squares of all possible values of r . Another related quantity , which can be estimated directly from ...
Page 230
... length must be capable of very finely controlled adjustment . Matched , fixed , path length cells are not suitable because the protein occupies a significant proportion of the cell volume . If a protein of specific volume v ml / gm in ...
... length must be capable of very finely controlled adjustment . Matched , fixed , path length cells are not suitable because the protein occupies a significant proportion of the cell volume . If a protein of specific volume v ml / gm in ...
Contents
Ultracentrifugal Analysis | 10 |
Light Scattering | 12 |
Osmotic Pressure | 13 |
Copyright | |
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absorption acid angle axial ratio axis band beam binding Biol Bradbury Brice calculated capillary centrifugal chain Chem chemical shifts column complex component concentration dependence constant copper(II denaturation density gradient determined diffusion dilution Doty effect ellipsoid equation experiments extrapolation filters Fraser frequency fringe groups Gurd Holtzer hydrogen increment instrument interaction intrinsic viscosity Kirkwood length light scattering light-scattering linear macromolecule maximum measured meniscus method molecular weight molecule Natl observed obtained optical density optical system parameters partial specific volume particle peak photographic Phys plate plateau plot Polymer Sci Proc procedure protein solution protons radius random coil Rayleigh reference refractive index refractive index increment residues resonance rotation rotor sample Schachman schlieren Section sedimentation coefficient sedimentation equilibrium shearing stress shown in Fig slit solvent spectra spectrum speed structure synthetic boundary Tanford technique temperature Timasheff tion transmittance tube ultracentrifuge values Vinograd viscometer zero Zimm zone