Physical Principles and Techniques of Protein Chemistry, Part 1Sydney J. Leach Physical Principles and Techniques of Protein Chemistry, Part A deals with the principles and application of selected physical methods in protein chemistry evaluation. This book is organized into nine chapters that cover microscopic, crystallographic, and electrophoretic techniques for protein conformational perturbations evaluation. This text first presents a general account of electron microscopy, its specimen preparation, optimum conditions for high resolution, measurement of electron micrographs, and illustrative examples of protein study. This book then examines the different types of map ... |
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Page 304
... DISTRIBUTION OF RELAXATION TIMES In the discussion presented hitherto , it is tacitly assumed that the dielectric relaxation is characterized by only one relaxation time . The theory described above is therefore referred to as the Debye ...
... DISTRIBUTION OF RELAXATION TIMES In the discussion presented hitherto , it is tacitly assumed that the dielectric relaxation is characterized by only one relaxation time . The theory described above is therefore referred to as the Debye ...
Page 305
... distribution functions to explain the distribution of relax- ation times . However , the results are not satisfactory and it is generally believed that empirical methods are more useful . The empirical method which has been used most ...
... distribution functions to explain the distribution of relax- ation times . However , the results are not satisfactory and it is generally believed that empirical methods are more useful . The empirical method which has been used most ...
Page 398
... distribution can be expressed in terms of the moments of the gradient curve x " taken about the centroidal axis ∞ 9 ( 4 ) = [ 1/8 ( 2w ) 1 / ? ] ( exp −μ ° / 28 ° ) { 1 + Σ HK - - k = 3 - Ck k ! } ( — i ) * a * H2 [ iμo / Et ̧2α ] ...
... distribution can be expressed in terms of the moments of the gradient curve x " taken about the centroidal axis ∞ 9 ( 4 ) = [ 1/8 ( 2w ) 1 / ? ] ( exp −μ ° / 28 ° ) { 1 + Σ HK - - k = 3 - Ck k ! } ( — i ) * a * H2 [ iμo / Et ̧2α ] ...
Contents
Electron Microscopy of Globular Proteins | 2 |
Ultraviolet Absorption | 3 |
The Enhancement of Contrast | 21 |
Copyright | |
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absorption absorption spectrum applied atoms axis Biochem Biol Biophys birefringence boundary bovine serum albumin buffer calculated Cann Chem chromophores coefficient components concentration curve denaturation density determined dielectric constant dielectric increment dielectric relaxation difference spectrum diffraction dipole moment Edelhoch effects electric birefringence electric field electron microscope electrophoresis elution volume emission enzyme equation equilibrium excitation experimental factor film fluorescence fraction frequency gel filtration gradient groups intensity interactions ionic strength ions lens light linear macromolecules measured method micrographs migration mobility molar molecular weight molecules moving-boundary observed obtained optical ovalbumin parameter particles peaks permanent dipole perturbation phase phenolic photomultiplier Phys plot polarization polymer produced protein quantum yield ratio reaction relaxation residues resolution resolving power ribonuclease scattering shadow shown in Fig solution solvent specimen spectra structure studies technique temperature theoretical theory tion tryptophan tyrosine unit cell values wavelength Weber Winzor zone